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191396

Sigma-Aldrich

3-Aminobenzyl alcohol

97%

Synonym(s):

3-(Hydroxymethyl)aniline

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About This Item

Linear Formula:
H2NC6H4CH2OH
CAS Number:
1877-77-6
Molecular Weight:
123.15
Beilstein:
2205844
EC Number:
217-514-8
MDL number:
MFCD00007817
UNSPSC Code:
12352100
PubChem Substance ID:
24851484
NACRES:
NA.22
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Quality Level

100

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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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBG1733V
STBC5631V
MKBG6198V
S44554V
MKBB7764

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Synthesis and fungicidal activity of N-[4-(4-fluoro) phenyl-2-piperidin-4-yl-thiazol-5-yl] pyrimidin-2-yl-N-phenylamines on Phytophthora capsici.
Choi W-S, et al.
Journal of the Korean Society for Applied Biological Chemistry, 53(2), 206-214 (2010)
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
Synthesis and characterization of new 2-(alkylamino) acetamides.
Mancilla T, et al.
ARKIVOC (Gainesville, FL, United States), 11, 37-47 (2003)
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
Anton Georgiev et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 175, 76-91 (2016-12-27)
In this paper three different "push-pull" 4-aminoazobenzene dyes have been synthesized in order to characterize their photochromic behavior in different solvents. The molecular geometry was optimized by DFT/B3LYP functional combined with the standard 6-31+G(d,p) basis set for trans (E) and

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