| Identification | |
| Name: | Benzenamine,N-nitroso-N-phenyl- |
| Synonyms: | Diphenylamine,N-nitroso- (7CI,8CI);Diphenylnitrosamine;N,N-Diphenyl-N-nitrosoamine;N,N-Diphenylnitrosamine;N-Nitroso-N-diphenylamine;NSC 585;Nitrosodiphenylamine;Ortard;Redax;Retarder J;Sconoc;Vulcatard A;VulkalentA;Vultrol; |
| CAS: | 86-30-6 |
| EINECS: | 201-663-0 |
| Molecular Formula: | C12H10N2O |
| Molecular Weight: | 198.22 |
| InChI: | InChI=1/C12H10N2O/c15-13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H |
| Molecular Structure: |  |
| Properties | |
| Transport: | UN 1230 3/PG 2 |
| Density: | 1.23 |
| Stability: | Stability Combustible. Incompatible with oxidising agents. |
| Water Solubility: | Insoluble |
| Solubility: | Insoluble |
| Appearance: | orange to brown solid |
| Specification: |
Diphenylnitrosamine (86-30-6) is orange to brown solid, soluble in Acetone , Benzene , Ethyl acetate , Dichloromethane , Carbon tetrachloride , Carbon disulfide , hot Alcohol , slightly soluble in Gasoline , insoluble in Water . It is also called for Vultrol ; Redax ; Vulcatard A ; Retarder J ; Ortard ; Sconoc ; Vulcalent A ; Vulkalent A ; N-Nitrosodiphenylamine ; Diphenylnitrosoamine ; N-Nitroso-N-phenylaniline . Diphenylnitrosamine (86-30-6) can be used as anti-coke agent for natural rubber, synthetic rubber except butyl rubber in industry, also be used as re-plasticizer for a slight scorch plastic material, efficient anion polymerization inhibitor for chloroprene rubber instead of Creosote , intermediate for antioxidant 4010 and dye. |
| Report: |
IARC Cancer Review: Group 3 IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 7 , 1987,p. 56.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) ; Animal Limited Evidence IMEMDT IARC Monographs on the Evaluation of Carcinogenic Risk of Chemicals to Man . 27 , 1982,p. 213.(World Health Organization, Internation Agency for Research on Cancer,Lyon, France.: ) (Single copies can be ordered from WHO Publications Centre U.S.A., 49 Sheridan Avenue, Albany, NY 12210) . NCI Carcinogenesis Bioassay (feed); Clear Evidence: rat NCITR* National Cancer Institute Carcinogenesis Technical Report Series. (Bethesda, MD 20014) No. NCI-CG-TR-164 ,1979. ; No Evidence: mouse NCITR* National Cancer Institute Carcinogenesis Technical Report Series. (Bethesda, MD 20014) No. NCI-CG-TR-164 ,1979. . Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program. Community Right-To-Know List. |
| Storage Temperature: | 2-8°C |
| Color: | Yellow plates from petroleum ether |
| Usage: | An effective radical scavenger, and can be used to stabilize monomers, polymers, and petroleum products. In rubber processing, its major use is believed to be as an anti-scorching agent, or vulcanization retarder, during rubber compounding. |
| Safety Data | |
| Hazard Symbols |
Xn: Harmful
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