Benzylamine | |
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1-Phenylmethanamine |
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Other names
α-Aminotoluene |
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Identifiers | |
CAS number | 100-46-9 |
ChemSpider | 7223 |
UNII | A1O31ROR09 |
DrugBank | DB02464 |
KEGG | C15562 |
ChEBI | CHEBI:40538 |
ChEMBL | CHEMBL522 |
RTECS number | DP1488500 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C7H9N |
Molar mass | 107.15 g mol−1 |
Appearance | Colorless liquid |
Density | 0.981 g/mL[1] |
Melting point |
10 °C, 283 K, 50 °F ([2]) |
Boiling point |
185 °C, 458 K, 365 °F ([2]) |
Solubility in water | Miscible[2] |
Acidity (pKa) | 9.34[3] |
Basicity (pKb) | 4.66 |
Refractive index (nD) | 1.543 |
Structure | |
Dipole moment | 1.38 D |
Hazards | |
MSDS | Fischer Scientific |
R-phrases | R21/22 R34[1] |
S-phrases | S26 S36/37/39 S45[1] |
Main hazards | Flammable |
NFPA 704 |
2
3
0
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Flash point | 65 °C (149 °F)[2][1] |
Related compounds | |
Related amines | aniline |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
Benzylamine is the chemical compound with the formula C6H5CH2NH2. It consists of a benzyl group, C6H5CH2, attached to an amine functional group. This colorless liquid is a common precursor in organic synthesis.
Benzylamine is preprared by hydrogenation of benzonitrile.
It is used as a masked source of ammonia, since after N-alkylation, the benzyl group can be removed by hydrogenolysis:[4]
Typically a base is employed in the first step to absorb the HBr (or related acid for other kinds of alkylating agents).