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Merck

PHR1540

Letrozole

Pharmaceutical Secondary Standard; Certified Reference Material

Sinonimo/i:

Letrozole, 4,4′-(1H-1,2,4-Triazol-1-ylmethylene)bisbenzonitrile

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1 G

127,00 €

127,00 €


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Informazioni su questo articolo

Formula empirica (notazione di Hill):
C17H11N5
Numero CAS:
Peso molecolare:
285.30
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
MDL number:

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Nome del prodotto

Letrozole, Pharmaceutical Secondary Standard; Certified Reference Material

format

neat

InChI

1S/C17H11N5/c18-9-13-1-5-15(6-2-13)17(22-12-20-11-21-22)16-7-3-14(10-19)4-8-16/h1-8,11-12,17H

SMILES string

N#CC(C=C1)=CC=C1C(N2C=NC=N2)C3=CC=C(C#N)C=C3

InChI key

HPJKCIUCZWXJDR-UHFFFAOYSA-N

grade

certified reference material
pharmaceutical secondary standard

agency

traceable to Ph. Eur. Y0000685
traceable to USP 1356971

API family

letrozole

CofA

current certificate can be downloaded

packaging

pkg of 1 g

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

pharmaceutical (small molecule)

storage temp.

2-30°C

Quality Level

Gene Information

human ... CYP19A1(1588)

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Questo articolo
L65451356971Y0000685
Letrozole Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1540

Letrozole

Letrozole ≥98% (HPLC)

Sigma-Aldrich

L6545

Letrozole

Letrozole United States Pharmacopeia (USP) Reference Standard

USP

1356971

Letrozole

Letrozole European Pharmacopoeia (EP) Reference Standard

Y0000685

Letrozole

application(s)

pharmaceutical (small molecule)

application(s)

-

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

-

technique(s)

-

technique(s)

-

format

neat

format

-

format

neat

format

neat

Quality Level

300

Quality Level

100

Quality Level

-

Quality Level

-

grade

certified reference material, pharmaceutical secondary standard

grade

-

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

storage temp.

2-30°C

storage temp.

2-8°C

storage temp.

-

storage temp.

2-8°C

Analysis Note

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

Application

Letrozole may be used as a pharmaceutical reference standard for the determination of the analyte in biological/environmental samples[1][2] and pharmaceutical formulations[3] 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.

Biochem/physiol Actions

Letrozole is a non-steroidal aromatase inhibitor.
Letrozole is a third generation nonsteroidal aromatase inhibitor. It is a competitive inhibitor of the aromatase enzyme system and thus inhibits the conversion of androgens to estrogens. Letrozole inhibits the aromatase enzyme by competitively binding to the heme of the cytochrome P450 subunit of the enzyme, resulting in a reduction of estrogen biosynthesis in all tissues.

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.
Letrozole is used for the treatment of breast cancer in hormone-dependent postmenopausal patients. The drug works by blocking the synthesis of estrogen, a causative agent for cancer.[1]

Other Notes

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.
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 LRAA4186 in the slot below. This is an example certificate only and may not be the lot that you receive.

pictograms

Health hazard

signalword

Warning

Hazard Classifications

Repr. 2 - STOT RE 2

Classe di stoccaggio

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Rapid quantitative analysis of letrozole, fluoxetine and their metabolites in biological and environmental samples by MEKC
Rodriguez?Flores, et al.
Electrophoresis, 30(4), 624-632 (2009)
Determination of letrozole in tablet formulations by reversed phase high performance liquid chromatography
Ganesh M, et al.
Tropical Journal of Pharmaceutical Research, 9(5), 505-510 (2010)
Rapid determination of letrozole, citalopram and their metabolites by high performance liquid chromatography-fluorescence detection in urine: Method validation and application to real samples
Rodriguez J, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 913, 12-18 (2013)
L Zhou et al.
Journal of neuroendocrinology, 26(7), 439-447 (2014-05-02)
During the oestrus cycle, varying spine synapse density correlates positively with varying local synthesis of oestradiol in the hippocampus. In this context, the roles of the oestrogen receptor (ER) subtypes ERα and β are not fully understood. In the present
Adina Dumitrescu et al.
Endocrinology, 155(12), 4774-4784 (2014-09-24)
We have previously shown that estrogen selectively suppresses growth of the fetal zone of the baboon fetal adrenal cortex, which produces the C19-steroid precursors, eg, dehydroepiandrosterone sulfate, which are aromatized to estrogen within the placenta. In the present study, we

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