Urea
the diamide of carbonic acid
Urea is an organic compound. It was first found in urine in 1773 by the French chemist Jean Rouelle. It is also called Carbamide, and its chemical names are Carbonyl Diamide (used in inorganic chemistry) and Diaminomethanal (used in organic chemistry).
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| Names | |||
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| IUPAC name
Aminomethylamide
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| Other names
Carbamide
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| Identifiers | |||
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3D model (JSmol)
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| ChemSpider | |||
| ECHA InfoCard | 100.000.286 | ||
| E number | E927b (glazing agents, ...) | ||
CompTox Dashboard (EPA)
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| Properties | |||
| (NH2)2CO | |||
| Molar mass | 60.07 g/mol | ||
| Appearance | white odourless solid | ||
| Density | 1.33·10³ kg/m³,[1] solid | ||
| Melting point | 132.7 °C (406 K) decomposes | ||
| Boiling point | n.a. | ||
| 108 g/100 ml (20 °C) 167 g/100 ml (40 °C) 251 g/100 ml (60 °C) 400 g/100 ml (80 °C) 733 g/100 ml (100 °C) | |||
| Acidity (pKa) | 0.18 | ||
| Basicity (pKb) | 13.82 | ||
| Structure | |||
| 4.56 p/D | |||
| Hazards | |||
| MSDS | ScienceLab.com | ||
| NFPA 704 |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
| Infobox references | |||
In humans, it is a normal component of blood and many body tissues. It is produced in the liver, where ammonia, a very toxic substance, is changed into urea, which has a very low toxicity, so low in fact, that it is many times less toxic than table salt. Most of the urea produced in this way is not needed by the body, and is removed from the blood in the kidneys and taken out of the body in urine.
References change
Other websites change
- MSDS sheet on urea Archived 2011-05-15 at the Wayback Machine
- Use of urea in hand dyeing
- use of urea as an automotive reagent to reduce harmful emissions (AdBlue)
- The dispensing and handling of Urea AdBlue (AdBlue Archived 2016-06-30 at the Wayback Machine)
