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2812-28-4

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2812-28-4 Usage

Description

H-L-METHR-OH HCL, also known as hydroxylmethylnortestosterone, is a synthetic androgenic-anabolic steroid derived from nandrolone. It features a methyl group and a hydroxyl group added at the 17th position, enhancing its oral bioavailability and reducing liver toxicity potential. This chemical compound is primarily utilized in the development of new drugs and research studies within endocrinology and sports medicine.

Uses

Used in Pharmaceutical Development:
H-L-METHR-OH HCL is used as a pharmaceutical compound for the development of new drugs that aim to treat conditions related to hormonal imbalances and muscle wasting.
Used in Research Studies:
In the field of endocrinology, H-L-METHR-OH HCL is used as a research tool to study the effects of androgenic-anabolic steroids on the human body, particularly their impact on muscle growth, strength, and hormonal regulation.
Used in Sports Medicine:
H-L-METHR-OH HCL is utilized as a therapeutic agent in sports medicine for the treatment of conditions that involve muscle atrophy and weakness, such as osteoporosis, sarcopenia, and muscle dystrophy. Its anabolic properties promote muscle growth and strength, improving the physical performance of athletes.
Used in Anti-Aging Therapies:
H-L-METHR-OH HCL is employed as an anti-aging agent, targeting age-related muscle loss and hormonal decline. Its anabolic and androgenic effects help maintain muscle mass, strength, and overall physical fitness in older individuals.
Used in Hormone Replacement Therapy:
In the medical field, H-L-METHR-OH HCL is used as a hormone replacement therapy for individuals suffering from hormonal deficiencies, such as hypogonadism. It helps restore normal hormone levels, improving overall health and well-being.
Used in Bodybuilding and Performance Enhancement:
Although not recommended for non-medical use, H-L-METHR-OH HCL has been known to be utilized in bodybuilding and athletic performance enhancement due to its anabolic and androgenic properties. It increases muscle mass, strength, and endurance, providing a competitive edge in sports.

Check Digit Verification of cas no

The CAS Registry Mumber 2812-28-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2812-28:
(6*2)+(5*8)+(4*1)+(3*2)+(2*2)+(1*8)=74
74 % 10 = 4
So 2812-28-4 is a valid CAS Registry Number.

2812-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-3-hydroxy-2-(methylamino)butanoic acid

1.2 Other means of identification

Product number -
Other names N-Methylthreonine

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:2812-28-4 SDS

2812-28-4Downstream Products

2812-28-4Relevant articles and documents

Mirabamides E-H, HIV-inhibitory depsipeptides from the sponge Stelletta clavosa

Lu, Zhenyu,Van Wagoner, Ryan M.,Harper, Mary Kay,Baker, Heather L.,Hooper, John N. A.,Bewley, Carole A.,Ireland, Chris M.

experimental part, p. 185 - 193 (2011/04/26)

Four new depsipeptides, mirabamides E-H (1-4), and the known depsipeptide mirabamide C (5) have been isolated from the sponge Stelletta clavosa, collected from the Torres Strait. The planar structures were determined on the basis of extensive 1D and 2D NMR and HRESIMS. The absolute configurations were established by the advanced Marfey's method, NMR, and GC-MS. The four new compounds all showed strong inhibition of HIV-1 in a neutralization assay with IC50 values of 121, 62, 68, and 41 nM, respectively.

N-alkylation of amino acids during hydrogenolytic deprotection

Filira,Biondi,Gobbo,Rocchi

, p. 7463 - 7464 (2007/10/02)

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