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2-amino-5-hydroxy-pentanoic acid, also known as 5-hydroxy-L-lysine, is a naturally occurring amino acid derived from L-lysine. It plays a vital role in the biosynthesis of carnitine, which is essential for the transport of fatty acids into the mitochondria for energy production.
Used in Pharmaceutical Industry:
2-amino-5-hydroxy-pentanoic acid is used as an active pharmaceutical ingredient for its potential health benefits, including supporting cardiovascular health and promoting energy metabolism.
Used in Dietary Supplements:
2-amino-5-hydroxy-pentanoic acid is used as a dietary supplement to provide the essential amino acid and support overall health and well-being.
Used in Food Industry:
2-amino-5-hydroxy-pentanoic acid is found in protein-rich foods such as meat, dairy, and legumes, contributing to their nutritional value.

6152-89-2

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6152-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6152-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,5 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6152-89:
(6*6)+(5*1)+(4*5)+(3*2)+(2*8)+(1*9)=92
92 % 10 = 2
So 6152-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO3/c6-4(5(8)9)2-1-3-7/h4,7H,1-3,6H2,(H,8,9)

6152-89-2SDS

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 2-amino-5-hydroxy-pentanoic acid

1.2 Other means of identification

Product number -
Other names (S)-2-amino-5-hydroxy-valeric acid

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:6152-89-2 SDS

6152-89-2Relevant academic research and scientific papers

Drought stress increases the production of 5-hydroxynorvaline in two C4 grasses

Carmo-Silva, Ana E.,Keys, Alfred J.,Beale, Michael H.,Ward, Jane L.,Baker, John M.,Hawkins, Nathaniel D.,Arrabaca, Maria Celeste,Parry, Martin A.J.

experimental part, p. 664 - 671 (2010/02/17)

Plants produce various compounds in response to water deficit. Here, the presence and identification of a drought-inducible non-protein amino acid in the leaves of two C4 grasses is first reported. The soluble amino acids extracted from the lea

Reactivite du nitrite de sodium. V. Action sur les amino-acides, peptides et proteines

Gouesnard, Jean-Paul

, p. 88 - 94 (2007/10/02)

The action of sodium nitrite on various amino-acids was re-examined in conditions approximating to a biological medium. 13C-NMR provides evidence of the existence of intramolecular ring closures and the formation of 5-membered rings with ornithine, citrulline and arginine.The reaction of cystine shows the opening of the sulphur bridges, whereas cysteine leads to the formation of carboxy-thiiran and 3-sulpho-lactic acid.The hydrolysis of the amide bonds of asparagine and glutamine is complete whereas the peptides studied - carnosine and aspartam - do not undergo hydrolysis of the peptide linkage.However, the first deamination of glutathion (γ-Glu-Cys-Gly) induces the peptide link to be broken and a cyclization with the formation of lactone to occur.A second deamination takes place on the cysteinyl residue released and allows the formation of a thiiran by intramolecular cyclization with the thiol group.The formation of thiiran was also observed with oxidized glutathion which has an S-S bridge.Finally, the formation of nitrosamines was detected by 15N-NMR during the reaction of sodium nitrite with two commercial products available to the general public.

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