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H-BETA-ALA-ILE-OH, also known as beta-alanyl-L-isoleucine, is a dipeptide chemical compound consisting of beta-alanine, alanine, isoleucine, and a hydroxyl group. It is formed by the connection of two amino acids, beta-alanine and isoleucine, through a peptide bond. Beta-alanine is a non-proteinogenic amino acid that plays a crucial role in the synthesis of carnosine, a dipeptide abundant in muscle tissue. Isoleucine is an essential amino acid that contributes to protein synthesis and energy production. The hydroxyl group, containing an oxygen atom bonded to a hydrogen atom, is a functional group that influences the structure and function of organic compounds. H-BETA-ALA-ILE-OH may have potential applications in sports nutrition and muscle health due to its amino acid composition and molecular structure.

29727-65-9

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29727-65-9 Usage

Uses

Used in Sports Nutrition Industry:
H-BETA-ALA-ILE-OH is used as a dietary supplement for enhancing muscle carnosine synthesis. The presence of beta-alanine in the compound contributes to the production of carnosine, which helps buffer lactic acid in muscles during high-intensity exercise, thereby improving athletic performance and reducing muscle fatigue.
Used in Muscle Health Applications:
H-BETA-ALA-ILE-OH is used as a muscle health promoter for its potential to increase carnosine levels in muscle tissue. The elevated carnosine content may help protect muscles from damage, reduce inflammation, and support muscle recovery after strenuous exercise.
Used in Pharmaceutical Industry:
H-BETA-ALA-ILE-OH may be used as a therapeutic agent for muscle-related disorders. Its amino acid composition and molecular structure could potentially be utilized in the development of drugs targeting muscle diseases or conditions that benefit from enhanced muscle health and function.

Check Digit Verification of cas no

The CAS Registry Mumber 29727-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,7,2 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29727-65:
(7*2)+(6*9)+(5*7)+(4*2)+(3*7)+(2*6)+(1*5)=149
149 % 10 = 9
So 29727-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H18N2O3/c1-4-5(2)7(9(13)14)11-8(12)6(3)10/h5-7H,4,10H2,1-3H3,(H,11,12)(H,13,14)/t5?,6-,7-/m0/s1

29727-65-9SDS

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 H-β-ALA-ILE-OH

1.2 Other means of identification

Product number -
Other names H-L-Ala-L-Ile-OH

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:29727-65-9 SDS

29727-65-9Downstream Products

29727-65-9Relevant academic research and scientific papers

DIPEPTIDE-CONTAINING COMPOSITION FOR ORAL ADMINISTRATION

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Page/Page column 6, (2008/12/06)

The present invention provides a composition for oral administration, which comprises at least one kind of dipeptide represented by the formula: ????????X-Y (wherein X represents alanyl, glycyl, arginyl, seryl, α-aspartyl or α-glutamyl, and Y represents valine, leucine or isoleucine), with an object of providing a composition for oral administration which is excellent in nutrition, pharmacological effect and gustation and comprises at least one kind selected from valine, leucine and isoleucine, or providing a composition for oral administration which is excellent in processing characteristics such as solubility and tableting property and comprises at least one kind selected from valine, leucine and isoleucine.

Deprotection and cleavage of peptides bound to Merrifield resin by stable dimethyl ether-poly(hydrogen fluoride) (DMEPHF) complex, a new and convenient reagent for peptide chemistry

Toeroek, Bela,Busci, Imre,Prakash, G. K. Surya,Olah, George A.

, p. 2882 - 2883 (2007/10/03)

The newly developed stable DMEPHF (1/15) complex was found to be a highly effective reagent for the cleavage of peptides from Merrifield resins; ease of handling and its simple, complete removal from the reaction mixture make the reagent system a very useful HF equivalent for applications in solid-phase peptide synthesis.

ASYMMETRIC TRANSFORMATION OF AMINO ACIDS IN N-SALICYLIDENE AMINO ACYL-L-ISOLEUCINATOCOPPER(II)

Harada, Kaoru,Shiono, Katsuji,Nomoto, Shinya

, p. 1271 - 1274 (2007/10/02)

A new asymmetric transformation of amino acids was described.Thus, when N-salicylidene-D-alanyl-, D-phenylalanyl-, or D-phenyl-glycyl-L-isoleucinatocopper(II) was incubated at pH 8.5 and 80 deg C, the resulting mixture at equilibrium contained a complex of L-L-dipeptide in the contents of 63-76percent.The epimerization of dipeptides is based on the enhanced activity of N-terminal amino acids through complex formation.

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