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PHR1181

Supelco

2-Methylimidazole (Ondansetron Impurity F)

Pharmaceutical Secondary Standard; Certified Reference Material

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Synonym(s):
2-Methylimidazole, Ondansetron impurity F, 2-Methylglyoxaline
Empirical Formula (Hill Notation):
C4H6N2
CAS Number:
693-98-1
Molecular Weight:
82.10
Beilstein:
1368
EC Number:
211-765-7
MDL number:
MFCD00005190
UNSPSC Code:
41116107
PubChem Substance ID:
329823193
NACRES:
NA.24

grade

certified reference material
pharmaceutical secondary standard

Quality Level

100

Agency

traceable to Ph. Eur. Y0001320

vapor pressure

<1 mmHg ( 0 °C)

API family

ondansetron

CofA

current certificate can be downloaded

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

267-268 °C (lit.)

mp

142-143 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

SMILES string

Cc1ncc[nH]1

InChI

1S/C4H6N2/c1-4-5-2-3-6-4/h2-3H,1H3,(H,5,6)

InChI key

LXBGSDVWAMZHDD-UHFFFAOYSA-N

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General description

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

Application

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Analysis Note

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAA9000 in the slot below. This is an example certificate only and may not be the lot that you receive.

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Signal Word

Danger

Hazard Statements

H302,H314,H351,H360Df

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1C

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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Jerry D Johnson et al.
Journal of toxicology and environmental health. Part A, 65(12), 869-879 (2002-06-25)
The toxicokinetics of 2-methylimidazole (2-MI) were studied in male and female Fischer 344 rats after a single iv dose of 10 mg/kg or gavage dose of 25, 50, or 100 mg/kg. The 2-MI was formulated in 0.05 M phosphate-buffered saline
M van Gastel et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 4(3), 257-265 (1999-08-10)
Frozen solutions of the azurin mutant His117Gly in the presence of excess of methyl-substituted imidazoles have been investigated by electron spin-echo envelope modulation (ESEEM) spectroscopy at 9 GHz. The addition of imidazole is known to reconstitute a blue-copper site and
P C Chan et al.
Archives of toxicology, 82(6), 399-412 (2007-10-10)
2-Methylimidazole (2MI) has been identified as a by-product of fermentation and is detected in foods and mainstream and side-stream tobacco smoke. It is used in the manufacture of pharmaceuticals, photographic chemicals, dyes and pigments, agricultural chemicals, and rubber. Carcinogenicity studies
Cristina Maccallini et al.
Bioorganic & medicinal chemistry letters, 20(22), 6495-6499 (2010-10-12)
A series of N-substituted acetamidines and 2-methylimidazole derivatives structurally related to W1400 were synthesized and evaluated as Nitric Oxide Synthase (NOS) inhibitors. Analogs with sterically hindering isopropyl and phenyl substituents on the benzylic carbon connecting the aromatic core of W1400
Jiafeng Geng et al.
Journal of the American Chemical Society, 134(29), 12209-12218 (2012-06-30)
Tryptophan 2,3-dioxygenase (TDO) is a heme-dependent enzyme that catalyzes the oxidative degradation of L-tryptophan (L-Trp) to N-formylkynurenine (NFK). A highly conserved histidine residue in the distal heme pocket has attracted great attention in the mechanistic studies of TDO. However, a
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