Testing Status of Dicyclohexylcarbodiimide M930062
CASRN: 538-75-0
Formula: C13-H22-N2
Synonyms/Common Names
- Bis(cyclohexyl)carbodiimide
- DCC
Short-Term Toxicity
- 2 weeks (Topical Application)
(C93021)
Completed
- Rats: F344/N; Mice: B6C3F1
- Dose: R&M: 0, 2, 6, 17, 50, OR 150 MG/ML; 5/SEX/SPECIES/GROUP.
- 13 weeks (Topical Application)
(C93021)
Completed
- GMM-09 (NIH Number: 07-4426)
(Peer Review Approval 08/28/2006A )
Toxicology Studies of Dicyclohexylcarbodiimide (CASRN 538-75-0) in F344/N Rats, B6C3F1 Mice, and Genetically Modified (FVB Tg.AC Hemizygous) Mice and Carcinogenicity Study of Dicyclohexylcarbodiimide in Genetically Modified [B6.129-Trp53tm1Brd (N5) Haploinsufficient] Mice (Dermal Studies) - Rats: F344/N; Mice: B6C3F1
- Dose: R: 0, 0.75, 1.5, 3, 6, OR 12 MG/KG M: 0, 1.5, 3, 6, 12, OR 24 MG/KG; 10/SEX/SPECIES/GROUP; 6 GROUPS.
- GMM-09 (NIH Number: 07-4426)
(Peer Review Approval 08/28/2006A )
- 20 weeks (Topical Application)
(C93021B)
Completed
- GMM-09 (NIH Number: 07-4426)
(Peer Review Approval 08/28/2006A )
Toxicology Studies of Dicyclohexylcarbodiimide (CASRN 538-75-0) in F344/N Rats, B6C3F1 Mice, and Genetically Modified (FVB Tg.AC Hemizygous) Mice and Carcinogenicity Study of Dicyclohexylcarbodiimide in Genetically Modified [B6.129-Trp53tm1Brd (N5) Haploinsufficient] Mice (Dermal Studies) - Mice: Tg.AC (FVB/N) Hemizygous
- Dose: FEMALE MICE: 0, 0.75, 1.5, 3, 6, 12 MG/KG; 10/GROUP.
- GMM-09 (NIH Number: 07-4426)
(Peer Review Approval 08/28/2006A )
- 27 weeks (Topical Application)
(C93021C)
Completed
- GMM-09 (NIH Number: 07-4426)
(Peer Review Approval 08/28/2006A )
Toxicology Studies of Dicyclohexylcarbodiimide (CASRN 538-75-0) in F344/N Rats, B6C3F1 Mice, and Genetically Modified (FVB Tg.AC Hemizygous) Mice and Carcinogenicity Study of Dicyclohexylcarbodiimide in Genetically Modified [B6.129-Trp53tm1Brd (N5) Haploinsufficient] Mice (Dermal Studies) - Mice: P53 +/- (C57BL/6)
- Carcinogenesis Results
- Female No Evidence
- Dose: 0, 0.75, 1.5, 3, 6, OR 12 MG/KG; 15/GROUP.
- GMM-09 (NIH Number: 07-4426)
(Peer Review Approval 08/28/2006A )
Special Studies
- Absorption Distribution Metabolism Excretion (Intravenous; Topical Application; Intravenous; Topical Application)
(S0663)
Completed
- Male Rats: F344/N; Male Mice: B6C3F1
- Dose: 0.3, 3 mg/kg, indwelling jugular cannula. 0.3, 3 mg/kg, protective appliance used. 0.4, 0.6 mg/kg, lateral tail vein. 0.7, 6.2 mg/kg.
Genetic Toxicology
- Micronucleus
(A45449)
Completed
- Citation: Witt, K.L., Tice, R.R., Shelby, M.D., Chhabra, R.S., and Zeiger, E. Induction of Micronucleated Erythrocytes in Rodents by Diisopropylcarbodiimide and Dicyclohexylcarbodiimide: Dependence on Exposure Protocol. Environ. Molec. Mutag. Vol. 33 (1999) 65-74
- Rats: Fischer 344
- Male Negative
- Micronucleus
(A63966)
Completed
- Citation: Witt, K.L., Tice, R.R., Shelby, M.D., Chhabra, R.S., and Zeiger, E. Induction of Micronucleated Erythrocytes in Rodents by Diisopropylcarbodiimide and Dicyclohexylcarbodiimide: Dependence on Exposure Protocol. Environ. Molec. Mutag. Vol. 33 (1999) 65-74
- Mice: B6C3F1
- Male Weakly Positive
- Female Weakly Positive
- Salmonella
(A46724)
Completed
- Negative
Organ Systems Toxicity
- 4 days, 6 days, 8 days Immunotoxicity (Topical Application)
(IMM96015)
Completed
- Female Mice: B6C3F1
- Dose: 0, .003, .006, .03, & .06% IN ACETONE (99.8%) FOR SENSITIZATION, & .1% FOR CHALLENGE IN THE MEST & .006, .03, .06, AND .1% FOR SENSITIZATION IN THE LLNA. 25% DNFB WAS USED AS THE POSITIVE CONTROL FOR SENSITIZATION, & .5% FOR CHALLENGE.