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858897

Sigma-Aldrich

Nω-Acetylhistamine

98%

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About This Item

Empirical Formula (Hill Notation):
C7H11N3O
CAS Number:
673-49-4
Molecular Weight:
153.18
EC Number:
211-610-3
MDL number:
MFCD00005209
UNSPSC Code:
12352005
eCl@ss:
32160406
PubChem Substance ID:
24888477
NACRES:
NA.22

Quality Level

100

Assay

98%

form

solid

mp

147-149 °C (lit.)

functional group

amide

SMILES string

CC(=O)NCCc1c[nH]cn1

InChI

1S/C7H11N3O/c1-6(11)9-3-2-7-4-8-5-10-7/h4-5H,2-3H2,1H3,(H,8,10)(H,9,11)

InChI key

XJWPISBUKWZALE-UHFFFAOYSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

858897-BULK:
858897-VAR:
858897-1G:
858897-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKAA2296V
MKAA2296
08413JI
12404MA
07105AI

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K Uchida et al.
Biochimica et biophysica acta, 991(2), 377-379 (1989-05-31)
In the presence of molecular oxygen and a catalytic amount of copper(II) ion, ascorbate almost completely degraded histamine (approx. 72%). The reaction was shown to occur at the imidazole group but not at the primary amino group in histamine. 4-[2-(Acetylamino)ethyl]-2,3-dihydroimidazol-2-one
[Molecular mechanism of the interaction of histamine with hyaluronic acid].
K L Erzinkian et al.
Izvestiia Akademii nauk SSSR. Seriia biologicheskaia, (2)(2), 206-210 (1985-03-01)
L R Hegstrand et al.
Journal of neurochemistry, 45(1), 300-307 (1985-07-01)
Properties of N-acetylhistamine deacetylase in rat brain were studied, utilizing a sensitive coupled radioenzymatic assay. The Km for N-acetylhistamine for this deacetylase was 660 microM and its Vmax was 330 pmol/h/mg protein. N-Acetylhistamine deacetylase activity increased 80% in the presence
K Onodera et al.
Methods and findings in experimental and clinical pharmacology, 16(8), 575-581 (1994-10-01)
The purpose of this study was to examine the effects of intracerebroventricular (i.c.v.) administration of N-acetylhistamine on rectal temperature, histamine level, histidine decarboxylase (HDC) activity, and the turnover rate of monoamines in mice. More than 60 micrograms of N-acetylhistamine induced
V Gabermann
Farmakologiia i toksikologiia, 44(2), 220-224 (1981-03-01)
Oscillographic polarography in an alkaline medium has shown that the alkaloid N-isovalerylhistamine appears as an expressive wave of the adsorption character in the cathode portion of the curve. This makes it possible to detect it at concentrations up to 10(-6)
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Global Trade Item Number

SKUGTIN
858897-1G4061826664957
858897-5G

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