Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H8N2O |
| Molecular Weight | 88.1084 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(C)N=O
InChI
InChIKey=RTDCJKARQCRONF-UHFFFAOYSA-N
InChI=1S/C3H8N2O/c1-3-5(2)4-6/h3H2,1-2H3
| Molecular Formula | C3H8N2O |
| Molecular Weight | 88.1084 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Molecular modeling of nitrosamines adsorbed on H-ZSM-5 zeolite: an ONIOM study. | 2008-11 |
|
| N-nitrosodimethylamine (NDMA) formation during ozonation of dimethylamine-containing waters. | 2008-02 |
|
| Kinetics and mechanisms of the reactions of hydroxyl radicals and hydrated electrons with nitrosamines and nitramines in water. | 2006-04-13 |
|
| DNA repair capacity in lymphocytes of nasopharyngeal cancer patients. | 2005-07 |
|
| Role of human cytochrome P450 (CYP) in the metabolic activation of N-alkylnitrosamines: application of genetically engineered Salmonella typhimurium YG7108 expressing each form of CYP together with human NADPH-cytochrome P450 reductase. | 2001-11-01 |
|
| Carcinogenesis by nitrosodialkylamines and azoxyalkanes given by gavage to rats and hamsters. | 1987-08-01 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:45:03 GMT 2025
by
admin
on
Mon Mar 31 18:45:03 GMT 2025
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| Record UNII |
00RLM29Y3A
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| Record Status |
Validated (UNII)
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10595-95-6
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