W390607
2′-氨基苯乙酮
≥98%
别名:
2-乙酰苯胺
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关于此项目
线性分子式:
H2NC6H4COCH3
化学文摘社编号:
分子量:
135.16
Flavis number:
11.008
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3906
NACRES:
NA.21
EC Number:
209-002-8
MDL number:
Beilstein/REAXYS Number:
386122
Organoleptic:
grape
Grade:
Halal, Kosher
Biological source:
synthetic
Food allergen:
no known allergens
InChI key
GTDQGKWDWVUKTI-UHFFFAOYSA-N
InChI
1S/C8H9NO/c1-6(10)7-4-2-3-5-8(7)9/h2-5H,9H2,1H3
SMILES string
CC(=O)c1ccccc1N
biological source
synthetic
grade
Halal, Kosher
assay
≥98%
refractive index
n20/D 1.614 (lit.)
bp
85-90 °C/0.5 mmHg (lit.)
density
1.112 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
grape
storage temp.
2-8°C
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General description
2′-氨基苯乙酮是玉米面粉产品中关键的挥发性风味成分之一。{9]据报道，其也是造成铜绿假单胞菌生长的培养基中葡萄样气味的原因。
Disclaimer
仅供R&D或非EU食品使用不用于零售。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Use of 2-aminoacetophenone production in identification of Pseudomonas aeruginosa.
Cox CD & Parker J.
Journal of Clinical Microbiology, 9(4), 479-484 (1979)
Hans-Georg Schmarr et al.
Journal of chromatography. A, 1150(1-2), 78-84 (2006-10-04)
The key compound in the wine off-flavor phenomenon "Untypische Alterungsnote" (UTA) is 2-aminoacetophenone (AAP). A new method for its quantitative analysis in wine is described. The analysis is based on solid phase extraction with LiChrolut EN as sorbent material followed
Michael C Myers et al.
Journal of the American Chemical Society, 127(17), 6152-6153 (2005-04-28)
Cells that express mutant p53 derived from cancers are selectively killed by a new class of small organic molecules. The protein p53 is recognized as one of the most important guardians in the body that prevents tumor development. Mutant forms
Madhushree Y Gokhale et al.
Journal of pharmaceutical sciences, 98(12), 4639-4649 (2009-06-25)
Glycosylation reaction kinetics of a series of aromatic amines (kynurenine, 2'-aminoacetophenone, daptomycin, and sulfamethoxazole) was compared to propose a unifying reaction mechanism. Kinetic studies were conducted in aqueous solutions containing glucose in the pH range 1-6.5 with 2'-aminoacetophenone and daptomycin.
Guogang Zhao et al.
Biotechnology letters, 26(16), 1255-1259 (2004-10-16)
A new isolate of Arthrobacter sulfureus , when incubated at 50 g resting cells (dry cell wt) l(-1) with 50 g glucose l(-1) and 1 g 2-aminoacetophenone l(-1) in 50 mm potassium buffer (pH 7, 4 ml) at 30 degrees
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