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PHR1857

Supelco

Sitagliptina

Pharmaceutical Secondary Standard; Certified Reference Material

Sinônimo(s):

7-[(3R)-3-amino-1-oxo-4-(2,4,5-trifluorofenil)butil]-5,6,7,8-tetra-hidro-3-(trifluorometil)-1,2,4-triazolo[4,3-a]pirazina fosfato, MK-0431

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About This Item

Fórmula empírica (Notação de Hill):
C16H15F6N5O · H3PO4 · H2O
Número CAS:
Peso molecular:
523.32
Código UNSPSC:
41116107
NACRES:
NA.24

grau

certified reference material
pharmaceutical secondary standard

Nível de qualidade

Agency

traceable to Ph. Eur. Y0001812
traceable to USP 1612903

família API

sitagliptin

forma

powder

Certificado de análise (CofA)

current certificate can be downloaded

embalagem

pkg of 1 g

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

pharmaceutical (small molecule)

temperatura de armazenamento

2-8°C

InChI

1S/C16H15F6N5O.H3O4P.H2O/c17-10-6-12(19)11(18)4-8(10)3-9(23)5-14(28)26-1-2-27-13(7-26)24-25-15(27)16(20,21)22;1-5(2,3)4;/h4,6,9H,1-3,5,7,23H2;(H3,1,2,3,4);1H2/t9-;;/m1../s1

chave InChI

GQPYTJVDPQTBQC-KLQYNRQASA-N

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Descrição geral

Medicamento antidiabético (anti-hiperglicêmico) da classe da dipeptidil peptidase-4 (DPP-4). Acredita-se que a inibição da enzima DPP-4 aumente o peptídeo semelhante ao glucagon 1 (GLP-1), o que inibe a liberação de glucagon, estimula a liberação de insulina e diminui a glicemia.
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.

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.

Sitagliptin phosphate, a dipeptidyl peptidase IV (DPPIV) inhibitor, is an antidiabetic drug used in the treatment of diabetes type II mellitus.

Aplicação

This pharmaceutical secondary standard can also be used as follows:
  • Development of a reversed-phase high-performance liquid chromatographic (RP-HPLC) method to determine sitagliptin phosphate and metformin hydrochloride in combined pharmaceutical formulations
  • 19F nuclear magnetic resonance (19F-NMR) spectroscopy-based quantitative analysis of sitagliptin phosphate and validation of the method using proton 1H-NMR
  • Determination of sitagliptin phosphate in tablet dosage forms using RP-HPLC and following International Conference on Harmonization (ICH) guidelines
  • Simultaneous estimation of sitagliptin and four of its impurities in pharmaceutical formulations by micellar electrokinetic chromatography (MEKC) following a quality-by-design (QbD) approach
  • Multi-analysis of sitagliptin phosphate, metformin hydrochloride, pioglitazone hydrochloride, gliclazide, glibenclamide, and repaglinide in pharmaceutical tablets using reversed phase-liquid chromatography (RP-LC)

Nota de análise

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

Nota de rodapé

To see an example of a Certificate of Analysis for this material enter LRAC0251 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

Pictogramas

Health hazardExclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - STOT RE 2

Órgãos-alvo

Liver

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Certificados de análise (COA)

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Os clientes também visualizaram

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A validated HPLC stability indicating method for the determination of sitagliptin in bulk drug substance and tablets
Qassas MK, et al.
International Journal of Pharmaceutical Sciences Review and Research, 32, 194-198 (2015)
Validated liquid chromatographic method for simultaneous determination of metformin, pioglitazone, sitagliptin, repaglinide, glibenclamide and gliclazide-application for counterfeit drug analysis
Elkady EF, et al.
Journal of Analytical and Bioanalytical Techniques , 1-1 (2015)

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