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Merck

PHR1680

Supelco

Desloratidine

Pharmaceutical Secondary Standard; Certified Reference Material

Synonim(y):

Desloratadine, 8-Chloro-6,11-dihydro-11-(4-piperidinylidene)-5H- benzo[5,6]cyclohepta[1,2,b]pyridine, Clarinex®, NSC 675447

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About This Item

Wzór empiryczny (zapis Hilla):
C19H19ClN2
Numer CAS:
Masa cząsteczkowa:
310.82
Numer MDL:
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
NACRES:
NA.24

klasa czystości

certified reference material
pharmaceutical secondary standard

Poziom jakości

agency

traceable to Ph. Eur. Y0001584
traceable to USP 1173042

rodzina API

desloratidine

Certyfikat analizy

current certificate can be downloaded

opakowanie

pkg of 1 g

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

pharmaceutical (small molecule)

format

neat

temp. przechowywania

2-30°C

ciąg SMILES

Clc1ccc2c(CCc3cccnc3\C2=C4\CCNCC4)c1

InChI

1S/C19H19ClN2/c20-16-5-6-17-15(12-16)4-3-14-2-1-9-22-19(14)18(17)13-7-10-21-11-8-13/h1-2,5-6,9,12,21H,3-4,7-8,10-11H2

Klucz InChI

JAUOIFJMECXRGI-UHFFFAOYSA-N

informacje o genach

human ... HRH1(3269)

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Opis ogólny

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.
Desloratadine is one of the orally active, highly selective peripheral H1 receptor antagonists that does not exert any significant effect on the central and autonomic nervous systems. The potency of desloratadine is more than that of loratadine and it exhibits substantial overall pharmacological profile.

Zastosowanie

Desloratadine may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations and plasma samples by various chromatography techniques.
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.

Działania biochem./fizjol.

Desloratadine is a selective and nonsedating histamine H1 receptor antagonist, an active metabolite of loratadine (Claritin), used to relieve hay fever and allergy symptoms with less drowsiness than other antihistamines; does not significantly inhibits cardiac K+ channels at clinically achievable blood levels. Free from antimuscarinic/anticholinergic effects.

Komentarz do analizy

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

Inne uwagi

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.

Przypis

To see an example of a Certificate of Analysis for this material enter LRAC2775 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

Polecane produkty

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.

Informacje prawne

Clarinex is a registered trademark of Schering Corp.
This page may contain text that has been machine translated.

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

390.2 °F - Pensky-Martens closed cup

Temperatura zapłonu (°C)

199 °C - Pensky-Martens closed cup


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Certyfikaty analizy (CoA)

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Klienci oglądali również te produkty

Spectrophotometric, spectrofluorometric and HPLC determination of desloratadine in dosage forms and human plasma.
El-Enany N, et al.
Chemical & Pharmaceutical Bulletin, 55(12), 1662-1670 (2007)
High-performance liquid chromatographic method for the bioequivalence evaluation of desloratadine fumarate tablets in dogs.
Liu L, et al.
Journal of Pharmaceutical and Biomedical Analysis, 34(5), 1013-1019 (2004)
A validated stability-indicating UPLC method for desloratadine and its impurities in pharmaceutical dosage forms.
Rao DD, et al.
Journal of Pharmaceutical and Biomedical Analysis, 51(3), 736-742 (2010)
Determination of desloratadine in drug substance and pharmaceutical preparations by liquid chromatography.
Qi M, et al.
Journal of Pharmaceutical and Biomedical Analysis, 38(2), 355-359 (2005)

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