Unttrt Stttw OHio* of Pwidd* and Toxic Sub««ne« EnvironiMnttl Protection Offlot of PMiold* Programs (T8-766C) AgMiey Wuhlngton, DC 20460 vvEPA Pesticide Fact Sheet Name of Chemical: Reason for Issuance: Date Issued: I4arch 3' 1985 Fact Sheet Number: 47 1. Description of chemical Generic Name: Substituted Dimethyl Hydantoin Common name: 1,3-Bis(Hydroxymethyl)-5,5-dimethylhydantoin Trade name: Glycoserve EPA Shaughnessy code: 115501 Chemical abstracts service (CAS) number: 273AB Year of initial registration: 1985 Pesticide type: Disinfectant Chemical family (e.g., carbamates) Hydantoins U.S. and Foreign producers: Glyco 2. use patterns and formulations Application sites: End-use products as a preservative in paints, room deodorizers, and dishwashing detergents as a Manufacturing Use Pesticide for reformulating use as a preservative in paints, room deodorizers and detergents. Types of formulations: Liquids Types of Methods of application: manual Application rates: 0.2% to 1% in paints, 0.25 to 1% in room deodorizer and detergents. Usual carriers: water 3. Science Findings Summary science statement: No mutagenic, or oncogenic effects are anticipated at the use dilutions recommended for the proposed uses. Chemical Characteristics: physical state-liquid, color-water white, odor-slight formaldehyde odor, boiling point-101.2°C Unusual handling characteristics: Protect eyes and skin when handling. Toxicology characteristics: Toxicology Category and value for each acute hazard. Testing Laboratory Warf institute Acute oral LD5Qf Toxicity Category III * LD50 = 2.00 to 3.65 g/kg (M) 3.00 to 5.00 g/kg (F) no signs of toxicity ------- Testing Laboratory: IBT 3.72 mg/kg hypoactivity, lacrimation, weakness, labored respiration. b. Testing Laboratory: Warf Institute *Acute inhalation toxicity category IV LC 50 >204 mg/L/hr gasping c. Testing Laboratory: Food and Drug Research Lab. LC 50 >377.8 ug/L/4 hrs slight irritation of mucous membranes envanol nose and eyes d. Testing Laboratory: Bio/dynamics *primary eye irritation Toxicity Category IV Negative using 0.1 ml of 0.1% solution e. Testing Laboratory: Warf Institute *Acute Derrnal LD 50 = >20 gm/kg f. Testing Laboratory: Warf Institute *Acute dermal irritation PIS = 1.5 ** Acute oral LD 50 — rat; LD 50 = 2.0 to 3.65 g/kg(male) Warf Institute; #6051229 LD 50 = 3.0 to 5. g/kg(female) 9/30/76 (highest dose tested log/kg) ** Acute oral LD 50 — rat; LD 50 = 3.720 g/kg IBT; *853009420; 9/22/76 (highest dose tested 15,380 g/kg) Key * Test conducted using 1,3—hydroxymethyl)—5,5-dimethyl hydrontoin 44% and hydroxymethyl—5,5 dimethyl hydantoin ** = Test conducted using the product as formulated glyco Major routes of exposure in order of toxicological significance. ------- ** Dermal patch test — human; IBT; #8537—09670; 12/3/76 ** Dermal absorption — rat; EG & G Mason Research Institute; Report MRI— 206—GC—83—35; 9/9/83 ** Patch test— human; Food and Drug Research Lab,; #18;l0/11/8 1 ** Acute oral LD 50 — rat; Wart Institute; #6051229; 9/30/7 6 ** Mutagenic; unscheduled DNA synthesis; Lab not stated; no. M0017;5/7/82 ** Mutagenic— Ames; Litton Bionetics; * 20838; 3/78 ** Mutagenic— Ames; Micro- biological Associates T 1804.502; 9/3/82 ** Mutagenic— Ames; Micro- biological Associates; T 1804.502; 9/3/82 ** Mutagenic— chinese ham- ster ovary in Vitro ; Microbiological Assoc •; #003—560—723—2; 2/23/82 ** Mutagenic— induction in mammalian cells— mice; Microbiological Assoc.; #003—561—724—7; 4/30/82 IBT — invalid Dynamac Corp. 2/25/83 Body burden <1% < than 3% was absorbed and the main portion was recovered in the urine. (Note 0.1 ml = 3.15 mg) Addendum Maximum absorption in 10 hrs. 10.01528 ml = 0.4813 mg 1/2 hr. (minimal absorption) 0.02406 mg 10 repeated insult path test in 31 males and 171 temales with 0.21 ml of test material produced negative results for sensitization LD 50 = 2.00 to 3.65 g/kg (M) 3.00 to 5.00 g/kg (F) (no signs of toxicity) Positive induced a dose—related increase in the number of grains per nucleus Negative with and without activa- tion Positive for TA 100 and TA 98 with and without metabolic activation Negative for TA 1535, TA 1538 and TA 98 Positive; significant increase in chromosomal aberrations with and without S—9 activation Positive with and without activa— t ion Key * Test conducted using l,3—hydroxymethyl)—5,5—dimethyl hydrontoin 44% and hydroxymethyl—5,5 dimethyl hydantoin ** = Test conducted using the product as formulated glyco 3 ------- ** Mutagenic— DNA synthesis Positive for induction of unsched— —rat; Microbiological uled DNA synthesis Assoc.; #M0017; 5/7/82; Report * 25 Note: Contains up to 2% Free Formaldehyde Chronic toxicology results, include size of data base; conclusions in each major toxicology area: Metabolism — rat; EG & E 97% recovered from treatment site Mason Research Institute; 2% recovered in urine @206—GC—35; 9/9/83 1% recovered in tissue and feces (body burden less than 1%) * Mutagenic Ames Negative with and without activation salmonella; Litton Bionetics; #20838; 3/78 * 90 Day oral — rat; NOEL > 400 mg/kg (HDT). Levels Food and Drug Research tested by gavage in Sprague— Lab.; #7059; 3/16/82 Dawley strain — 0,100, 200 and 400 mg/kg/day for weeks 1—8, than 0, 100, 300 and 600 mg/kg/day for weeks 9—13. * Mutagenic Ames Positive on tester strains TA100 and salmonella mammalian TA98 with or without metabolic microsome; Microbio— activation logical Assoc; *T1804— 502; 9/3/81 * Mutagenic Ames Negative with without metabolic salmonella mammalian activation microsome; Microbio- logical ASSOc; #003— 520—723—1; 2/23/82 * Mutagenic cytogenicity — Positive with or without metabolic CR0 cell in vitro; activation. Produced chromosomal Microbiological Assoc; aberrations #T1721.337; 5/25/82 Key * Test conducted using 1,3—hydroxymethyl)—5,5—dimethyl hydrontoin 44% and hydroxymethyl—5,5 dimethyl hydantoin ** = Test conducted using the product as formulated glyco ------- Physiological and Biochemical Behavioral Characteristics: Foliar absorption (if applicable). N/A Translocation (if applicable) N/A Mechanism of pesticidal action. Hydrolysis in water to yield free formaldehyde (which is the disinfecting agent) Metabolism and persistence in plants and animals. N/A Environmental Characteristics: (for indoor use only) Adsorption and leaching in basic soil types. N/A Microbial breakdown. N/A Loss from photodecomposition and/or volatization. N/A Bioaccumulation N/A Resultant average persistence. N/A Ecological Characteristics: As proposed, the product provides for minimal hazard to non—target organisms and due to the low toxicity of the product no F & W precautionary toxicity statements are required. Tolerance assessments: N/A. Registered use is not for use on food or feed stuffs. problems which are known to have occurred with the use of the chemical (e.g., PIMS data). None 4. Summary of Regulatory Position and Rationale : Use, formulation, manufacturing process or geographical restrictions (including classification for restricted use). No restrictions Unique warning statements required on labels (e.g., protective clothing requirements, restrictions regarding use around water, reentry intervals). None Summary of risk/benefit review in cases where risk assessments were conducted. Benefits exceed risks for use of the product as a preservative in paints, room deodorizers and soft detergents. 5. Summary of major data gaps There are no data gaps for the approved uses. ------- 6. Contact person at EPA: A. E. Castillo (PM 32) Disinfectants Branch Registration Division (TS—767C) Environmental Protection Agency 401 M St., SW. Washington, DC 20460 Phone: (703) 557—3964 DISCLAIMER: The information presented in this Chemical Information Fact Sheet is for informational purposes only and may not be used to fulfill the data requirements for pesticide registration and reregistration. ( .0 ------- |