2-amino-2-methylpropanol
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | 2-amino-2-methylpropanol | |||||||||||||||
other names |
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Molecular formula | C 4 H 11 NO | |||||||||||||||
Brief description |
colorless solid with an amine-like odor |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 89.14 g mol −1 | |||||||||||||||
Physical state |
firmly |
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density |
0.93 g cm −3 |
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Melting point |
30 ° C |
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boiling point |
165 ° C |
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Vapor pressure |
2 mbar (30 ° C) |
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pK s value |
9.7 |
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solubility |
soluble in water |
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Refractive index |
1.448 (20 ° C) |
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safety instructions | ||||||||||||||||
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Toxicological data | ||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
2-Amino-2-methylpropanol is a chemical compound from the group of alcohols .
Extraction and presentation
2-Amino-2-methylpropanol can be obtained by reducing the corresponding nitro compound (which in turn can be obtained from 2-nitropropane and formaldehyde by the Henry reaction ).
properties
2-Amino-2-methylpropanol is a slightly volatile, colorless solid with an amine-like odor that is easily soluble in water.
use
2-Amino-2-methylpropanol is used in the manufacture of dyes and medicines .
Individual evidence
- ↑ Entry on AMINOMETHYL PROPANOL in the CosIng database of the EU Commission, accessed on February 16, 2020.
- ↑ a b c d e f g h i j k l Entry on 2-Amino-2-methylpropanol in the GESTIS substance database of the IFA , accessed on January 10, 2017(JavaScript required) .
- ↑ a b Data sheet 2-Amino-2-methyl-1-propanol from Sigma-Aldrich , accessed on May 21, 2017 ( PDF ).
- ↑ Entry on 2-amino-2-methylpropanol in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on August 1, 2016. Manufacturers or distributors can expand the harmonized classification and labeling .
- ↑ Entry on 2-Amino-2-methylpropanol in the Hazardous Substances Data Bank , accessed on November 12, 2012.