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82938-02-1

TESTOSTERONE (3,4-13C2) is a labeled form of testosterone, a principal hormone of the testes produced by the interstitial cells. It is a major circulating androgen that plays a crucial role in male sexual differentiation and development. The hormone is converted by 5α-reductase in androgen-dependent target tissues to 5α-dihydrotestosterone, which is required for normal male sexual differentiation. Additionally, it can be converted by aromatization to estradiol. TESTOSTERONE (3,4-13C2) is a controlled substance and is classified as an anabolic steroid and androgen.

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  • 82938-02-1 Structure

  • Basic information

    1. Product Name: TESTOSTERONE (3,4-13C2)
    2. Synonyms: TESTOSTERONE (3,4-13C2);(8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
    3. CAS NO:82938-02-1
    4. Molecular Formula: C19H28O2
    5. Molecular Weight: 290.44
    6. EINECS: N/A
    7. Product Categories: Intermediates & Fine Chemicals;Isotope Labelled Compounds;Pharmaceuticals;Steroids
    8. Mol File: 82938-02-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: TESTOSTERONE (3,4-13C2)(CAS DataBase Reference)
    10. NIST Chemistry Reference: TESTOSTERONE (3,4-13C2)(82938-02-1)
    11. EPA Substance Registry System: TESTOSTERONE (3,4-13C2)(82938-02-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 82938-02-1(Hazardous Substances Data)

82938-02-1 Usage

Uses

Used in Pharmaceutical Industry:
TESTOSTERONE (3,4-13C2) is used as a research tool for studying the metabolism, distribution, and effects of testosterone in the body. Its labeled form allows for easier tracking and analysis of the hormone's behavior in various biological systems.
Used in Sports and Fitness Industry:
TESTOSTERONE (3,4-13C2) is used as a controlled substance in the sports and fitness industry to monitor the use of anabolic steroids and ensure fair competition. The labeled form helps in detecting the presence of banned substances in athletes' samples.
Used in Hormone Replacement Therapy:
TESTOSTERONE (3,4-13C2) can be used as a hormone replacement therapy for individuals with testosterone deficiency. The labeled form allows for better monitoring of treatment efficacy and safety.
Used in Clinical Research:
TESTOSTERONE (3,4-13C2) is used in clinical research to study the effects of testosterone on various health conditions, such as osteoporosis, muscle wasting, and sexual dysfunction. The labeled form provides a more accurate assessment of the hormone's impact on these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 82938-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,3 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82938-02:
(7*8)+(6*2)+(5*9)+(4*3)+(3*8)+(2*0)+(1*2)=151
151 % 10 = 1
So 82938-02-1 is a valid CAS Registry Number.

82938-02-1Upstream product

82938-02-1Downstream Products

82938-02-1Relevant articles and documents

Synthesis of exemestane labelled with 13C

Fontana, Erminia,Pignatti, Alberto,Giribone, Danilo,Di Salle, Enrico

, p. 760 - 764 (2008/09/21)

The synthesis of exemestane (Aromasin), an irreversible steroidal aromatase inhibitor, specifically labelled with 13C is reported. The preparation of [13C3]exemestane was achieved according to an eight-step proc

SYNTHESIS OF 3,4-13C2 STEROIDS

Yuan, Sun-Shine

, p. 279 - 290 (2007/10/02)

A-ring enollactones 1a, 1b or 9 derived from 4-cholesten-3-one, testosterone benzoate or 3-oxo-4-estren-17β-yl benzoate were condensed with acetyl chloride to give intermediates 2a, 2b or 10. 2a and 2b were cyclized by acid or base to give 3,4-1

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