Dehydroisoandrosterone 3-acetate

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Chemical Name:Dehydroisoandrosterone 3-acetate
CAS.NO:853-23-6
Synonyms:
DEHYDROEPIANDROSTERONE-3-ACETATE
Dehydroepiandrosterone acetate
DHEAacetate(prasterone acetate)
DEHYDROISOANDROSTERONE ACETATE

Molecular Formula:C21H30O3
Molecular Weight:330.46100

Physical and Chemical Properties:
Density: 1.09 g / cm3
Boiling point: 434.8ºC at 760 mmHg
Melting point: 168-170ºC
Flash point: 188.1ºC
Refractive index: 1.54

Specification:
Appearance:White to almost white crystalline powder
Purity:≥98%
Loss on drying: ≤0.5%
Impurity: ≤0.5%

Packing:
 25kg  cardboard drum or according to customer specified requirements
Storage:Stored in a cool and dry well-closed container. Keep away from moisture and strong light/heat.
Application:Intermediates of Abiraterone CAS:154229-19-3
Intermediates of Abiraterone acetate CAS:154229-18-2

Dehydroisoandrosterone 3-acetate


Related News: “Administrative Measures for the Joint Review, Review and Approval of Raw Materials, Medicinal Auxiliaries and Pharmaceutical Packaging Materials and Pharmaceutical Preparations” (Consultation Draft) issued by the State Food and Drug Administration in December 2017. Supervision departments no longer accept applications for registration of APIs, pharmaceutical excipients, and packaging materials.1516-55-8 It does not require a production license for the drug substance, and can be produced in an ordinary chemical plant. As long as it reaches a certain level, it can be used for the synthesis of the drug substance.2-fluoro-5-nitropiridina CAS:456-24-6 With the structural upgrade of the pharmaceutical industry in developed countries, the transfer of related industrial chains has taken place globally, and it has also had a profound impact on Chinese pharmaceutical companies. nearN-Acetyl-L-Leucine With the structural upgrade of the pharmaceutical industry in developed countries, the transfer of related industrial chains has taken place globally, and it has also had a profound impact on Chinese pharmaceutical companies. nearWith the improvement of domestic GMP management level, the increase of process development capabilities and international certification experience, China has already possessed the conditions for developing characteristic APIs.

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