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SMB00019

Sigma-Aldrich

N-Acetyltyramine

≥95% (LC/MS-ELSD)

Synonym(s):

N-(2-(4-Hydroxyphenyl)ethyl)acetamide, N-(p-Hydroxyphenethyl)acetamide, N-Acetyl tyramine

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About This Item

Empirical Formula (Hill Notation):
C10H13NO2
CAS Number:
1202-66-0
Molecular Weight:
179.22
MDL number:
MFCD01670887
UNSPSC Code:
12352205
PubChem Substance ID:
329824672
NACRES:
NA.25

Assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

InChI

1S/C10H13NO2/c1-8(12)11-7-6-9-2-4-10(13)5-3-9/h2-5,13H,6-7H2,1H3,(H,11,12)

InChI key

ATDWJOOPFDQZNK-UHFFFAOYSA-N

Related Categories

General description

Natural product derived from fungal source.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Fengjun Shang et al.
Analytical chemistry, 81(10), 4089-4098 (2009-04-23)
N-acetyltyramine was synthesized and electropolymerized together with a negatively charged sulfobutylether-beta-cyclodextrin on a boron-doped diamond (BDD) electrode followed by the electropolymerization of pyrrole to form a stable and permselective film for selective dopamine detection. The selectivity and sensitivity of the
Reversal of resistance by N-acetyltyramine or N-acetyl-2-phenylethylamine in doxorubicin-resistant leukemia P388 cells.
S Kunimoto et al.
The Journal of antibiotics, 40(11), 1651-1652 (1987-11-01)
Y Endo
Biochimica et biophysica acta, 438(2), 532-539 (1976-07-08)
The enzyme catalyzing the deacetylaction of N-acetylhistamine was partially purified about 160-fold from rat liver extract and its properties were investigated. The purification procedure included DEAE-cellulose chromatography, precipitation with ammonium sulfate and DEAE-cellulose rechromatography. The enzyme contains a labile -SH
S Friström et al.
Acta pharmacologica et toxicologica, 40(2), 247-258 (1977-02-01)
The effect of five sympathomimetic amines and some of their acetyl derivatives on the blood pressure of the rat was determined on the left carotid artery. After pretreatment with chlorisondamine (1 mg/kg subcutaneously) the blood pressure rise by sympathomimetic amines
A K Mir et al.
Journal of neurochemistry, 36(2), 441-446 (1981-02-01)
N-Acetyltyramine, N-acetyldopamine and N-acetyloctopamine were the major products when either L-[3H]tyrosine or [3H]tyramine were incubated with thoracic ganglia of the desert locust, Schistocerca gregaria. No label was incorporated into L-DOPA under these conditions, although 2-3% of the radioactivity could be
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