2'-aminoacetophenone hydrochloride

Names

[ Name ]:
2'-aminoacetophenone hydrochloride

[Synonym ]:
1-(2-Aminophenyl)ethanone hydrochloride (1:1)
1-(2-amino-phenyl)-ethanone,hydrochloride
EINECS 246-930-2
1-(2-aminophenyl)ethanonhydrochlorid
Ethanone, 1-(2-aminophenyl)-, hydrochloride (1:1)
MFCD00035477
1-(2-Aminophenyl)ethan-1-one hydrochloride
2'-Aminoacetophenone Hydrochloride
o-aminoacetophenone hydrochloride
orthoaminoacetophenone hydrochloride
1-(2-Aminophenyl)ethanone hydrochloride
2-Acetylaniliniumchlorid
Ethanone,1-(2-aminophenyl)-,hydrochloride (1:1)
Ethanone, 1-(2-aminophenyl)-, hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
251.8ºC at 760 mmHg

[ Melting Point ]:
285-289 °C(lit.)

[ Molecular Formula ]:
C₈H₁₀ClNO

[ Molecular Weight ]:
171.624

[ Flash Point ]:
106.1ºC

[ Exact Mass ]:
171.045090

[ PSA ]:
43.09000

[ LogP ]:
2.85460

[ Vapour Pressure ]:
0.0201mmHg at 25°C

MSDS

Click to get detail MSDS

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

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2922399090

[ Summary ]:
2922399090 other amino-aldehydes, amino-ketones and amino-quinones, other than those containing more than one kind of oxygen function; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Quantitative analysis of 2-aminoacetophenone in off-flavored wines by stable isotope dilution assay.

J. AOAC Int. 79(2) , 583-6, (1996)

Isotope dilution analysis was used to quantitate 2-aminoacetophenone in wines exhibiting the so-called untypical aging off-flavor. d3-Aminoacetophenone was synthesized and used as isotopomeric interna...

Glycosylation of aromatic amines III: Mechanistic implications of the pH-dependent glycosylation of various aromatic amines (kynurenine, 2'-aminoacetophenone, daptomycin, and sulfamethoxzaole).

J. Pharm. Sci. 98(12) , 4639-49, (2009)

Glycosylation reaction kinetics of a series of aromatic amines (kynurenine, 2'-aminoacetophenone, daptomycin, and sulfamethoxazole) was compared to propose a unifying reaction mechanism. Kinetic studi...

Purification and characterization of 2-aminoacetophenone reductase of newly isolated Burkholderia sp. YT.

J. Biosci. Bioeng. 104(5) , 416-9, (2007)

We found that a newly isolated Burkholderia sp. produced (R)-2-amino-1-phenylethanol from 2-aminoacetophenone, showing the high stereospecificity. NADPH-dependent 2-aminoacetophenone reductase purifie...