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5α-Pregnan-11β,17α,21-triol-3,20-dione-1,2,4,5-D4 is a synthetically derived isotopically labeled research compound. It is characterized by its unique molecular structure, which features a pregnane core with three hydroxyl groups at the 11β, 17α, and 21 positions, and a dione group at the 3,20 positions. The presence of deuterium atoms at the 1,2,4,5 positions further distinguishes 5A-PREGNAN-11B,17A,21-TRIOL-3,20-DIONE-1,2,4,5-D4 from its non-labeled counterparts. 5A-PREGNAN-11B,17A,21-TRIOL-3,20-DIONE-1,2,4,5-D4 is primarily used for research purposes, particularly in the study of steroidal compounds and their biological effects.

252976-11-7

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252976-11-7 Usage

Uses

Used in Pharmaceutical Research:
5α-Pregnan-11β,17α,21-triol-3,20-dione-1,2,4,5-D4 is used as a research compound in pharmaceutical research for the investigation of its potential therapeutic effects and mechanisms of action. Its unique structure and isotopic labeling make it a valuable tool for studying the interactions of steroidal compounds with biological targets and their metabolic pathways.
Used in Steroid Hormone Studies:
In the field of endocrinology, 5α-Pregnan-11β,17α,21-triol-3,20-dione-1,2,4,5-D4 is used as a research compound to explore the role of steroid hormones in various physiological processes. Its isotopic labeling allows for the tracking of hormone metabolism and the elucidation of their effects on target tissues.
Used in Drug Metabolism and Pharmacokinetics:
5α-Pregnan-11β,17α,21-triol-3,20-dione-1,2,4,5-D4 is employed as a research tool in drug metabolism and pharmacokinetics studies. Its isotopic labeling enables researchers to monitor the compound's absorption, distribution, metabolism, and excretion, providing valuable insights into the pharmacological properties of steroidal compounds.
Used in Analytical Chemistry:
In analytical chemistry, 5α-Pregnan-11β,17α,21-triol-3,20-dione-1,2,4,5-D4 is utilized as a reference material for the development and validation of analytical methods. Its unique structure and isotopic labeling make it an ideal candidate for the calibration of instruments and the assessment of method performance in the analysis of steroidal compounds.
Used in Biochemical Research:
5α-Pregnan-11β,17α,21-triol-3,20-dione-1,2,4,5-D4 is used as a research compound in biochemical research to study the enzymatic reactions and pathways involved in the synthesis and metabolism of steroid hormones. Its isotopic labeling aids in the identification and quantification of reaction products and intermediates, contributing to a better understanding of the underlying biochemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 252976-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,9,7 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 252976-11:
(8*2)+(7*5)+(6*2)+(5*9)+(4*7)+(3*6)+(2*1)+(1*1)=157
157 % 10 = 7
So 252976-11-7 is a valid CAS Registry Number.

252976-11-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5A-PREGNAN-11B,17A,21-TRIOL-3,20-DIONE-1,2,4,5-D4

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:252976-11-7 SDS

252976-11-7Upstream product

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