2-Aminobenzyl alcohol

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Names

[ CAS No. ]:
1877-77-6

[ Name ]:
2-Aminobenzyl alcohol

[Synonym ]:
M-AMINOBENZYL ALCOHOL
3-(Hydroxymethyl)aniline
Benzenemethanol, 2-amino-
Benzenemethanol, 3-amino-
3-Aminobenzyl alcohol
MFCD00007817
EINECS 217-514-8
Benzenemethanol,3-amino
3-Aminobenzenemethanol
3-Aminobenzylalcohol
2-Aminobenzyl alcohol
3-aminophenylmethanol
(3-Aminophenyl)methanol
ZR C1Q
Benzyl alcohol,m-amino
(2-Aminophenyl)methanol
m-hydroxymethylphenyl amine

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
290.7±15.0 °C at 760 mmHg

[ Melting Point ]:
92-95 °C(lit.)

[ Molecular Formula ]:
C7H9NO

[ Molecular Weight ]:
123.152

[ Flash Point ]:
129.6±20.4 °C

[ Exact Mass ]:
123.068413

[ PSA ]:
46.25000

[ LogP ]:
-0.25

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.617

[ Storage condition ]:
2-8°C

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
DN3154450
CHEMICAL NAME :
Benzyl alcohol, m-amino-
CAS REGISTRY NUMBER :
1877-77-6
BEILSTEIN REFERENCE NO. :
2205844
LAST UPDATED :
199612
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C7-H9-N-O
MOLECULAR WEIGHT :
123.17

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Morphological transformation
TEST SYSTEM :
Rodent - hamster Embryo
DOSE/DURATION :
8 mmol/L
REFERENCE :
CALEDQ Cancer Letters (Shannon, Ireland). (Elsevier Scientific Pub. Ireland Ltd., POB 85, Limerick, Ireland) V.1- 1975- Volume(issue)/page/year: 52,203,1990

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
UN2811

[ WGK Germany ]:
3

[ RTECS ]:
DN3154450

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
29221980

Synthetic Route

Precursor & DownStream

Precursor

  • 3-Nitrobenzaldehyde
  • 3-Nitrobenzenemethanol
  • 3-Aminobenzoic acid
  • 3-Cyanobenzaldehyde
  • 3-Formylaniline
  • N-Boc-3-hydroxymethylaniline
  • 3-(Hydroxymethyl)phenylboronic acid
  • 3-nitrosobenzaldehyde
  • 3-Nitrobenzoic acid

DownStream

  • 3-(chloromethyl)-2,4,6-triiodoaniline
  • 2,6-DICHLORO-4-NITROANISOLE
  • 3-Amino-2,4,6-triiodobenzyl alcohol
  • 9H-fluoren-9-ylmethyl N-(3-formylphenyl)carbamate
  • 2,4-Dinitroaniline
  • 3-(Hydroxymethyl)benzonitrile
  • 3-(hydroxymethyl)benzoic acid
  • 3-METHOXYMETHYLANILINE
  • 3-(BROMOMETHYL)-BENZENAMINE

Customs

[ HS Code ]: 2922199090

[ Summary ]:
2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Beta-galactosidase catalyzed selective galactosylation of aromatic compounds.

Biotechnol. Prog. 22(1) , 326-30, (2006)

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 a...

Vibrational spectra, assignments and normal coordinate analysis of 3-aminobenzyl alcohol.

Spectrochim. Acta. A. Mol. Biomol. Spectrosc. 59(11) , 2511-7, (2003)

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...

Synthesis and characterization of new 2-(alkylamino) acetamides. Mancilla T, et al.

ARKIVOC 11 , 37-47, (2003)


More Articles


Related Compounds

  • 2-Aminobenzyl alcohol
  • N-Boc-2-aminobenzyl alcohol
  • N-acetyl-2-aminobenzyl alcohol
  • N-acetyl-O-acetyl-2-aminobenzyl alcohol
  • N-benzyloxycarbonyl-2-aminobenzyl alcohol
  • 2-(Diphenylamino)benzenemethanol
  • N-(5-Iodo-1,3,4-thiadiazol-2-yl)acetamide
  • tert-Butyl 4-iodo-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate
  • (7-Bromo-4-fluoro-1H-indol-3-yl)methanamine
  • Ethyl benzo[c][1,2,5]oxadiazole-4-carboxylate
  • tert-Butyl 3-(3-chlorophenyl)-3-oxopropanoate
  • 5-Chloro-2-methyl-6-(trifluoromethyl)pyrimidin-4-amine
  • 3,3-Dimethyl-1H-pyrido[3,4-b][1,4]oxazin-2(3H)-one
  • 3-(2,2,2-Trifluoroethoxy)isonicotinaldehyde
  • Methyl 2-(tetrahydro-2H-pyran-4-yl)thiazole-4-carboxylate
  • tert-Butyl (2-(tetrahydro-2H-thiopyran-4-yl)thiazol-4-yl)carbamate
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