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PHR2020

Candesartan Cilexetil Related Compound F

Pharmaceutical Secondary Standard; Certified Reference Material

Synonim(y):

(1-(Cyclohexyloxycarbonyloxy]ethyl 2-ethoxy-1-{[2′-(2-ethyl-2H-tetrazol-5-yl)-biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylate

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Do Państwa/SKUDostępnośćCena netto
20 mg
Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności
2910,00 zł

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C35H38N6O6
Masa cząsteczkowa:
638.71
NACRES:
NA.24
UNSPSC Code:
41116107

2910,00 zł


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Quality Segment

grade

certified reference material, pharmaceutical secondary standard

agency

traceable to USP 1087869

API family

candesartan

CofA

current certificate can be downloaded

packaging

pkg of 20 mg

application(s)

pharmaceutical small molecule

format

neat

storage temp.

2-8°C

General description

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.
Candesartan cilexetil is a selective antagonist to Angiotensin II receptors, that plays a crucial role in blood pressure regulation and sodium homeostasis, and is popularly used for the treatment of hypertension, diabetic nephropathy and congestive heart failure.

Application

Candesartan cilexetil may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by spectrophotometric and chromatographic 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.

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 LRAB4750 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
PHR2019PHR2018PHR2036
description

Pharmaceutical Secondary Standard; Certified Reference Material

description

Pharmaceutical Secondary Standard; Certified Reference Material

description

Pharmaceutical Secondary Standard; Certified Reference Material

description

Pharmaceutical Secondary Standard; Certified Reference Material

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical small molecule

application(s)

pharmaceutical

application(s)

pharmaceutical

format

neat

format

neat

format

neat

format

neat

Quality Level

300

Quality Level

300

Quality Level

300

Quality Level

300

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

grade

certified reference material, pharmaceutical secondary standard

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

packaging

pkg of 20 mg

packaging

pkg of 20 mg

packaging

pkg of 20 mg

packaging

pkg of 20 mg


Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



Wybierz jedną z najnowszych wersji:

Certyfikaty analizy (CoA)

Lot/Batch Number

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