Dimethylurea
Names | |
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Preferred IUPAC name
N,N′-Dimethylurea | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.002.272 |
KEGG | |
MeSH | 1,3-dimethylurea |
PubChem CID
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RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C3H8N2O | |
Molar mass | 88.110 g·mol−1 |
Appearance | Colorless, waxy crystals |
Odor | Odorless |
Density | 1.142 g mL−1 |
Melting point | 104.4 °C; 219.8 °F; 377.5 K |
Boiling point | 269.1 °C; 516.3 °F; 542.2 K |
765 g L−1 | |
-55.1·10−6 cm3/mol | |
Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
−312.1–−312.1 kJ mol−1 |
Std enthalpy of
combustion (ΔcH⦵298) |
−2.0145–−2.0089 MJ mol−1 |
Hazards | |
R-phrases (outdated) | H373[1] R22, R24/25 |
S-phrases (outdated) | P260, P314, P501H373[1] |
Flash point | 157 °C (315 °F; 430 K) |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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4 g kg−1 (oral, rat) |
Related compounds | |
Related ureas
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Carmustine |
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). | |
what is ?) | (|
Infobox references | |
Dimethylurea (DMU) (IUPAC systematic name: 1,3-Dimethylurea ) is a urea derivative and used as an intermediate in organic synthesis. It is a colorless crystalline powder with little toxicity.
Uses[]
1,3-Dimethylurea is used for synthesis of caffeine, theophylline, pharmachemicals, textile aids, herbicides and others.[2] In the textile processing industry 1,3-dimethylurea is used as intermediate for the production of formaldehyde-free easy-care finishing agents for textiles. The estimated world production of DMU is estimated to be less than 25,000 tons.
References[]
- ^ Jump up to: a b "1,3-dimethylurea - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 26 March 2005. Identification. Retrieved 10 April 2012.
- ^ http://www.inchem.org/documents/sids/sids/96311.pdf SIDS Initial Assessment Report
Categories:
- Ureas