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Merck
CN

191396

3-Aminobenzyl alcohol

97%

Synonym(s):

3-(Hydroxymethyl)aniline

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About This Item

Linear Formula:
H2NC6H4CH2OH
CAS Number:
Molecular Weight:
123.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-514-8
Beilstein/REAXYS Number:
2205844
MDL number:
Assay:
97%
Form:
solid
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Quality Level

assay

97%

form

solid

mp

92-95 °C (lit.)

functional group

hydroxyl

SMILES string

Nc1cccc(CO)c1

InChI

1S/C7H9NO/c8-7-3-1-2-6(4-7)5-9/h1-4,9H,5,8H2

InChI key

OJZQOQNSUZLSMV-UHFFFAOYSA-N



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pictograms

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signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Nicolas Bridiau et al.
Biotechnology progress, 22(1), 326-330 (2006-02-04)
A new approach to galacto-oligosaccharides and galacto-conjugates synthesis performed by the beta-galactosidase from Kluyveromyces lactis is reported. The enzymatic galactosylation of eight kinds of adsorbed aromatic primary alcohols, in particular the two drugs guaifenesin and chlorphenesin, gave the corresponding beta-D-galacto-pyranosides
Synthesis and characterization of new 2-(alkylamino) acetamides.
Mancilla T, et al.
ARKIVOC (Gainesville, FL, United States), 11, 37-47 (2003)
N Sundaraganesan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(11), 2511-2517 (2003-09-10)
The laser Raman and FTIR spectra of 3-aminobenzyl alcohol have been recorded. The observed frequencies were assigned to various modes of vibrations on the basis of normal coordinate analysis, assuming C(s) point group symmetry. The potential energy distribution associated with



Global Trade Item Number

SKUGTIN
191396-10G04061838760197
191396-25G04061832279244