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PHR2009

Supelco

Allopurinol Related Compound E

Pharmaceutical Secondary Standard; Certified Reference Material

Synonym(s):

Ethyl 3-(formylamino)-1H-pyrazole-4-carboxylate, Ethyl 5-(formylamino)-1H-pyrazole-4-carboxylate

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About This Item

Empirical Formula (Hill Notation):
C7H9N3O3
CAS Number:
Molecular Weight:
183.16
UNSPSC Code:
41116107
NACRES:
NA.24

grade

certified reference material
pharmaceutical secondary standard

Quality Level

Agency

traceable to BP 845
traceable to Ph. Eur. A0350050
traceable to USP 1013068

API family

allopurinol

CofA

current certificate can be downloaded

packaging

pkg of 50 mg

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

InChI

1S/C7H9N3O3/c1-2-13-7(12)5-3-9-10-6(5)8-4-11/h3-4H,2H2,1H3,(H2,8,9,10,11)

InChI key

VAEIHNPPOAVFAR-UHFFFAOYSA-N

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General description

Allopurinol Related Compound E is an impurity of allopurinol. Allopurinol is a purine analog and a structural isomer of the naturally available purine in the body, hypoxanthine. It is also a powerful xanthine oxidase inhibitor. It is widely utilized against purine and pyrimidine metabolic disorders that give rise to an excess of uric acid in humans.
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

Allopurinol Related Compound E may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by chromatography.
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 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 LRAB7871 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Certificates of Analysis (COA)

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Allopurinol
USP42-NF37: United States Pharmacopeia and National Formulary
United States Pharmacopeia/National Formulary, 34(1), 132-132 (2018)
High-performance liquid chromatography with polarographic and voltammetric anodic detection: simultaneous determination of allopurinol, oxipurinol and uric acid in body fluids
Palmisano F, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 306(1), 205-214 (1984)
Development of a stability indicating RP-RRLC method for determination of allopurinol and its degradation products in solid oral dosage
Singh S and Gadhawala Z
International Journal of PharmTech Research, 5(1), 44-53 (2013)

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