Symmetrical dimethylhydrazine
| |
| |
| Names | |
|---|---|
| Preferred IUPAC name
1,2-Dimethylhydrazine[2] | |
| Other names | |
| Identifiers | |
3D model (JSmol)
|
|
| Abbreviations | SDMH[1] |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.149.162 |
| KEGG | |
| MeSH | 1,2-Dimethylhydrazine |
PubChem CID
|
|
| RTECS number |
|
| UNII | |
| UN number | 2382 |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties[3] | |
| C2H8N2 | |
| Molar mass | 60.100 g·mol−1 |
| Appearance | Colourless liquid |
| Odor | Fishy, 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)
|
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) |
−1987–−1978 kJ mol−1 |
| Hazards | |
| GHS labelling:[4] | |
  
| |
| Danger | |
| H301, H311, H331, H350, H411 | |
| P201, P202, P261, P264, P270, P271, P273, P280, P281, P301+P310, P302+P352, P304+P340, P308+P313, P311, P312, P322, P330, P361, P363, P391, P403+P233, P405 | |
| Related compounds | |
Related compounds
|
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Symmetrical dimethylhydrazine (SDMH), or 1,2-dimethylhydrazine, is the organic compound with the formula (CH3NH)2. It is one of the two isomers of dimethylhydrazine. Both isomers are colorless liquids at room temperature, with properties similar to those of methylamines. Symmetrical dimethylhydrazine is a potent carcinogen that acts as a DNA methylating agent.[5][6] The compound has no commercial value, in contrast to its isomer unsymmetrical dimethylhydrazine (1,1-dimethylhydrazine, UDMH), which is used as a rocket fuel.[7] Symmetrical dimethylhydrazine is more toxic than unsymmetrical dimethylhydrazine and is therefore an unwanted impurity in UDMH.[8]
It is used to induce colon tumors in experimental animals—particularly mice and feline cell samples.[2][9][10]
References
[edit]- ^ 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.
- ^ "1,2-Dimethylhydrazine". pubchem.ncbi.nlm.nih.gov. Retrieved 22 December 2021.
- ^ Salehi, Alireza; Hosseini, Seyed Mohammad; Kazemi, Sohrab (2022-06-23). "Antioxidant and Anticarcinogenic Potentials of Propolis for Dimethylhydrazine-Induced Colorectal Cancer in Wistar Rats". BioMed Research International. 2022: e8497562. doi:10.1155/2022/8497562. ISSN 2314-6133. PMC 9246617. PMID 35782078.
- ^ Valaei, Amirhasan; Azadeh, Fatemeh; Mostafavi Niaki, Seyedeh Talayeh; Salehi, Alireza; Shakib Khoob, Maede; Mirebrahimi, Seyed Hesam odin; Kazemi, Sohrab; Hosseini, Seyed Mohammad (2022-10-10). "Antioxidant and Anticancer Potentials of the Olive and Sesame Mixture against Dimethylhydrazine-Induced Colorectal Cancer in Wistar Rats". BioMed Research International. 2022: e5440773. doi:10.1155/2022/5440773. ISSN 2314-6133. PMC 9576397. PMID 36262974.
- ^ Gangadhar Choudhary, Hugh Hansen (August 1998). "Human health perspective of environmental exposure to hydrazines: A review". Chemosphere. 37 (5): 801–843. Bibcode:1998Chmsp..37..801C. doi:10.1016/S0045-6535(98)00088-5. PMID 9717244.
- ^ Schmidt, Eckart W. (2022). "Dimethylhydrazines". Encyclopedia of Liquid Fuels. De Gruyter. pp. 1333–1499. doi:10.1515/9783110750287-016. ISBN 978-3-11-075028-7.
- ^ Cruse, J. P.; Lewin, M. R.; Ferulano, G. P.; Clark, C. G. (December 1978). "Co-carcinogenic effects of dietary cholesterol in experimental colon cancer". Nature. 276 (5690): 822–5. Bibcode:1978Natur.276..822C. doi:10.1038/276822a0. PMID 723955. S2CID 4303843.
- ^ Wijnands, M.V.W. (April 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.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |