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Merck

M7780

Supelco

3-Methylhistamin -dihydrochlorid

analytical standard

Synonym(e):

3-Methyl-4-(β-amino-ethyl)-imidazol

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About This Item

Empirische Formel (Hill-System):
C6H11N3 · 2HCl
CAS-Nummer:
Molekulargewicht:
198.09
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

Format

neat

Lagertemp.

2-8°C

SMILES String

Cl.Cl.Cn1cncc1CCN

InChI

1S/C6H11N3.2ClH/c1-9-5-8-4-6(9)2-3-7;;/h4-5H,2-3,7H2,1H3;2*1H

InChIKey

KWEIZIDNCJBKIY-UHFFFAOYSA-N

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Analysenzertifikate (COA)

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T Iwashina et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 48(9), 1187-1191 (1998-01-07)
In order to trace the loss of N tau-methylhistamine, a principal metabolite of histamine, during extraction and purification from human plasma and urine samples, N tau-[3H]methylhistamine was prepared in two steps from N alpha t-butoxycarbonylhistamine (II). In the first step
Tibor Mikó et al.
Journal of medicinal chemistry, 46(8), 1523-1530 (2003-04-04)
In an extension of very recently published studies on successful imidazole replacements in some series of histamine H(3) receptor antagonists, we report on a new class of lipophilic nonimidazole antagonist having an aliphatic tertiary amino moiety connected to a benzyl
S Reidemeister et al.
Die Pharmazie, 55(2), 83-86 (2000-03-21)
Novel substituted N-phenylcarbamates as derivatives of 3-(1 H-imidazol-4-yl)propanol were prepared and tested for their antagonist potency in vitro and in vivo at histamine H3 receptors. Structural modifications with different alkyl and acetyl moieties were performed in an attempt to optimize
S Murray et al.
Journal of chromatography, 567(2), 289-298 (1991-07-05)
An assay has been developed for N tau-methylhistamine, a major metabolite of the autocoid histamine, based on gas chromatography-electron-capture negative-ion chemical ionisation mass spectrometry. N tau-Methylhistamine was extracted from urine by cation-exchange chromatography and converted to its di-(3,5-bistrifluoromethylbenzoyl) derivative. The
J C Fitzpatrick et al.
The Journal of surgical research, 49(4), 293-297 (1990-10-01)
Carcinine (beta-alanylhistamine) is an imidazole dipeptide that exists in mammalian hearts, increases cardiac contractility, and is metabolically linked to carnosine (beta-alanylhistidine), a non-mast cell histidine and histamine precursor during stress. We have previously shown that tissue carnosine levels are regulated

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