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Documenti fondamentali

PHR1576

Supelco

Pirazinacarbossammide

Pharmaceutical Secondary Standard; Certified Reference Material

Sinonimo/i:

Ammide dell’acido pirazinoico, Pirazinamide

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About This Item

Formula empirica (notazione di Hill):
C5H5N3O
Numero CAS:
Peso molecolare:
123.11
Beilstein:
112306
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

certified reference material
pharmaceutical secondary standard

Livello qualitativo

agenzia

traceable to BP 906
traceable to Ph. Eur. P4050000
traceable to USP 1585006

Famiglia di API

pyrazinamide

CdA

current certificate can be downloaded

Confezionamento

pkg of 500 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

189-191 °C (lit.)

applicazioni

pharmaceutical (small molecule)

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

NC(=O)c1cnccn1

InChI

1S/C5H5N3O/c6-5(9)4-3-7-1-2-8-4/h1-3H,(H2,6,9)
IPEHBUMCGVEMRF-UHFFFAOYSA-N

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Descrizione generale

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.
Pyrazinamide is an analog of nicotinamide. It is an antituberculosis drug and plays a vital role in reducing the duration of chemotherapy of tuberculosis.

Applicazioni

Pyrazinamide may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by liquid chromatography and multivariate spectrophotometry.
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.

Risultati analitici

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

Altre note

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.

Nota a piè di pagina

To see an example of a Certificate of Analysis for this material enter LRAA4492 in the slot below. This is an example certificate only and may not be the lot that you receive.

Prodotti consigliati

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

Lot/Batch Number

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Lomustine United States Pharmacopeia (USP) Reference Standard

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1369419

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Isoniazide European Pharmacopoeia (EP) Reference Standard

I0500000

Isoniazide

Isoniazide analytical standard, ≥99% (TLC)

Supelco

I3377

Isoniazide

Rifampicin ≥95% (HPLC), powder or crystals

Sigma-Aldrich

R3501

Rifampicin

Liquid chromatographic determination of isoniazid, pyrazinamide and rifampicin from pharmaceutical preparations and blood.
Khuhawar MY and Rind FMA
Journal of Chromatography. B, Biomedical Sciences and Applications, 766(2), 357-363 (2002)
Simultaneous determination of rifampicin, isoniazid and pyrazinamide in tablet preparations by multivariate spectrophotometric calibration.
Goicoechea HC and Olivieri AC
Journal of Pharmaceutical and Biomedical Analysis, 20(4), 681-686 (1999)
Validation of a RP-LC method for the simultaneous determination of isoniazid, pyrazinamide and rifampicin in a pharmaceutical formulation.
Calleri E, et al.
Journal of Pharmaceutical and Biomedical Analysis, 29(6), 1089-1096 (2002)

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