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6300-78-3

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6300-78-3 Usage

Description

(S)-2-AMINO-2-ETHYLHEXANOIC ACID, also known as leucine, is an essential amino acid that plays a vital role in protein synthesis, overall growth, and repair of the body. As one of the three branched-chain amino acids, it is commonly found in various food sources such as meat, dairy products, and legumes. Leucine is crucial for regulating blood sugar levels, aiding in tissue and bone healing, and providing energy for muscles during exercise. It has also been associated with improved cognitive function and the prevention of muscle loss during aging.

Uses

Used in Nutritional Supplements:
Leucine is used as a dietary supplement for athletes and individuals seeking to optimize muscle growth and overall physical performance. It supports protein synthesis, muscle recovery, and energy production during exercise.
Used in Healthcare:
Leucine is utilized in healthcare for its role in regulating blood sugar levels, contributing to the healing of tissues and bones, and preventing muscle loss during aging. It can be particularly beneficial for individuals with conditions that affect muscle mass and function.
Used in Sports Nutrition:
In the sports nutrition industry, leucine is used as an ingredient in various products designed to enhance athletic performance, muscle growth, and recovery. It is often combined with other branched-chain amino acids and nutrients to create comprehensive supplements for athletes.
Used in Functional Foods:
Leucine can be incorporated into functional foods and beverages, targeting consumers who are looking for health benefits beyond basic nutrition. These products may include protein shakes, meal replacement bars, and other supplements that promote muscle growth, recovery, and overall health.

Check Digit Verification of cas no

The CAS Registry Mumber 6300-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6300-78:
(6*6)+(5*3)+(4*0)+(3*0)+(2*7)+(1*8)=73
73 % 10 = 3
So 6300-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H17NO2/c1-3-5-6-8(9,4-2)7(10)11/h3-6,9H2,1-2H3,(H,10,11)

6300-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-AMINO-2-ETHYLHEXANOIC ACID

1.2 Other means of identification

Product number -
Other names DL-Norleucine,2-ethyl

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:6300-78-3 SDS

6300-78-3Relevant articles and documents

The first fully planar C5-conformation of homooligopeptides prepared from a chiral α-ethylated α,α-disubstituted amino acid: (S)-butylethylglycine (=(2S)-2-amino-2-ethylhexanoic acid)

Imawaka, Naoto,Tanaka, Masakazu,Suemune, Hiroshi

, p. 2823 - 2835 (2007/10/03)

An optically active α-ethylated α,α-disubstituted amino acid, (S)-butylethylglycine (=(2S)-2-amino-2-ethylhexanoic acid; (S)-Beg; (S)-2), was prepared starting from butyl ethyl ketone (1) by the Strecker method and enzymatic kinetic resolution of the racemic amino acid. Homooligopeptides containing (S)-Beg (up to hexapeptide) were synthesized by conventional solution methods. An ethyl ester was used for the protection at the C-terminus, and a trifluoroacetyl group was used for the N-terminus of the peptides. The structures of tri-and tetrapeptides 5 and 6 in the solid state were solved by X-ray crystallographic analysis, and were shown to have a bent planar C5-conformation (tripeptide) and a fully planar C5-conformation (tetrapeptide) (see Figs. 1 and 2, resp.). The IR and 1H-NMR spectra of hexapeptide 8 revealed that the dominant conformation in CDCl3 solution was also a fully planar C5-conformation. These results show for the first time that the preferred conformation of homopeptides containing a chiral α-ethylated α,α-disubstituted amino acid is a planar C5-conformation.

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