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PHR2006

Allopurinol Related Compound B

Pharmaceutical Secondary Standard; Certified Reference Material

Synonim(y):

3-(Formylamino)-1H-pyrazole-4-carboxamide, 5-(Formylamino)-1H-pyrazole-4-carboxamide

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Rozmiar/SKUDostępnośćCena netto
50 mg
Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności
2910,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C5H6N4O2
Numer CAS:
Masa cząsteczkowa:
154.13
UNSPSC Code:
41116107
NACRES:
NA.24

2910,00 zł


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Quality Segment

grade

certified reference material, pharmaceutical secondary standard

agency

traceable to Ph. Eur. A0350020, traceable to USP 1013013

API family

allopurinol

CofA

current certificate can be downloaded

packaging

pkg of 50 mg

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

SMILES string

[nH]1ncc(c1NC=O)C(=O)N

InChI

1S/C5H6N4O2/c6-4(11)3-1-8-9-5(3)7-2-10/h1-2H,(H2,6,11)(H2,7,8,9,10)

InChI key

MKVXRGIJTKYXPR-UHFFFAOYSA-N

General description

Allopurinol Related Compound B 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

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.
Allopurinol Related Compound B may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by chromatography.

Analysis Note

These secondary standards offer multi-traceability to the USP and EP 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.
To see an example of a Certificate of Analysis for this material enter LRAB7872 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.
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Ta pozycja
1013013A0350020BP832
description

Pharmaceutical Secondary Standard; Certified Reference Material

description

United States Pharmacopeia (USP) Reference Standard

description

European Pharmacopoeia (EP) Reference Standard

description

British Pharmacopoeia (BP) Reference Standard

application(s)

pharmaceutical

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical
pharmaceutical small molecule

format

neat

format

neat

format

neat

format

neat

Quality Level

300

Quality Level

-

Quality Level

-

Quality Level

-

grade

certified reference material, pharmaceutical secondary standard

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

packaging

pkg of 50 mg

packaging

-

packaging

-

packaging

-


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Klasa składowania

11 - Combustible Solids

Co się dzieje?

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable



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Certyfikaty analizy (CoA)

Lot/Batch Number

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