Benzylamine | |
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Esters [] | |
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Benzylamine acetate | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C7H9N[1] |
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Molecular mass | 107.15 g/mol[1] |
Density | 0.98 at 68 °F (USCG, 1999) - Less dense than water; will float g/cm3[1] |
Appearance | Colorless liquid[1] |
Odor | Ammonia-like odor[1] |
Predicted LogP | 1.1[1] |
Melting point | -51 °F (USCG, 1999)[1] |
Boiling point | 364.1 °[1] |
Decomposition | When heated to decomposition it emits toxic fumes.[1] |
Solubility | Miscible in ethanol and diethyl ether. Very soluble in acetone. Soluble in benzene. Slightly soluble in chloroform.[1] |
Chirality | achiral[2] |
Identifiers [] | |
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IUPAC name | phenylmethanamine[1] |
SMILES | C1=CC=C(C=C1)CN[1] |
InChI | InChI=1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-5H,6,8H2[1] |
InChIKey | WGQKYBSKWIADBV-UHFFFAOYSA-N[1] |
Dosing |
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Benzylamine
Benzylamine (also known as Monobenzylamine, (Phenylmethyl)amine, α-Aminotoluene, (Aminomethyl)benzene, 1-phenylmethanamine, N-Benzylamine, Moringine, Phenylmethylamine, Sumine 2005 or omega-Aminotoluene) is a substance of the benzylamine class.
Chemistry
Benzylamine is typically found in the form of its acetate ester.
Stereochemistry
Benzylamine is a achiral mixture