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18,20-cyclo-20,21-dihydroxy-4-pregnen-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10385-97-4

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10385-97-4 Usage

Chemical class

Steroidal compound

Role in fish reproduction

Crucial in reproductive processes

Hormone type

Progestin hormone

Functions

Involved in oocyte maturation and ovulation in female fish

Synthesis location

Synthesized in the gonads

Action on ovaries

Stimulates final maturation and release of eggs

Reproductive cycle regulation

Plays a role in regulating the reproductive cycle, particularly during the breeding season

Potential applications

Studied for use in aquaculture and as a tool for controlling fish reproduction
These properties and specific content provide a comprehensive overview of 18,20-cyclo-20,21-dihydroxy-4-pregnen-3-one and its significance in fish reproduction and potential applications in aquaculture.

Check Digit Verification of cas no

The CAS Registry Mumber 10385-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,8 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10385-97:
(7*1)+(6*0)+(5*3)+(4*8)+(3*5)+(2*9)+(1*7)=94
94 % 10 = 4
So 10385-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H30O4/c1-19-8-6-14(23)10-13(19)2-3-15-16(19)7-9-20-12-25-21(24,11-22)18(20)5-4-17(15)20/h10,15-18,22,24H,2-9,11-12H2,1H3/t15-,16+,17+,18?,19+,20?,21?/m1/s1

10385-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 18-Hydroxy-11-desoxy-corticosteron-cyclisches Halbacetal

1.2 Other means of identification

Product number -
Other names 18-Hydroxy-11-deoxycorticosteron

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:10385-97-4 SDS

10385-97-4Downstream Products

10385-97-4Relevant academic research and scientific papers

Differences between adrenal adenoma causing primary aldosteronism and other adrenal tissues in the incorporation of labeled steroid precursors into their products

Usa,Ganguly,Weinberger

, p. 531 - 545 (2007/10/02)

The incorporation and conversion of several labeled steroid precursors into their products were examined in slices of adrenal tissue from two patients with primary aldosteronism and compared with that in 'normal' adrenal tissue and adrenal tissues from a patient with Cushing's syndrome. The products of the incorporation were separated by Sephadex LH-20 column chromatography. The major products of conversion in the adenomatous tissue of primary aldosteronism were 18-hydroxycorticosterone and lesser amounts of aldosterone. Smaller amounts of 18-hydroxycorticosterone were isolated from all other adrenal tissues studied. No aldosterone could be recovered after incubating any of the adrenal tissue studied with labeled 18-hydroxy-11-deoxycorticosterone or 18-hydroxycorticosterone as precursor steroid. These in vitro results seem to suggest that there is increased 18-hydroxylation in the adenoma of primary aldosteronism compared with other tissues and that relatively more 18-hydroxycorticosterone is produced in such tissue than aldosterone.

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