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A38207

Sigma-Aldrich

2-Aminoacetophenone hydrochloride

99%

Synonym(s):

ω-Aminoacetophenone hydrochloride, Phenacylamine hydrochloride

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About This Item

Linear Formula:
C6H5COCH2NH2 · HCl
CAS Number:
5468-37-1
Molecular Weight:
171.62
Beilstein/REAXYS Number:
3563173
EC Number:
226-787-2
MDL number:
MFCD00012873
UNSPSC Code:
12352100
PubChem Substance ID:
24890815
NACRES:
NA.22

assay

99%

form

crystals

mp

194 °C (dec.) (lit.)

SMILES string

Cl.NCC(=O)c1ccccc1

InChI

1S/C8H9NO.ClH/c9-6-8(10)7-4-2-1-3-5-7;/h1-5H,6,9H2;1H

InChI key

CVXGFPPAIUELDV-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Frank Sporkert et al.
Forensic science international, 133(1-2), 39-46 (2003-05-14)
A sensitive and reproducible method for the quantitative determination of cathinone (CTN), norpseudoephedrine (NPE, cathine) and norephedrine (NE) from hair was developed. The compounds were extracted for 4 hours with phosphate buffer pH 2.0, followed by a standard solid phase
[Anorexigenic activity of various derivatives of alpha-aminoacetophenone].
M S Sánchez et al.
Archivos de farmacologia y toxicologia, 5(3), 165-168 (1979-12-01)
Dopamine beta-hydroxylase: activity and inhibition in the presence of beta-substituted phenethylamines.
J P Klinman et al.
Biochemistry, 21(1), 67-75 (1982-01-05)
Yasumasa Iwai et al.
Chemical & pharmaceutical bulletin, 50(3), 441-443 (2002-03-26)
The new coupling reaction of phenacylamines with silylstannane and lithium diisopropylamide (LDA) is reported. The treatment of a phenacylamine iodide 1 with (trimethylsilyl)tributylstannane (Me3SiSnBu3) and cesium fluoride (CsF) gave a dimerization product 2 having no iodine atom. Reaction of 1
J B Mangold et al.
The Journal of biological chemistry, 259(12), 7772-7779 (1984-06-25)
Functionalization of the beta-carbon of phenethylamines has been shown to produce a new class of substrate/inhibitor of dopamine beta-monooxygenase. Whereas both beta-hydroxy- and beta- chlorophenethylamine are converted to alpha-aminoacetophenone at comparable rates, only the latter conversion is accompanied by concomitant
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