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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:
Molecular Weight:
123.15
Beilstein:
2205844
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

92-95 °C (lit.)

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

Signal Word

Warning

Hazard Statements

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

Certificates of Analysis (COA)

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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)
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
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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