Letrozole CAS:11280...

Letrozole CAS:112809-51-5

Letrozole CAS:112809-51-5

Min.Order / FOB Price:Get Latest Price

1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,D/A,D/P,T/T,,MoneyGram,Other

Keywords

Letrozole CAS:112809-51-5 Letrozole powder High quality with competitive price Letrozole

Quick Details

  • Appearance:White to yellowish, crystalline powder
  • Application:A nonsteroidal aromatase inhibitor structurally related to Fadrozole. Antineoplastic
  • PackAge:1kg/tin or per customer's requirement
  • ProductionCapacity:1000|Kilogram|Month
  • Storage:
  • Transportation:room temperature

Superiority:

1) Specialized in pharmaceutical industry since from 1987

2) ISO 9001:2015 & SGS audited supplier 

3) Accept better payment terms : T.T 30-60 days.on the basic of pass SINOSURE credit investigation.

5) We have warehouse in USA with quickly shipment .

6) We can do different terms of FOB ,CIF/CIP ,DDP ...

Details:

Company Information

Sinoway Industrial co., ltd. was established in 1987 in Xiamen, China, and now has been a leading group specialized in research, development, custom manufacturing and trading of pharmaceutical intermediates, APIs, health and food supplements, cosmetic raw materials, herbal extracts, polypeptides and prostaglandin derivatives, etc..

Product Information

Product name

Letrozole

Molecular Formula

C17H11N5

Molecular Weight

285.3

CAS No.

112809-51-5

Quality Standard

USP32, medical grade

Appearance

White powder

 

COA of Letrozole

Items

Specification

Appearance

White to yellowish, crystalline powder

Identification

A.IR spectrum of sample should be identical to that of Reference Standard;

The retention time of major peak in the chromatogram of the Assay preparation should correspond to that in the chromatogram of Standard preparation, as obtained in the Assay.

Showing the white precipitate reaction.

Water

Not more than 0.3%

Residue on Ignition

Not more than 0.1%

Heavy Metals

Not more than 0.001%

 

Related Compounds

Compound A: Not more than 0.1%

4,4’,4”-methylidenetrisbenzonitrile: Not more than 0.2%

Any other impurity: Not more than 0.1%

All other impurities: Not more than 0.3%

Residual Sovents

Ethanol: Not more than 3000ppm

Ethyl acetate: Not more than 2000ppm

DMF: Not more than 880ppm

Microbe Limit

Bacteria: Not more than 200/g

Mold and yeast: Not more than 50/g

Escherichia coli: should be absent

Assay(anhydrous)

98.0% to 102.0% of Cl7H11N5 on dried basis

Packaging and Storage

Preserve in tight containers at controlled room temperature.

Conclusion

Conforms to the USP32.

 

Usage

Function of Letrozole
Letrozole is a new generation of highly selective aromatase inhibitors. It is a synthetic benztriazole derivative. By inhibiting aromatase, estrogen levels are reduced, thereby eliminating the stimulating effect of estrogen on tumor growth. The activity in the body is 150-250 times stronger than that of the first generation aromatase inhibitor amuromet. Because of its high selectivity, it does not affect glucocorticoids, mineralocorticoids, and thyroid function. Large doses have no inhibitory effect on the secretion of adrenal corticosteroids, so it has a high therapeutic index. Various preclinical studies have shown that letrozole has no potential toxicity, mutagenicity and carcinogenic effects on various systems and target organs in the whole body, and has less toxic and side effects, and is well tolerated. Compared with estrogen drugs, the anti-tumor effect is stronger. It is suitable for the treatment of postmenopausal patients with advanced breast cancer who are not responding to anti-estrogen therapy and early treatment of breast cancer.

In December 2005, the British drug and health product regulatory agency approved Letrozole (Fron) produced by Novartis of Switzerland to be used in the treatment of breast cancer patients, allowing it to be used in surgically treated, early menopausal hormone-positive mammary glands Cancer patients. This is the second aromatase inhibitor approved following the approval of AstraZeneca ’s Rainin in June 2005. Both drugs have shown in clinical trials that they can better prevent the risk of breast cancer recurrence compared to current standard tamoxifen treatment.

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