NAPHTHALENE
Ambient Water Quality Criteria
             Criteria and Standards Division
             Office of Water Planning and Standards
             U.S.  Environmental Protection Agency
             Washington,  D.C.

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                        CRITERION DOCUMENT              r _ _

                                                        C25639
                           NAPHTHALENE


CRITERIA


                           Aquatic Life


     For freshwater aquatic life, no criterion for napthalene can


be derived using the Guidelines, and there are insufficient data


to estimate a criterion using other procedures.


     For saltwater aquatic life, no criterion for naphthalene can


be derived using the Guidelines, and there are insufficient data


to estimate a criterion using other procedures.


                           Human Health


     For the protection of human health from the toxic properties


of naphthalene  ingested through water and through contaminated


aquatic organisms, the ambient water criterion is determined to be


143 ug/1.

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                         NAPHTHALENE
Introduction
     Naphthalene is the most abundant single constituent
of coal tar  (Schmeltz, et al. 1977).  In 1974, 1.8 x 10
metric tons of naphthalene were produced from coal tar,
and 1.1 x 105 metric tons were produced from petroleum  (Brown,
et al. 1975; U.S. EPA, 1976).  This compound is used as
an intermediate in the production of dye compounds and  the
formulation of solvents, lubricants, and motor fuels.   One
of the principal uses of naphthalene as a  feedstock in  the
United States  is for the synthesis of phthalic anhydride.
It has also  been used directly as a moth repellant and  insec-
ticide as well as an antihelminthic, vermicide, and an  intes-
tinal antiseptic.
     Napthalene  is a bicyclic aromatic  hydrocarbon with
the chemical formula C10HQ and a molecular weight of 128.16.
Pure naphthalene forms a white crystalline solid at room
temperature  whereas the crude or technical grades may  range
in color  from  brown to tan.  Naphthalene vapor  and dust
can  form  explosive mixtures  with air  (Windholz,  1976).
      Pure naphthalene melts  at 80.2°C;  the less  pure  forms
of the  compound  will  melt  at temperatures  ranging  from 74
to 80°C.   The  boiling  point  of naphthalene is  217.96°  at
atmospheric pressure  (Manufacturing Chemists Assoc.  1956) .
At  15.5°C,  the density is  1.145  (Manufacturing  Chemists
Assoc.  1956) and at 100°C  the  density is  0.9625 (Marti,
 1930;  Weast, 1975).   At  19.8°C the vapor  pressure  of  solid
 naphthalene is 0.0492 mm Hg  (Gil'denblat,  et al.  1960).
                               A-l

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     The  solubility  of  naphthalene  in  water  has  been reported
to range  between  30,000 /ig/1  (Mitchell,  1926)  and  40,000
jug/1  (Josephy  and Radt, 1948)  at  25°C.   The  solubility of
naphthalene  in seawater will  vary according  to the degree
of chlorosity;  in seawater of average  composition  the solu-
bility of naphthalene is  approximately 33,000 jug/1 (Gordon
and Thorne,  1967).   Naphthalene has also been  reported to
be soluble in  organic solvents (Spector, 1956).
     Naphthalene  can oxidize  in the presence of  light and
air, and  it  was determined that 50  percent of  the  theoretical
CO2 was liberated after 14 days  (Ludzack and Ettinger, 1963).
The process  involves initial  conversion to naphthaquinone
with subsequent rupture of one of the  aromatic rings and
the release  of CO2  (Kirk  and  Othmer, 1967).  However, this
oxidation process occurs  only at  elevated temperatures (Josephy
and Radt, 1948).
     When combined with alcohol and ozone, cyclic  alkoxy-
hydroxyperoxides  are formed.   In  an acidic medium, these
peroxides will be converted to methyl  phthalaldehydate;
in a basic medium, they are converted  to phthalaldehydic
acid (Bailey,  et  al.  1964).   When  combined  with metal nitrate
within a  temperature range of 55°C  to  180°C, naphthalene
can be nitrated at the  alpha  position  (Alaraa and Okon, 1964).
In the presence of oxygen, K2SO4/ a vanadium oxide catalyst,
and SiO4,  naphthalene can be  converted to phthalic anhydride
(Morotskii and Kharlampovich,  1968).
     Microorganisms can degrade naphthalene  to 1,2-dihydro-
1,2,-dihydroxynaphthalene and ultimately to  carbon dioxide
                               A-2

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and water.  Studies have indicated a degredation rate  under
laboratory conditions of up to 3.3 ug/1  (Lee and Anderson,
1977).
     Naphthalene has been shown  to be  toxic to microorganisms
and has been reported to reduce  photosynthetic rates in  algae.
It has also been reported to be  acutely  toxic to various
invertebrate and vertebrate species of aquatic organisms.
In laboratory mammals and humans, naphthalene has been linked
to blood disorders and  is suspected of traversing the  placental
membrane  in humans following naphthalene ingestion  by  the
mother.
     Naphthalene has a  varied environmental distribution
and has been detected  in ambient water  (up to 2.0 jug/1),
sewage plant effluents  (up  to 22 jig/I),  and drinking water
supplies  (up to 1.4 jug/1)  (U.S.  EPA,  1971-1977).  Recent
studies have determined that naphthalene will accumulate
in sediments by more than 100 times  the  concentration  in
the overlying  water  (Cox, et al. 1975;  Lee and Anderson,
1977).
      Naphthalene has been shown  to  bioconcentrate  in  both
invertebrate and vertebrate species  of aquatic organisms.
It has also been suggested  that  much of  the  naphthalene
taken up  by aquatic organisms returns to the  ecosystem in
fecal matter without  being  metabolized.   In  addition,  in
vitro studies  have identified  three  naphthalene  metabolites
derived from rat  liver microsome preparations;  these  probably
resulted  from  hydroxylation and  conjugation  with water-soluble
moieties.
                               A-3

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                          REFERENCES

Alaraa, W.,  and K. Okon.   1964. Direct  nitration  of  benzene,
naphthalene,  and phenol by  inorganic nitrates.   Buil. Wojskowa
Akad. Tech. 13: 51.

Bailey,  P.S., et al.  1964.  Ozonolysis of  naphthalenes;
the  aromatic  products.  Jour. Org.  Chem. 29:  697.

Brown, S.L.,  et al.  1975. Research  program on hazard priority
ranking  of  manufactured chemicals.  Phase  II  - Final Report,
A report prepared by Stanford Research Institute.   National
Science  Foundation,  Washington, D.C.   pp.  62-A-l.

Chemical Economics Handbook. 1976.  Chem.  Inf. Serv., Stanford
Res. Inst., Menlo Park, Calif.

Cox, B.A.,  et al. 1975. An  experimental oil spill:  The
distribution of aromatic hydrocarbons  in the  water, sediment,
and animal  tissues within a shrimp  pond.   Iri  Proc.  Conf.
Prevent. Control Oil Pollut. San Francisco, March 25-27,
1975.  Am. Petrol.  Inst., Washington,  D.C.

Gil'denblat, I.A.,  et al. 1960.   Vapor  pressure over crystal-
line naphthalene.   Jour. Appl.  Chem. USSR.  33: 245.
                               A-4

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Gordon, J.E., and R.L. Thome. 1967.  Salt effects on non-



electrolyte solutions.  Geschim.  Cosmochim. Acta.  31:



2433.







Josephy, E., and F. Radt, eds. 1948.  Encyclopedia of organic



chemistry:  Series III.  Elsevier Publishing Co., Inc.,



New York.







Kirk,  R.E., and D.F.  Othmer.  1967.  Encyclopedia of chemical



technology. 2nd ed.   John Wiley and Sons, Inc, New York.







Lee, R.F.,  and J.W. Anderson.  1977.  Fate and effect of



naphthalene:  Controlled ecosystem pollution experiment.



Bull.  Mar.  Sci.  27: 127.







Ludzack,  F.J., and M.B. Ettinger. 1963.  Biodegradability



of  organic  chemicals  isolated from  rivers.  Purdue Univ.



Eng. Bull.  Ser.  No.  115:  278.







Manufacturing  Chemists Assoc.  1956.   Chemical  safety data



 sheets SD-58:   Naphthalene. Washington,  D.C.







Marti, F.B. 1930.   Methods and equipment used  at the Bureau



 of Physiochemical Standards.  Bull.  Soc. Chim.  Bedgrad.



 39: 590.
                               A-5

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 Mitchell,  S.  1926.   A method for- determining the solubility
 of  sparingly  soluble substances.  Jour.  Chem.  Soc.  129:
 1333.

 Morotskii, O.A.,  and G.D.  Kharlampovich.  1968.   Phthalic
 anhydride.  Izobret., Prom.  Obraztsy,  Tovarnye  Znaki.  45:
 22.

 Schmeltz,  I., et  al. 1977.   The role  of  naphthalenes  as
 carcinogens.   A paper presented at the 16th Annu. Meet.
 Soc. Toxicol. Toronto, Can.  March 27-30,  1977.

 Spector, W.S., ed.  1956.   Handbook of  toxicology.   Saunders
 Publishing Co., Philadelphia.

 U.S. EPA.  1971-1977.  Unpublished data from Region  IV, Atlanta
 Ga.

 U.S. EPA.  1976.  Organic chemical producer's data base program.
 Chemical No.  2701.   Radian Corporation.

Weast,  R.C. 1975.   Handbook  of  chemistry  and physics.  CRC
 Press,  Cleveland,  Ohio.

Windholz, M., ed.  1976.  The Merck Index. 9th ed. Merck
and Co., Rahway, N.J.
                              A-6

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AQUATIC LIFE TOXICOLOGY*



                       FRESHWATER ORGANISMS



Introduction



     A limited variety of aquatic species  has  been  exposed  to



naphthalene and all tests were under  static procedures with



unmeasured test concentrations.  Fifty percent  effect levels are



in the range of 5,600 to 82,000 ug/1.  One embryo-larval  test with



the fathead minnow demonstrated no  adverse effects  at the highest



test concentration of 440 ug/1.



Acute Toxicity



     The adjusted 96-hour LC50 value  for the mosquitofish (Wallen,



et al. 1957) is 82,000 ug/1  (Table  1) and  after division  by the



species sensitivity factor  (3.9) results in a  Final Fish  Acute



Value of 21,000 ug/1.



     Daphnia magna appears  to be more sensitive with an adjusted



48-hour EC50 of 7,260 ug/1  (Table 2).  Based on this single datum,
*The reader  is  referred  to  the Guidelines  for Deriving Water



Quality Criteria for  the Protection of Aquatic  Life  [43  FR  21506



(May 18, 1978)  and  43 FR 29028  (July  5,  1978)]  in order  to  better



understand the  following discussion and  recommendation.  The



following tables contain the  appropriate data that were  found  in



the literature, and at the  bottom of  each  table are  the  calcula-



tions for deriving  various  measures of toxicity as described  in



the Guidelines.
                             B-l

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the Final Invertebrate Acute Value for naphthalene  is  350  ug/1.
Since this concentration  is lower than the equivalent  value  for
fish, 350 ug/1 is also the Final Acute Value.
Chronic Toxicity
     Exposure concentrations as high  as  440  ug/1  (Table  3} caused
no adverse effects on survival or growth during an  embryo-larval
test with the fathead minnow (U.S. EPA,  1978).  This datum results
in a Final Fish Chronic Value that is greater  than  33  ug/1.   No
chronic data for  invertebrate species are available.
Plant Effects
     A 50 percent reduction  in the number of cells  of  the  alga,
Chlorella vulgaris,  occurred at a concentration of  33,000  ug/1
 (Table 4).  This  concentration is the Final  Plant Value.
Residues
     No measured  steady-state bioconcentration factor  (BCF)  is
available for naphthalene.  A BCF can be estimated  using the
octanol-water partition  coefficient  of  2,300.   This coefficient  is
used to derive an estimated  BCF of 210  for aquatic  organisms that
contain about 8 percent  lipids.   If  it  is known that  the diet of
the wildlife of concern  contains a significantly  different lipid
content, an appropriate  adjustment  in the estimated BCF should  be
made.
Miscellaneous
     Soto, et al. (1975a) observed the  death of 61  percent of the
cells of the alga, Chlamydomonas angulosa,  at  a concentration of
34,400 ug/1 (Table 5).  There was a  50  percent mortality of  coho
salmon after an exposure  of less than six hours to  5,600 ug/1
 (Holland, et al.  1960) .
                              B-2

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CRITERION FORMULATION
                     Freshwater Aquatic Life
Summary of Available Data
     The concentrations below have been rounded to  two significant
figures.
     Final Fish Acute Value = 21,000 ug/1
     Final Invertebrate Acute Value =  350 ug/1
          Final Acute Value = 350 ug/1
     Final Fish Chronic Value = greater than  33 ug/1
     Final Invertebrate Chronic Value  = not available
     Final Plant Value = 33,000 ug/1
     Residue Limited Toxicant Concentration = not available
          Final Chronic Value = greater than  33 ug/1
          0.44 x Final Acute Value » 150 ug/1
     No  freshwater  criterion can be derived for napthalene  using
the Guidelines because no  Final Chronic Value for either  fish  or
invertebrate species or a  good substitute for either value  is
available, and there are insufficient  data  to estimate a  criterion
using other procedures.
                              B-3

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CD
I
*»
                     Table  1.   Freshwater fish acuta values for naphthalene (Wallen, et al. 1957)


                                                                       Adjuaced
                               Bloaaoay  Teat      Time      LC50      LCSO
                                                   Qtraj      ("9/^t     fug/1) __
       Hoaqultofish.              S        U        96      150,000    82,000
       Cambuaia afflnla
       *  S - static

       ** U • unmeasured
                                                    i '
          Geometric mean of adjusted  values - 82.000 iig/1;  ii^-^ - 21*000  ng/l

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                        Tuble  2.  1'reshwater Invertebrate  acute values for naphthalene (U.S. EPA.  1978)


                                                                            Adjusted

                                  lUcussay   Test       Time      LC50       I.CiiO
                                  tlEli!t>!J*._   Cone ,**    (tub)      (u>|/t)     (
         Cladoceran.                 S        U         48        8,570      7.260
         Dapjinl a mapna
         *  S *» static

         ** U «• unmeasured

            Geometric mean  of adjusted  values •»  7,260 ug/l,'    ~2T^ "  35°
 I
tn

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                      Table  3.  Freshwater fish chronic values for naphthalene  (U.S. EPA, 1978)


                                                         Chronic
                                               Limits    Value
                                     Ifist*      lug/l)     440      >220
        pjmcphalas promelaa



        * E-L - embryo-larva

          Geometric mean of chronic  values -  >220  iig/1,'   >|^j -  >33  ng/1

          Lowest chronic value - >220 \ig/l
00

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33
I
                        Table  A.   Freshwater plane effects for naphthalene (Kauss & llutchlnaon,  1975)
                                                 Concentration
          Otgdniain                Etfect         (ug/ij	
          Alga.                    EC50 48-hr        33,000
                                  cell numbers
          Final plant value - 33.000 ng/l

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03
I
00
                           Table  S.   Other freshwater data for naphthalene
                                Teat
                                           FttSfft
                                                                   Result
Alga,
        Alg
          '
Alga,
Chlamydomonaa anguloaa

Col 10 salmon,
Oncurhynchua kiautch
24 hra


24 hra


<6 hra
Death of 6IX of calls    34,400    Soto, et al.  1975a
                                          Loaa of photosynthetlc     10%     Soto, et al.  1975b
                                          capacity                aaturatlon
                                          50% mortality
                          5,600    Holland, et al.  1960

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                       SALTWATER ORGANISMS
Introduction
     As with freshwater organisms,  the data  base  for  napthalene
and saltwater organisms is limited  to a  few  species for  which
static test procedures were used with measured  concentrations.   A
variety of adverse effects were observed  at  concentrations  of
1,000 to 2,600 ug/1-
Acute Toxicity
     The adjusted 96-hour LC50 value  for the sheepshead  minnow was
1,125 ug/1  (Anderson, et al.  1974)  and  this  result provides a
Final Fish Acute Value of 300 ug/1  (Table 6).
     Anderson, et al.  (1974)  also exposed grass and brown shrimp
for  24 hours  to napthalene  and  these  data provide adjusted LC50
values of  744  and 715 ug/1/  respectively (Table 7).   Tatem (1976)
tested the  grass  shrimp  (Palaemonetes pugio) and this result leads
to an  adjusted LC50  of  2,585  ug/1.   The  geometric mean of these
data is  996  ug/1  and after  division by the sensitivity factor
 (49),  a  Final Invertebrate  Acute  Value of 20 ug/1 is  derived.
This also becomes the Final Acute Value since 20 ug/1 is lower
than the Final Fish  Acute Value of  300 \ig/l.
Chronic  Toxicity
      No  data are  available  on the chronic effects of naphthalene
on saltwater organisms.
                              n-9

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Residues
     There is only one test result  (Harris,  et  al.  1977b)  that
determined an apparent equilibrium  bioconcentration  factor (BCF)
for napthalene.  After nine days, the BCF  for a copepod was.5,000
(Table 8).  Data for other species  for exposures  of  one hour  to
one day are listed in Table 9.  These BCF's  range  frcm 32  to  77
and indicate  that equilibrium does  not occur rapidly when  those
results are compared to  the BCF of  5,000 after  nine  cays.
Miscellaneous
      Berdugo,  (1977) exposed  the  copepod  (Eurytemora affinis)  to  a
concentration of 1,000 ug/1 and observed effects  on  egg production
and  ingestion rate.
                              n-10

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CRITERION FORMULATION



                      Saltwater Aquatic Life



Summary of Available Data



     The concentrations below have been rounded  to  two  significant




figures.



     Final Fish Acute Value = 300 ug/1



     Final Invertebrate Acute Value = 20 ug/1



          Final Acute Value = 20 ug/1



     Final Fish Chronic Value = not available



     Final Invertebrate Chronic Value = not available



     Final Plant Value = not available



     Residue Limited Toxicant Concentration =  not available



          Final Chronic Value = not available



          0.44 x Final Acute Value =8.8 ug/1



     No  saltwater  criterion can be derived for napthelene  using



the Guidelines because no  Final Chronic Value  for either  fish  or



invertebrate species or a  good substitute for  either value is



available, and there are insufficient data to  estimate  a  criterion




using other procedures.

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•a
i
M»
to
                          Table  6.   Mairlno  flbh  acute  values  for naphthalene (Anderson, et al. 1974)



                                                                             Adjusted
                                    Bioaaaay  Teat      Time       LC&O      LC50
                                    B££l)Sd*_  Cone t **    (lira)
            Shcepshead minnow,         S        H         2^i       2,AGO      1.125
            Cy^ri^noJou yarie^atua
            * S - utatic


            *»M <* measured.


              Coometrlc mean of adjusted  values -  1,125  i
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              Tab it:  7.   Marine invertebrate acute values  for naphthalene
QlUiiQiiB
biousaay  Test       Time
M£iiiSsU_  Cgnc .**
                                                        ijCSO
                                         Adjusted
                                         LCbO
[.fetet encfc
Grass shrimp, S M 24
i'aiaemoneteti pugiu
Crass shrimp. S M 96
Palaonionetca pufiio
Brown ahrimp, S M 24
Penaeus aztecua

* S - static
** M • measured
Geometric mean of adjusted values » 996 ug/1 \
03
u>
2,600 744 Anderson, et al. 1974
2.350 2,585 Tatem, 1976
2,500 715 Anderson, et al. 1974
996 - 20 ug/l

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03
I
                       Table  8.  Marine residues for napchalene   (Harris, et al. 1977b)

                                                                         Time
         ortiant§a                          Biocopcentration  Factoi *    (days)

         Copcpod,                                 5,000                   9
         Eurytemora afflnla
           Dry weight Co wet weight conversions.

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Table  9.  Other marine data for napthalene
Organism
Copepod.
Eiirytemora af finis
Copepod,
Eurytemora afftnia
Copepod ,
Calanua helgolondtcus
Copepod,
Calanus helgolandicus .
Blue mussel,
Mytilus edults
Sand goby.
0-, Cillichtus mirabills
1
•-1 Sculpin,
PlJRocottus maculoaua
Saitd dab,
Cttharichtys attftmaeus
Test
0.16 days
1 day
1 day
1 day
A hrs
1 hr
3 hrs
1 hr
Etteft
Reduction In ingestion
rate of 101 (P - 0.05)
Reduction in egg
production by 83%
(P - 0.05)
Bioconcentration
factor - 50
Bioconcentration
factor - 60
Bioconcentration
factor - AA
Bioconcentration
factor - 63
Bioconcentration
factor - 32
Bioconcentration
factor • 77
Result
JiUI^U.
1,000
1.000
-
-
-
                                                  Berdugo, 1977





                                                  Berdugo, 1977







                                                  llarria, et al.  1977b





                                                  Harris, et al.  1977a





                                                  Lee,  et al. 1972b





                                                  Lee,  et al. 1972a





                                                  Lee,  et al. 1972a





                                                  Lee,  et al. 1972a

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                          REFERENCES

Anderson, J.W.,  et  al.   1974.  The  effects  of  oil  on  estuarine
animals:  toxicity,  uptake  and depuration,  respiration.
In  Pollution and physiology of marine  organisms.   Academic
Press,  Inc.  New  York.

Berdugo, V.   1977.   The  effect of petroleum hydrocarbons
on  reproduction  of  an  estuarine  planktonic  copepod in labora-
tory cultures.   Mar. Pollut.  Bull.   8:  138.

Harris, R.P., et al.   1977a.  Factors  affecting the retention
of  a petroleum hydrocarbon  by marine planktonic copepods.
In  Fate and  effects of petroleum hydrocarbons  in marine
ecosystems and organisms.   Proc. Symp.  286.

Harris, R.P., et al.   1977b.  Accumulation  of  carbon-14-
1-napthalene by  an  oceanic  and an estuarine  copepod during
long-term exposure  to  low-level  concentrations.  Mar.  Biol.
42:  187.

Holland, G.A., et al.  1960.  Toxic  effects  of organic and
inorganic pollutants on young salmon and trout.  Wash.
Dep. Fish.  Res.  Bull.  5: 162.
                              B-16

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Kauss, P.B., and T.C. Hutchinson.  1975.  The effects of



water-soluble petroleum components on the growth of Chlorella



vulgaris Beijerinck.  Environ. Pollut.  9: 157.







Lee, R.F., et al.  1972a.  Uptake, metabolism and discharge



of polycyclic aromatic hydrocarbons by marine fish.  Mar.



Biol.  17: 201.







Lee, R.F., et al.  1972b.  Petroleum hydrocarbons:  uptake



and discharge by the marine mussel Mytilus edulis.  Science



177: 344.







Soto, C.,  et al.  1975a.  Effect of naphthalene and aqueous



crude oil  extracts on the green  flagellate Chlamydomonas



angulosa.   I. Growth.  Can. Jour. Bot.  53:  109.







Soto, C.,  et al.  1975b.  Effect of naphthalene and aqueous



crude oil  extracts on the green  flagellate Chlamydomonas



angulosa.   II.  Photosynthesis  and uptake  and release of



naphthalene.  Can. Jour. Bot.  53: 118.







Tatem, H.E.  1976.   Toxicity  and physiological  effects of



oil  and  petroleum hydrocarbons on estuarine grass  shrimp



Palaemonetes pugio Holthuis.   PhD dissertation.  Texas A



&  M  University.  133 pp.
                               B-17

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U.S. EPA.  1978.  In-depth studies on health and environmental



impacts of selected water pollutants.  U.S. Environ. Prot.



Agency, Contract No. 68-01-4646.







Wallen, I.E., et al.  1957.  Toxicity to Gambusia affinis



of  certain pure chemicals in turbid waters.  Sewage Ind.



Wastes  29: 695.
                               B-18

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Mammalian Toxicology and Human Health Effects
                           EXPOSURE
Introduction
     Naphthalene, cinH8f ^s an aromatic hydrocarbon with
two orthocondensed benzene rings.   In 1965,  74.4 percent
of the napthalene produced in this  country was  used for
the manufacture of phthalic anhydride which,  in turn, was
used in the manufacture of alkyd  and polyester  resins, dyes,
pigments, Pharmaceuticals and insecticides:  12.2 percent
was used  in the manufacture of  insecticides  such as 1-naphthyl-
N-methylcarbamate  (carbaryl); 11  percent  was used  for the
production of  2-naphthol  (used  as a dyestuff,  pigment and
pharmaceutical intermediate)  and  mothballs.   The remainder
was used  in the manufacture of  alkyl-naphthalenesulfonates
 (used  in  the manufacture of detergents  and  textile wetting
agents) ,  alkylnaphthalenes  (used  in making  textile spinning
lubricants), chlorinated naphthalenes  and tetra and decahydro
naphthalenes  (used in solvent mixtures).   In 1965, the  total
U.S. production of naphthalene  was 373,000  metric  tons  while
 in 1976  production of petroleum derived naphthalene was
 48,720 metric  tons.
      In 1973,  91 percent of  the production was from petroleum
 while  the remainder originated  from coal tar distillates.
 In 1974,  35 percent was from petroleum while 58 percent
 was from coal tar distallates  originating from the high
 temperature coking of bituminous coal (Brown, et al.  1975;
 U.S.  EPA, 1976).  This coal tar naphthalene in its crude
 state contains impurities such  as alkylnaphthalenes,

                               C-l

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alkylcoumarones and thianaphthene.  This  latter  impurity
has been hypothesized as being  the active ingredient  in
moth balls  (Thiessen, 1967).
     Pure naphthalene melts at  80.29°C. and boils  at  217.955°C,
It has a high vapor pressure  (0.054 mmHg  at 20°C.) and high
water solubility  (19,000 jug/1 at 0°C and  30,000 jug/1  at
100C.) compared to other polynuclear aromatic hydrocarbons.
                              C-2

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Ingestion from Food and Water
     The two major sources  of  naphthalene  in the  aquatic
environment are from  industrial effluents  and from oil spills.
Industrial effluents  have been found to have up to 32,000
jug/1 naphthalene.  The  final effluents of  sewage treatment
plants receiving discharges from these facilities have been
noted to have  up to  22  ug/1 naphthalene. Natural waters
have been noted  to have up  to 2.0 ug/1 of  naphthalene while
drinking water supplies have been found to have up to 1.4
ug/1 naphthalene  (U.S.EPA,  Region IV, unpublished data).
     A bioconcentration factor  (BCF) relates the concentra-
tion of  a chemical in water to  the concentration in aquatic
organisms,  but BCF's are not available  for  the edible por-
 tions  of all four  major groups  of aquatic organisms consumed
 in the United States.  Since data indicate  that  the BCF
 for lipid-soluble compounds is  proportional to percent lipids,
 BCF's  can be adjusted to edible portions  using data on per-
 cent lipids and the  amounts of  various  species consumed
 by Americans.  A  recent  survey  on fish  and  shellfish  consump-
 tion in the United States  (Cordle,  et al. 1978)  found that
 the per capita consumption is 18.7  g/day.   From the  data
 on the nineteen major  species identified  in the survey and
 data on the fat content  of the edible portion of these spe-
 cies  (Sidwell, et al.  1974),  the relative consumption of
 the four major groups  and  the weighted average percent lipids
 for each group  can  be  calculated:
                                 C-3

-------
                     Consumption       Weighted Average
        Group          (Percent)         Percent Lipids
Freshwater fishes        12                   4.8
Saltwater fishes         61                   2.3
Saltwater molluscs        9                   1.2
Saltwater decapods       18                   1.2
Using the percentages  for consumption  and  lipids  for each
of these groups,  the weighted  average  percent lipids is
2.3  for consumed  fish  and shellfish.
     No measured  steady-state  bioconcentration factor,  (BCF)
is available  for  naphthalene,  but  the  equation "Log BCF
= 0.76 Log P  -  0.23" can be  used  (Veith, et  al. Manuscript)
to estimate the BCF  for aquatic organisms  that contain about
eight percent lipids from the  octanol-water  partition coef-
ficient  (P) .   Based on an octanol-water partition coefficient
of 2,300, the steady-state bioconcentration  factor for naptha-
lene is estimated to be 210.   An adjustment  factor of 2.3/8.0
= 0.2875 can  be used to adjust the estimated BCF  from the
8.0 percent lipids on  which  the equation  is  based to the
2.3 percent lipids that is the weighted average for consumed
fish and shellfish.  Thus, the weighted average bioconcentra-
tion factor for napthalene and the edible  portion of all
aquatic orgnisms  consumed by Americans is  calculated to
be 210 x 0.2875 = 60.
Inhalation
     Unusual  exposure  to naphthalene can occur to cigarette
smokers, naphthalene being identified  as one of the polynu-
clear aromatic  hydrocarbons  found  in cigarette smoke conden-
                               C-4

-------
sate (Akin, et al. 1976).  Under-industrial conditions indivi-
duals can be exposed to levels of naphthalene up to 1.1
x 10 /ag/m  (210 ppm) as vapor and  up  to  4.4 jug/m  as particu-
lates (Table 1).  Potential exposure categories in this
group are outlined in Table 2.  Ambient air levels of naph-
thalene are negligible  (Table 1), but  the number of measure-
ments have been limited.
Dermal
     Data on dermal exposure to naphthalene are very sparse.
See the "Effects" section  for discussion  of effects from
possible dermal exposure.
                       PHARMACOKINETICS
Absorption, Distribution and Excretion
     Little detailed information  is available on the absorp-
tion, distribution or excretion of  naphthalene  in man or
animals.  Adequate amounts of naphthalene can be absorbed
when ingested  as  a solid to cause toxicity  in man  (Chusid
and Fried, 1955;  Zuelzer and Apt,  1949; Nash, 1903; Gross,
et al. 1958; Haggerty,  1956). When  taken  as  a solid, frag-
ments of naphthalene can appear  in  the stool  (MacGregor,
1954).  The toxicity appears  to  be  increased  if  taken dissolv-
ed in oil  (Solomon,  1957). The  oral  toxicity of a metabolite
of naphthalene, 1,4-naphtoquinone,  is  increased  at  least
fivefold when  administered, dissolved  in  oil, to rabbits
as compared to an aqueous  solution (Talakin,  1966). Sanborn
and Malins  (1977)  found a  marked decrease in  absorption
of naphthalene if bound to protein in shrimp.   The  authors
give this  as evidence  that naphthalene would  be  less likely
                               C-5

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           TABLE 1
  Air Levels of Naphthalene
      Area Investigated

      Industrial;
      Naphthalene  melt present
      Coke Oven

o     Aluminum Reduction Plant

      Ambient;
      Providence,  R.I.
      Kingston, R.I.
      Narragansett Bay, R.I.
    Air Level
Vapor
1600 -   ,
 1.1 x 10'
11.35 -
 1120
.72 -
 311.3
.0001
,00003
.00005
                                     Reference
                   articulate
                  0-4.40

                  .090-4.00
                  .00025
                  .00003
                  .000003
                                   Robbins, 1951
BjjzJrseth, et al. 1978a
Bj^rseth, et al. 1978b
Krstulovic, et al. 1977
Krstulovic, et al. 1977
Krstulovic, et al. 1977

-------
                      TABLE 2
    Workers with Potential Naphthalene Exposure
              (Tabershaw,  et  al.  1977)

Beta naphthol makers
Celluloid makers
Coal tar workers
Dye chemical makers
Fungicide makers
Hydronaphthalene makers
Lampblack makers
Moth repellant workers
Phthalic anhydride makers
Smokeless powder makers
Tannery workers
Textile chemical workers
Aluminum reduction plant  workers
                          C-7

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to be absorbed  when  exposure  was  from food than when from
water.
     When  dissolved  in  a nonpolar solvent, absorption of
naphthalene  by  skin  application caused less experimental
toxicity than when taken orally (Gaines, 1969). Dawson,
et al.  (1958),  however,  found that two infants exposed to
naphthalene  treated  clothes developed toxic effects after
their skin was  covered  with baby  oil.  These authors suggest
that  skin  absorption might be significant under these circum-
stances.
      Enough  absorption  can occur  by inhalation of  naphthalene
vapor to cause  significant toxicity.   Valaes,  et al.  (1963)
found toxicity  in  newborn infants when the only exposure
was to  naphthalene vapor from clothes or blankets  treated
with  naphthalene stored  in the infants'  rooms  or in an adja-
cent  hall. One  of  these  infants died.
     Naphthalene distributes  widely after absorption.  Lawler,
et al.  (1978) found  that in mallards  given naphthalene in
oil over a period  of  two weeks, naphthalene could  be  identi-
fied in all  tissues  examined.   Its relative distribution
was as follows: skin >liver7brain =  blood >muscle >heart.
Naphthalene  has not been  identified in urine after absorption.
With sufficient absorption  of  naphthalene to result in toxi-
city to an 18 month old  infant, Mackell,  et al.  (1951) noted
metabolites of naphthalene  in  the  urine  that were  still
identifiable two weeks after exposure  but which  had disappear-
ed 18 days after exposure.
                               C-8

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Metabolism
     The metabolism of naphthalene  has  been  extensively
studied in mammals<>  Naphthalene  is first  metabolized  by
hepatic mixed function oxidases to  the  epoxide,  naphthalene-
1,2-oxide  (Figure  1).  This  epoxide has the  distinction
of being the first arene  oxide metabolite  to have  been isolat-
ed (Jerina, et al. 1970).  Epoxide  formation is  an obligatory
step.  The epoxide can be enzymatically converted  into the
dihydrodiol, l,2-dihydroxy-l,2-dihydronaphthalene  or  conjugat-
ed with glutathione. The  dihydrodiol can then be conjugated
to form a  polar  compound  with glucuronic acid or sulfate
or be  further dehydrogenated to  form the highly  reactive
1,2-dihydroxynaphthalene. This  too can be enzymatically
conjugated to sulfate  or  glucuronic acid or  spontaneously
oxidized  to  form another  highly  reactive compound, 1,2-naphtho-
quinone.
     The  epoxide can  also be converted spontaneously to
1-naphthol or  2-naphthol  by  a keto tautomer intermediate
 (Boyd, et al.  1972).   1-naphthol is the predominant spontan-
eous decomposition product of the epoxide, being a more
stable resonant structure than 2-naphthol (Jerina, et al.
1970).  1-naphthol is excreted unchanged  as well as conjugat-
ed with glucuronic acid or sulfate prior  to excretion.
The  finding  of 1,4-naphthoquinone  in the  urine of a child
poisoned with naphthalene (Mackell, et  al.  1951) suggests
 that 1-naphthol can also be  further oxidized  in mammals
 (Cerniglia and Gibson, 1977).
                                C-9

-------
                                .S
                                       *•
                                         ;
Figure 1: Pathways for the Metabolism of Naphthalene
          (adapted from Bock, et al.  1976).
Enzymes: I- monooxygenase
        II- epoxide hydrase
       III- UDP-gluconyltransferase
        IV- glutathione-S-transferase
         V- dihydrodiol dehydrogenase
        VI- sulfotransferase
                              C-10

-------
     A number of other metabolites  have  been  found  in liver
cells, liver microsomal preparations  or  bile  as noted in
Table 3.  The glutathione conjugate can  be progressively
broken down to a cysteinylglycine compound and then a cys-
teine conjugate prior to acetylation  to  the mercapturic
acid, N acetyl-S-(l,2-dihydro-2-hydroxy-l-naphthyl)-L-cys-
teine either in the liver or  kidney (Booth, et al.  1960).
A number of these metabolites have  been  identified  in the
urine of mammals (Table 4). The  presence of 1-naphthyl mercap-
turic acid may be explained by a spontaneous  dehydrogenation
of the mercapturic acid of the dihydrodiol in acid  urine
(Jerina, et al. 1963).
     Naphthalene metabolites  undergo  further  conversions
in the eye.  The eye  contains beta  glucuronidase  and sulfa-
tase which can hydrolyze the  glucuronide and  sulfate esters
of the dihydrodiol  (Van Heyningen and Pirie,  1967). Catechol
reductase is also present in  the eye.  This enzyme  can oxi-
dize the dihydrodiol  to 1,2-dihydroxynaphthalene  which in
turn can be spontaneously oxidized  to 1,2-naphthaquinone
with the concomitant  release  of  hydrogen peroxide.  1,2-
naphthaquinoae can then oxidize  ascorbic acid, which is
found in hign concentration in the  eye,  to dihydroascorbic
acid with the release of more hydrogen peroxide.  Dihydroas-
corbic acid can then  be broken down to oxalate or diffuse
into the lens where it is reconverted to ascorbic acid with
the associated nonenzymatic oxidation of reduced  glutathione
(Van Heyningen, 1970). As 1,2-naphthaquinone  is reduced
by the reaction with  ascorbic acid  to l,2~dihydroxynaphtha-
lene, it oxidizes NADPH. The  dihydroxide will rapidly reduce
                               C-ll

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                                          TABLE 3
                            Naphthalene  Metabolites:   Liver/Bile
Metabolite
1-naphthol
2-naphthol
1-naphthyl glucosiduronic acid
1-naphthyl mercapturic acid
l,2-dihydro-l,2-dihydroxy napthalene
l,2-dihyro-2-hydroxy-l-naphthyl-
                glucosiduronic acid
l,2-dihydro-l-hydroxy-2-naphthyl-
                glucosiduronic acid
S-(l,2-dihydro-2-hydroxy-l-naphthyl)-L-
                cysteine
N-acetyl-S-(l,2-dihydro-2-hydroxy-l-naphthyl)
                1-cysteine
1,2-dihydroxy naphthalene
1,2-naphthoquinone
Naphthalene-l,2-oxide
S-(l,2-dihydro-2-hydroxy-l-naphthyl)-
                glutathione
S-(l,2-dihydro-2-hydroxy-l-naphthul)-
                L-cysteinyl glycine
(l,2-dihydro-2-hydroxy-l-naphthyl)-sulfate
2-hydroxy-l-naphthyl-glucosiduronic acid

Rabbit
2
2


2






Found in:
Rat
3,4
3
3,4
3
3,4
3,4
3
3
3
4
4

Fish
5

5
5
5
5





              2

              2
1,3

 3
 4
 3
References:    1-Booth, et al. 1960
4-Bock, et al. 1976

-------
                                                   TABLE .4
                                    Naphthalene Metabolites:  Kidney/Urine
O
i
H"
U>
Metabolite
1-naphthol
2-naphthol
1-naphthyl sulfate
1-naphthyl glucosiduronic acid
S-(1-naphthyl)-L-cysteine
1-naphthyl mercapturic acid
l,2-dihydro-l,2-dihydroxy naphthalene
l,2-dihydro-2-hydroxy-l-naphthyl-
                 glucosiduronic acid
l,2-dihydro-l-hydroxy-2-naphthyl-
                 glucosiduronic acid
S-(l,2-dihydro-2-hydroxy-l-naphthyl)-L-
                 cysteine
N-acetyl-S-(l,2-dihydro-2-hydroxy-
                 1-napthyl)-L-cysteine
2-hydroxy-l-naphthyl sulfate
l-hydroxy-2~naphthyl sulfate
1,2-dihydroxynapthalene
1,2-naphthoquinone
1,4-naphthoquinone
 Rabbit
 1,2
 1
 1,7
 1

 1
 1,5,7

 1/2,6,7

 2
                                                 1
                                                 1
                                                 2
                                                              Guinea Pig
                                                                    7
Found in:

      Mice
       7
       7
       7
Rat
7
7
7
                4,5,7

                7
                                        3

                                        1,3
Man
 9
 9
                                                                                                    9
                                                                                                    9
    References;
                1- Boyland & Sims, 1958
                2- Sims, 1959
                3- Booth, et al. 1960
4- Young, 1947
5- Booth & Boyland, 1949
6- Corner, et al. 1954
     7- Corner & Young,  1954
     8- Bourne & Young,  1934
     9- Mackell, et al.  1951

-------
cytochrome c  (Van Heyningen and Pirie, 1967). 1,2-naphthaqui-
none also binds irreversibly to lens protein and amino acids
(Van Heyningen and Pirie, 1966).
     Aryl hydrocarbon hydroxylasef a mixed-function microso-
roal oxidase,  is induced by many carcinogenic polycyclic
aromatic hydrocarbons.  Alexandrov and Frayssinet  (1973)
found that the intraperitoneal injection of 40 mg/kg of
naphthalene in corn oil into male Wistar rats daily for
a period of three days resulted in a 40 percent inhibition
of this enzyme's ability to hydroxylate benzo(a)pyrene.
Naphthalene also inhibited the inducability of this enzyme
by 3-methylcholanthrene.  A number of other napthtalene
derivatives,  including 1-naphthol and 2-naphthol,  were tested
and were not  found to depress the activity of this enzyme.

-------
                           EFFECTS



     Lezenius (1902) described the case of a 36-year-old



pharmacist who, after taking 5 g of naphthalene in oil,



developed near blindness eight or nine hours later.  An



examination a year  later disclosed constricted visual fields



associated with optic atrophy and bilateral cataracts made



up of numerous whitish opacities.  In 1906 Van der Hoeve



further described a case of a 44-year-man who worked with



powdered naphthalene and was found to have cataracts and a



retinal hemorrhage.  A coworker was noted to have  choriorctin-



itis in one eye.  Ghetti and Mariani  (1956) examined 21



workers in a plant  producing a dye intermediate  from naphtha-



lene and found cataracts in 8 of  them with the  following



age distribution:





                                    # with cataracts



                                          2



                                          3



                                          2



                                          1



     A model for  the  eye toxicity of  naphthalene has been



developed  in rabbits  (Van  Heyningen  and  Pirie,  1976) to



further investigate the disappearance of reduced glutathione



from the lens, first  noted by Bourne  (1937),  and its relation-



ship to the cataractogenicity of  naphthalene.   The authors



found that the metabolites of naphthalene released in  the



eye were general  metabolic and coenzyme  inhibitors (Rees



and Pirie, 1967);  that 1,2-dihydroxynaphthalene  or 1,2-naphtha-
                               C-15
Age
20-30
30-40
40-50
50-60
i
4
5
8
4

-------
quinone combined with amino  acids  or  irreversibly  with  the
thiol groups of lens protein to  form  a  brown  precipitate;
that the hydroperoxide  formed in the  oxidation  of  1,2-dihydro—
xynaphthalene and ascorbic acid  can act with  the high levels
of glutathione peroxidase in the eye  to oxidize glutathione;
that oxidized ascorbic  acid  easily enters  the lens where
it readily oxidizes reduced  glutathione nonenzymatically
(Van Heyningen, 1970);  that  the  oxidized ascorbic  acid  also
oxidizes protein thiols, a mechanism  that  is  normally prevent-
ed by reduced glutathione; that  the oxidation of NADPH  pre-
vents the reduction of  oxidized  glutathione by  glutathione
reductase; that 1,2-naphtoquinone quickly  combines irrevers-
ibly with lens and eye  proteins  thereby losing  its ability
to oxidize ascorbic acid (Van Heyningen and Pirie,  1967);
that oxidized ascorbic  acid  breaks down to oxalate which
in turn precipitates as calcium  oxalate crystals in the
vitreous humor and on the retina of the eye;  and that lens
changes are preceded by evidence of injury to the  epithelium
of the lens as well as  retina  (Pirie, 1968).
     A hemolytic anemia with associated jaundice and occasion
ally renal disease from precipitated hemoglobin has been
described both in children and adults (Haggerty, 1956; Chusid
and Fried,  1955;  Abelson and Henderson,  1951; Zuelzer and
Apt,  1949;  Gidron and Leurer, 1956; Nash,  1903; Mackell,
et al.  1951)  as well as in newborn infants (Cock,  1957;
Schafer, 1951)  after exposure to naphthalene  by ingestion,
inhalation or,  possibly, by  skin contact.  Dawson, et al.
(1958)  identified two newborn children who had both a naphtha
lene hemolytic anemia as well as a combined glucose-6-phosphate

                               C-16

-------
dehydrogenase deficiency and glutathione reductase deficiency.
The former defect was more prominent. Glucose-6-phosphate
dehydrogenase   (G6PD) in the presence of glucose-6-phosphate
reduces NAPD to NADPH which in  turn  is required by glutathione
reductase to maintain glutathione  in the reduced state.
In the absence of reduced glutathione there can be oxidative
denaturation of hemoglobin with precipitation of globin
as Heinz bodies and  the associated stiffening of red blood
cell membranes.  These abnormal red  cells  are then removed
from the circulation by the spleen and liver.  NADPH is
also a cofactor for  the reduction  of methemoglobin (Kellermeyer,
et al. 1962). This can lead to  the buildup of methemoglobin
or methemalbumin in  the serum with excretion of these compounds
in the urine  (Schafer, 1951). Both Valaes, et al.  (1963)
and Naiman and Kosoy  (1964) have noted that although most
infants with naphthalene-associated  acute  hemolytic anemia
have G6PD deficiency, there was a  group of neonates that
had a milder form of hemolysis  and did not have the enzyme
deficiency.  Both groups noted  high  levels of bilirubin
in the serum of their cases with associated brain damage
(kernicterus) and even death  in several infants.  Gross,
et al.(1958) noted that red blood  cells lose G6PD activity
with aging in G6PD deficient  individuals  such that older -
populations of red blood cells  are more susceptible to hemoly-
sis than young ones.  In some  forms  of G6PD deficiency,
this can result in a self-limited  form of  hemolysis  (Wintrobe,
et al. 1974).
                               C-17

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     Hemolytic anemia has also been noted in individuals
exposed to a metabolite of naphthalene, 2-naphthol. Smillie
(1920) treated 79 Brazilians with 2-naphthol for hookworm
disease. Adults received a 6 g a day orally for three days
while children received a smaller dose.  Four of those treated
were found to develop a hemolytic anemia, two associated
with splenomegaly.  He identified three of those affected
as being black.
Acute, Sub-acute, and Chronic Toxicity
     The acute lethality of naphthalene has been assessed
by several routes in several species as shown in Table 5.
The greater toxicity by an oral versus subcutaneous route
might be due to species variation in susceptibility but
might also indicate that naphthalene first has to be metabol-
ized by the liver to produce maximum toxicity.
     Several other studies have been performed to assess
sublethal effects of naphthalene or its metabolites. Zuelzer
and Apt (1949)  administered naphthalene in a solid form
to dogs by the oral route.  One dog received 1800 mg/kg
in divided doses over a period of five days with resultant
lethargy, ataxia, a drop in hemoglobin by 83 percent and
a leukamoid reaction (white blood cell count of 119,000).
Two other dogs received 1530 mg/kg and 420 mg/kg in single
doses with a resultant drop in hemoglobin by 33 percent
and 29 percent respectively.
                               C-18

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                                    TABLE  5

                   Tests of the Acute Toxicity of Naphthalene
Test Animal

Mice

Sherman rats

  male

  female


  male

  female

Rat

Rat

Rat
  Route
Subcut.
40

40

10

10
Oral0
a
Oral3
K
Skin0
K
Skin0
Oral

Oral

Inhalation
LD50 (mg/kg)   Reference

    5100       Irie, et al. 1973
    2200

    2400


   >2500

   >2500

    1780

    9430

  >100 ppm x
      8 hr.
Gaines, 1969

Gaines, 1969


Gaines, 1969

Gaines, 1969

NIOSH, 1977

Union Carbide Corp., 1968

Union Carbide Corp., 1968
  Dissolved in peanut oil

  Dissolved in xylene
                                    C-19

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     Mahvi, et al.(1977) administered naphthalene in corn
oil intraperitoneally to C57 B1/6J mice. Two groups of 63
mice received corn oil alone or remained untreated. Groups
of 21 mice each were given 67.4, 128, or 256 mg/kg. Three
animals from each dosage group were sacrificed at ten minutes,
1 hour, 6 hours, 12 hours, 24 hours, 48 hours, and 7 days
following treatment.  Lung tissue was rapidly fixed and
examined by light, scanning electron microscopy, and transmis-
sion electron microscopy.  No changes were noted in either
control group. Minor bronchiolar epithelial changes were
noted  in the group receiving 6.4 mg/kg. Mice  in the higher
dosage groups developed necrosis of  secretory nonciliated
bronchiolar cells.  Epithelial  structure  returned  to normal
within seven days in all cases.
     Reid,  et al.  (1973) gave  naphthalene dissolved  in  sesame
oil  to C57  B1/6J mice by the intraperitoneal  route and  found
coagulative necrosis of  the bronchiolar and  bronchial  epithel
 iura  at a dose of 600 mg/kg. Controls received sesame oil
 alone  and  no  adverse effects were reported for  this  group.
 The  size of the  treatment  groups was not stated.
      Pilotti,  et  al.  (1975)  treated ascites  sarcoma  BP8
 cells  in vitro  by  incubating with naphthalene solutions
 for  48 hours.   The  authors noted 100 percent growth  inhibition
 at a concentration  of  128  mg/1 and 10 percent growth inhibi-
 tion at a concentration of 12.8 mg/1.
                                C-20

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     Several studies have also been done on  the metabolites
of naphthalene.  Van Heyningen and Pirie  (1967) dosed one
rabbit with 300 mg of the dihydrodiol  intravenously  in divided
doses over three days and noted retinal lesions.  They also
noted lens changes in four rabbits dosed externally  with
one percent eye drops of the same compound  (dissolved in
water) over a period of two to five days for a total dose
of 40-70 mg per rabbit.
     Mackell, et al. (1951) incubated  blood  from normal
human donors with naphthalene or its metabolites in  various
concentrations.  Hemolysis was noted as shown in Table 6,
These agents were also injected intravenously into white
male rabbits in concentrations of 0.25, 0.5, 1.0 and 1.25
mg/kg.  Naphthalene, 2-naphthol,l,2-naphthaquinone and 1,4-
napthaquinone produced no hemolysis at 15 minutes after
the injection;  1-naphthol, however, produced six percent
and 9 percent hemolysis at the two higher dosages.   Zinkham
and Childs (1958) performed similar in vitro experiments
with the same metabolites but measured drop  in reduced gluta-
thione as an end point.  They also investigated the  effect
of these metabolites on blood from a patient who had hemoly-
sis after contact with naphthalene and who had red blood
cells sensitive to an oxidant (presumed G6PD) deficiency.
All four metabolites resulted in depression of reduced gluta-
thione levels. Naphthalene resulted in minor depression
of reduced glutathione levels at concentrations of 5000
mg/1 or greater.
                              C-21

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                                                TABLE 6


            In vitro Hemolysis of Red Blood Cells Exposed to Naphthalene and its Metabolites
            	                     (Mackell, et al. 1951)


                                                      Percent  Hemolysis

     Compound
     1-naphthol

     2-naphthol
i
g    1,4-naphtha-
       quinone

     1,2-naphtha-
       quinone

     Naphthalene
Concentration (mg/1 blood)
10
<2
0
0
0
0
13.3
6
0
0
0
0
2£
14
3
0
0
0
410
46
11
0
0
0
100
53
32
0
0
0
200
65
48
4
<1
0
1UUU
74
60
18
12
0

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     Several studies have been done on  the  subacute  and
chronic toxicity of naphthalene, all  involving  a  single
dose/day regime. Fitzhugh and Buschke  (1949)  fed  five wean-
ling rats two percent of naphthalene or 2-naphthol in their
diets for a period of at least 60 days  and  noted  early catar-
acts in both groups.
     Van Heyningen and Pirie  (1976) dosed rabbits daily
by gavage with 1000 mg/kg of naphthalene for  various periods
of time for a maximum of 28 days. They  noted  lens changes
developing after the first dose and retinal changes develop-
ing after the second dose.
     Ghetti and Mariani  (1956) fed five rabbits 1000 mg/kg/day
of naphthalene and noted the development of cataracts between
days 3 and 46.  Topical application of  a ten  percent solution
in oil to the eyes of two rabbits did not produce cataracts
after a period of 50 days.  Intraperitoneal injection of
500 mg/day of naphthalene in an oily solution to one rabbit
over a period of 50 days produced weight loss but no cataracts.
Synergism and Antagonism
     There is little information on the synergistic or antago-
nistic effects of naphthalene. In a single case report Harden
and Baetjer (1978) described finding aplastic anemia in
a 68-year-old black female exposed to mothproofing compounds.
Yearly for a period of 39 years she had intermittently worked
in storing garments with mothproofing compounds.  One month
prior to becoming ill she worked for a period of three weeks
in a hot, unventilated room mothproofing garments.  She
handled a total of 7 kg of naphthalene  and 5.5 kg of para-
                              023

-------
dichlorobenzene.   It  was estimated  that  she  was  exposed
to  at or near 1400 ppm  of paradichlorobenzene  and  184  ppm
of  napththalene..  The time of  her exposure was consistent
with the onset of  her bone marrow depression,  estimat-
ed  from her hematologic findings on admission  two  months
after first becoming  ill.  No  other cases of aplastic  anemia
have been described with either a naphthalene  or paradichloro-
benzene exposure either alone  or in combination  with another
chemical.
Teratogenicity
     Naphthalene or its metabolites can  cross  the  placenta
in  sufficient amounts to cause fetal toxicity.  Both Zinkham
and Childs  (1958)  and Anziulewicz,  et al.  (1959) noted toxic
effects in  infants where the only exposure was to  the  mother
during pregnancy.  When a metabolite of  naphthalene, 2-naph-
thol, was administered  to pregnant  rabbits,  their  offspring
were born with cataracts and evidence of retinal damage
(Van der Hoeve,  1913).
Mutagenicity
     Naphthalene has  been found to  be nonmutagenic in  several
microsomal/bacterial  assay  systems  as outlined in  Table 7.
Metabolites of naphthalene  have not been tested.
Carcinogenicity
     Wolf (1976)  reported six  cases of malignant tumors
among 15 workers exposed  to vapors  of naphthalene  and  coal
tar for a period of up  to 32 years  at a  coal tar naphthalene
production  facility.  Four workers  contracted  laryngeal
carcinoma and were all  smokers.  The other 2 workers devel-
oped neoplasms of  the pylorus  and cecum.  There  was  no con-

-------
                                                     TABLE 7


                    Mutagenicity of Naphthalene in Various  In Vitro Microsomal Assay  Systems
o
i
N>
en
      System


      Rat microsomes/

       Salmonella  typhimurium
Mouse microsome/
Salmonella typhimurium


Mouse microsome/

 E. coli
Strain


TA100


TA1535


TA1537


TA98




G46




K12
                                                                     Result
                                                               Negative'


                                                               Negative


                                                               Negative*


                                                               Negative*
                                                                     Neative
Negative
                                                                             a
Reference


McCann, et al. 1975


McCann, et al. 1975


McCann, et al. 1975


McCann, et al. 1975




Kraemer, et al. 1974




Kraemer, et al. 1974
      lLess  than  0.09  revertants/nmol.  Tested at 10,  100,  500 and 1000 ug/plate
       Naphthalene-l,2-oxide used in the test system

-------
trol group.
     Knake (1956) treated 40 white rats with 500 mg/kg of
coal tar naphthalene in sesame oil subcutaneously every
two weeks for a total of seven treatments; 34 rats survived
the treatment and five developed invasive or metastatic
lymphosarcoma prior to death.  There was a two percent inci-
dence of malignancies in an untreated control group with
a similar, incidence in a group treated with sesame oil alone.
His data are detailed in Table 8. The sites of the injections
of the naphthalene/sesame oil and sesame oil treated groups
were painted with carbolfuchsin  (a known experimental carcin-
ogen) prior to each injection.  The naphthalene contained
0.07 gram molecular weight  impurities per 100 g  (equivalent
to 10 percent methyl naphthalene).
     In a second study, Knake  (1956) painted a group of
mice with either benzene or a solution of coal tar naphtha-
lene in benzene  and noted an excess of lymphatic  leukemia
in the naphthalene/benzene  group compared to the  benzene
treated group or a group of untreated controls.   His  results
are detailed in  Table 9.
     Druckey and Schmahl  (1955)  used naphthalene  as a vehicle
for testing the  carcinogenic effects of  anthracene.   In
a preliminary study they looked  at  the potential  carcinogenic
effects of naphthalene alone.  BD  I  and  BD  III  strain rats
were used.  One  group of 28 rats was given  10 gm  of naphtha-
lene orally per  rat over a  period  of  time and  followed  for
an  excess  of 1000 days.  A  second  group  of  ten  rats was
 given  a total dose cf 0.82  gm  of naphthalene per  rat  subcu-
 taneously  and  followed  for  a similar period of  time.   No

                               C-26

-------
                                            TABLE 8

      Incidence of Tumors in White Rats Treated with 0.5 gm/kg Naphthalene Subcutaneously
       (15% in sesame oil) Every Two Weeks for 14 Weeks and  then Followed for  18 months
                                          (Knake, 1956)
Treatment
      Number or Animals

Total     Survivors     Lymphosarcoma
Fibroadenoma



n
i
N)
Naphthalene
in sesame oil
Sesame oil
No treatment


40
40
101


0
4
0 (lifetime)


5
1
1


1
1
0


0
0
1

Other Malignant Tumor
a34 naphthalene/sesame oil treated rats survived the initial treatment. 32 rats treated with
 sesame oil alone survived the initial 14 weeks of treatment

b-
 3.3 ml/kg/treatment

-------
                                                    TABLE 9


               Incidence of Tumors in Inbred Black Mice Painted with 0.5% Naphthalene  in  Benzene
                             or Benzene  Alone  5  days/week for Life  (Knake, 1956)
    Treatment          Number

    Naphthalene in
      Benzene             25
          Leukemia
          Lymphosarcoma


                1
Sarcoma       Other
(other)     Malignancy    Lung Adenoma


   013
    Benzene
  21
0
o   No Treatment
i
to
oo
1227
                                                                                  44
      All lymphocytic leukemia

-------
tumors were noted in either group.
     Boyland, et al. (1964) found a four percent incidence
of bladder carcinoma in mice with naphthalene implaced  in
their bladders.  As seen in Table 10, there was a similar
or higher incidence of bladder carcinoma in mice treated
with various inert control substances including glass,
     Kennaway  (1930) and Kennaway and Hieger  (1930) tested
the carcinogenicity of naphthalene in mice by a skin painting
experiment.  They found that naphthalene was noncarcinogenic,
but did not give the details of their protocols.
     Bogdat'eva and Bid (1955) painted naphthalene onto
the skin of rabbits at a dose sufficient to cause systemic
toxicity.  No carcinomatous changes were noted after this
chronic study.  Details of the protocol were not given.
     Takizawa  (1940) painted the skin of mice with a metabo-
lite of naphthalene, 1,4-naphthaquinone.  They noted an
incidence of 15 to 20 percent skin papillomas with some
degenerating into malignant epithelomas in mice surviving
200 days. Further details of the protocol were not given.
     Pirie  (1968) treated Dutch and albino rabbits with
lg/kg/day of naphthalene by gavage. After three doses  they
noted mitotic arrest of the epithelial cells of the lens.
The arrest persisted for 15 days when replication of the
epithelial cells was first noted*  At 16 days numerous  abnor-
mal mitotic  figures  in metaphase were noted  in the epithelial
layer in association with cell overgrowth. This work is
significant  in  that  one of the effects of 2 metabolites of
naphthalene, 1-naphthol and 2-naphthol, is to interfere
with  the mitotic spindle function, as seen in root tips
                               C-29

-------
                                                  TABLE 10

                          Bladder Tumors  in Mice with Naphthalene Bladder  Implants
                                            (Boyland, et al.  1964)
o
i
Substance
Naphthalene
Inert Controls
  Magnesium stearate
  n-Hexadecanol
  n-Octadecanol
  Smooth glass
  Roughened glass
                                      # Mice Surviving
                                         to 30 weeks
Carcinoma
Adenoma/Papilloma
23
41
69
50
67
63
1
1
6
6
3
18
0
1
2
7
	
	

-------
of Vicia faba (Dean, 1978).  Both metabolites cause a chromo-



somal lagging in anaphase and 1-naphthol results in a colchi-



cine-like accumulation of chromosomes in metaphase.



     Naphthalene has also  been tested for carcinogenic



activity in in vitro test systems using rodent embryo cells



pretreated with Rauscher leukemia virus.  No effects were



seen at doses up to 100,000 pg/1  (Table 11).
                               C-31

-------
                                                 TABLE 11
                     Carcinogenic Activity of Naphthalene with  In Vitro Test  Systems
o
i
u>
N)
     Test System
     Rat embryo cells/

      Rauscher leukemia virus
          Dose (ug/1)-
Result
Reference
a
     Mouse embryo cells/.

      AKR leukemia virus*

1
5
10
50
100


1
5
50
,000
,000
,000
,000
,000
100
500
,000
,000
Negative
Negative
Negative
Negative
Negative
Negative
Negative
Negative
Negative
Negative
Freeman,
Freeman,
Freeman,
Freeman,
Freeman,
Freeman,
Rhim, et
Rhim, et
Rhim, et
Rhim, et
et
et
et
et
et
et
al.
al.
al.
al.
al. 1973
al. 1973
al. 1973
al. 1973
al. 1973
al. 1973
1974
1974
1974
1974
     a In addition  to  transforming  ability,  treated  cells  injected  into newborn rats or  mice,

       respectively, without  any  evidence  of  tumorigenicity
       Dissolved  in  acetone

-------
                     CRITERIA_FQRMULATION
Existing Guidelines and Standards
     The only existing U.S. standard  for  naphthalene  is
the Occupational Safety and Health Administration  standard
of 10 ppm  (50 mcf/nT) of vapor exposure  for  a  time-weighted
industrial exposure  (39FR23540).  This  standard  was adopted
from the American Conference of Governmental  Industrial
Hygienists1 Threshold Limit Value which in  turn  was based
on an irritant threshold  for naphthalene  of 15 ppm (ACGIH,
1971). At present the ACGIH also suggests a maximum 15 minute
exposure value of 15 ppm  (75 mg/m3)(ACGIH,  1978).
     The maximum permissible concentration  of naphthalene
in fishery water bodies of  the  USSR  is  4  ;ig/l (Mosevich,
et al. 1976).
Current Levels of Exposure
     Natural waters  have  been found  to  contain up  to  2 /ig/1
of naphthalene while drinking water  supplies  have  been  found
to contain up to 1.4 /ag/1 of naphthalene  (U.S.EPA, Region
IV,  unpublished data)»  Ambient air  levels  have  been  measured
at .00035 jug/m3 in  an urban area and  .00006 /ag/nr'  in  a  small
town  (Krstulovic, et al.  1977).  Industrial exposures can
range as high as 1.1 x  10 ;ig/m for  naphthalene-using  indust-
ries  (Robbins, 1951) with exposures  up to 1120 /ig/m   for
coke oven  workers  (Bjorseth, et al.  1978a)  and  310 /ag/m
for  aluminum reduction  plant workers (Bjorseth,  et al.  1978b)
No measurements of  naphthalene  have  been reported  for market
basket  foods.
                               C-33

-------
 Special Groups at Risk
     Approximately 100 million people worldwide have G6PD
deficiency which would make them more susceptible to hemoly-
tic anemia on exposure to naphthalene. At present more than
80 variants of this enzyme deficiency have been identified
(Wintrobe, et al. 1974). The incidence of this deficiency
is 0.1 percent in American and European Caucasians but can
range as high as 20 percent in American blacks and greater
than 50 percent in certain Jewish groups  (Table 12) .
     Newborn infants have a similar sensitivity to the hemoly-
tic effects of naphthalene, even without G6PD deficiency.
Zinkham and Childs  (1957) surveyed 26 normal white and black
newborn infants and found that their  blood reduced gluta-
thione levels dropped moderately to severely in all of the
samples tested when incubated with acetylphenylhydrazine,
suggestive of a glutathione reductase deficiency.  Brown
and Burnett  (1957)  also noted that newborn  infants have
a decreased capacity  to conjugate chemical metabolites with
glucuronide secondary  to an absolute  decrease  in  the  activity
of UDP-glucuronyl dehydrogenase  and  transferase.   Such a
lack in glucuronidation can allow the build-up of toxic
amounts of 1,2-dihydroxynaphthalene  and 1,2-naphthaquinone.
     A small percentage of the population might have  an
allergic  hypersensitivity to  naphthalene. Fanburg (1940)
described a 43-year-old physician with  a generalized  exfolia-
 tive dermatitis  who was found to be  allergic to naphthalene.
 Both the  clinical and histologic picture resembled a  malig-
 nancy,  mycosis fungoides. A  patch  test with naphthalene

                               C-34

-------
                         TABLE 12
       Frequency of G6PD Deficiency  in Populations
                  (Wintrobe, et al. 1974)
Population                          G6PD Deficiency  (%)
Northern European                            0.1
American black male                         13
American black female                       20
Brazilian black male                         8.2
Bantu male                                  37
Sardinian                                   14.35
Maltese                                      2.7
Italian                                      0.4
Greek                                        9.5
Sephardic, Oriental or Kurdish Jews
                        C-35

-------
was positive, resulting  in urticaria.  When all exposute
to naphthalene was discontinued, the skin condition cleared
rapidly and did not  recur over a three year period of  followup.
Basis and Derivation of  Criterion
     All chronic  toxicity studies using naphthalene have
failed to demonstrate any carcinogenic activity except  for
those performed by Knake (1956). This author  found an  excess
occurrence of lymphosarcoma when naphthalene  was given  by
the subcutaneous  route to rats, and of lymphocytic leukemia
when naphthalene  was chronically painted on the skin of
mice using benzene as a  solvent.  However, the naphthalene
used in this study was derived from coal tar  and contained
ten percent or more  unidentified impurities.  Furthermore,
a known experimental carcinogen, carbolfuchsin, was applied
prior to each injection  of naphthalene in the former study.
In light of these defects, carcinogenicity data derived
from this study cannot be used as a basis for a naphthalene
water criterion.
     No other chronic toxicity studies are available that
can be used as an adequate basis for a naphthalene criterion.
Furthermore, there are no adequate epidemiologic studies
that can be used  as  a basis.
     The ACGIH (1971) has recommended a time-weighted  thres-
hold limit value  for an  industrially exposed  population
of 50 mg/m  (50 ug/1) of naphthalene vapor in air. This
value was set to  prevent workers with exposure to naphthalene
vapors from getting  eye  irritation.  It is unclear, however,
whether exposures to water containing naphthalene in excess
of this level (50 ug/1)  might also result in  mucous membrane
                               C-36

-------
irritation.  Until further information  is available on the
direct irritant properties of naphthalene in water, the
ACGIH threshold limit value cannot be used as a basis for
a naphthalene water criterion.
     Mahvi, et al. (1977) noted a dose  related response
by C57 B1/6J mice given  intraperitoneal injections of naphtha-
lene in sesame oil.  No  bronchiolar  epithelial changes were
noted in two control groups.  The authors noted minimal
bronchiolar epithelial changes  in the  treated group receiving
6.4 mg/kg of naphthalene. Severe, reversible damage to bron-
chiolar epithelial cells was  noted  among two higher dosage
groups.  The results of  this  study  can be used as the basis
for the criterion.  The  minimal effect level of  6.4 mg/kg
is equivalent to  a 448 mg dose  for  a 70 kg  man and can  reason-
ably be used as a basis  for  calculating an  acceptable daily
dosage if  it is reduced  by  a factor of 1000, which equals
448 ug, to protect sensitive individuals (Natl.  Acad. Sci.,
1977) .
     No pharraacokinetic  data are available  on  the absorption
of naphthalene by the  oral  route.  Because of its high octanol:
water  partition coefficient (Krishnamurthy and Wasik,  1978),
it is  reasonable  to  expect  that naphthalene in water should
be nearly  completely absorbed and an absorption efficiency
of 100 percent can  be  assumed.
      For  the  purposes  of establishing  a water quality criter-
ion,  human exposure  to napthalene is considered to be based on
ingestion  of  2  liters  of water and 18.7 g of fish.  Fish
bioaccurnulate  naphthalene from water by a factor of 60.
                                C-37

-------
     With these considerations in mind, the following equa-
tion can be used to calculate a criterion value:
          2 L * X + (0.0187 X 60) * X = 448 ug
     Where:
          448 ug = limit on daily exposure for a 70 kg person
                   (ADI)
          2 L = amount of drinking water consumed
          0.0187 kg = amount of fish consumed
          60 = bioaccumulation factor
     Solving for X:
          X = 143 ug/1
     Thus, the recommended ambient water quality criterion
is 143 ug/1.
     This calculation assumes that 100 percent of man's
exposure is assigned to the ambient water pathway.  Although
it is desirable to arrive at a criterion level for water
based on contribution to total exposure, data on other routes
of exposure is not sufficient to support a factoring of
the criterion level.
     In summary, based on the use of toxicologic data for
mice, the criterion level corresponding to an acceptable
daily intake of 448 ug/day, is 143 mg/1.  Drinking water
contributes 64 percent of the assumed  exposure while eating
contaminated fish products accounts for 36 percent.  The
criterion can alternatively be expressed as 400 ug/1 if
exposure is assumed to be from the consumption of fish and
shellfish alone.
                               C-38

-------
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