Symmetrical dimethylhydrazine
Names | |
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IUPAC name
1,2-Dimethylhydrazine[2]
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Other names | |
Identifiers | |
3D model (JSmol)
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Abbreviations | SDMH[1] |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.149.162 |
KEGG | |
MeSH | 1,2-Dimethylhydrazine |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties[3] | |
C2H8N2 | |
Molar mass | 60.100 g·mol−1 |
Appearance | Colourless liquid |
Odor | Ichtyal, ammoniacal |
Density | 827.4 kg m−3 (at 20 °C) |
Melting point | −9 °C (16 °F; 264 K) |
Boiling point | 87 °C; 188 °F; 360 K |
Miscible | |
Thermochemistry | |
Heat capacity (C)
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171.04 J K−1 mol−1 |
Std molar
entropy (S⦵298) |
199.15 J K−1 mol−1 |
Std enthalpy of
combustion (ΔcH⦵298) |
−1.9872–−1.9788 kJ mol−1 |
Related compounds | |
Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1,2-Dimethylhydrazine, or symmetrical dimethylhydrazine, is one of the two isomers of dimethylhydrazine. It is a potent carcinogen that acts as a DNA methylating agent. It is used to induce colon tumors in experimental animals.[2][4][5]
See also
References
- ^ a b c d 74-79-3 1,2-Dimethylhydrazine
- ^ a b 1,2-Dimethylhydrazine from PubChem
- ^ Record of 1,2-Dimethylhydrazin in the GESTIS Substance Database of the Institute for Occupational Safety and Health, accessed on 21 March 2008.
- ^ Cruse, J. P.; Lewin, M. R.; Ferulano, G. P.; Clark, C. G. (1978). "Co-carcinogenic effects of dietary cholesterol in experimental colon cancer". Nature. 276 (5690): 822–5. doi:10.1038/276822a0. PMID 723955.
- ^ Wijnands, M.V.W. (1999). "A comparison of the effects of dietary cellulose and fermentable galacto-oligosaccharide, in a rat model of colorectal carcinogenesis: fermentable fibre confers greater protection than non-fermentable fibre in both high and low fat backgrounds". Carcinogenesis. 20 (4): 651–6. doi:10.1093/carcin/20.4.651. PMID 10223195.