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Details

Stereochemistry RACEMIC
Molecular Formula C6H13NO2
Molecular Weight 131.1729
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LEUCINE, DL-

SMILES

CC(C)CC(N)C(O)=O

InChI

InChIKey=ROHFNLRQFUQHCH-UHFFFAOYSA-N
InChI=1S/C6H13NO2/c1-4(2)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)

HIDE SMILES / InChI

Molecular Formula C6H13NO2
Molecular Weight 131.1729
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Non-ionic surfactant modified ligand exchange chromatography using copper (II) complex of N,N-dimethyl-L-phenylalanine as the chiral additive for enantioselective amino acids separation.
2010-03-17
Abstracts of the 2008 ISSOL Meeting. August 24-29, 2008. Florence, Italy.
2009-08
Highly sensitive detection of chiral amino acids by CE based on on-line stacking techniques.
2009-07
[Chemical constituents from Centipeda minima].
2009-06
Enantioselective lactate binding by chiral tripodal anion hosts derived from amino acids.
2009-04-21
Chemotactic tripeptides incorporating at position 2 alpha-aminoacid residues with unsaturated side chains.
2008-08
Oligopeptides and copeptides of homochiral sequence, via beta-sheets, from mixtures of racemic alpha-amino acids, in a one-pot reaction in water; relevance to biochirogenesis.
2008-07-09
Copper(II) 12-metallacrown-4 complexes of alpha-, beta- and gamma-aminohydroxamic acids: a comparative thermodynamic study in aqueous solution.
2008-05-28
Direct lung delivery of a dry powder formulation of DTPA with improved aerosolization properties: effect on lung and systemic decorporation of plutonium.
2007-03-12
Effect of polyamines and synthetic polyamine-analogues on the expression of antizyme (AtoC) and its regulatory genes.
2007-01-15
Homochiral oligopeptides via a lattice-controlled polymerisation in racemic crystals of valine N-carboxyanhydride suspended in aqueous solutions.
2007
3-Methylglutaconyl-CoA hydratase from Acinetobacter sp.
2006-05
Copolymerized polymeric surfactants: characterization and application in micellar electrokinetic chromatography.
2003-12
Synthesis, structure analysis, solution chemistry, and in vitro insulinomimetic activity of novel oxovanadium(IV) complexes with tripodal ligands containing an imidazole group derived from amino acids.
2003-11
Insulin is protein-anabolic in chronic renal failure patients.
2003-09
Viscosity behavior of some alpha-amino acids and their groups in water-sodium acetate mixtures.
2002-11-06
Liquid chromatographic resolution of N-acyl-alpha-amino acids as their anilide derivatives on a chiral stationary phase based on (S)-leucine.
2002-06
Asymmetric synthesis of alpha-branched primary amines on solid support via novel hydrazine resins.
2001-04-19
Cryo-bioorganic chemistry: freezing effect on stereoselection of L- and DL-leucine cooligomerization in aqueous solution.
2001-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:47:10 GMT 2025
Edited
by admin
on Mon Mar 31 18:47:10 GMT 2025
Record UNII
1QSS9D5DR6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LEUCINE, DL-
Systematic Name English
DL-LEUCINE
FCC  
Preferred Name English
(±)-2-AMINO-4-METHYLVALERIC ACID
Systematic Name English
DL-LEUCINE [FCC]
Common Name English
NSC-9252
Code English
Code System Code Type Description
CAS
328-39-2
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
PRIMARY
ECHA (EC/EINECS)
206-328-2
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
PRIMARY
CHEBI
25017
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
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FDA UNII
1QSS9D5DR6
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
PRIMARY
EVMPD
SUB20905
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
PRIMARY
PUBCHEM
857
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
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EPA CompTox
DTXSID00859050
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
PRIMARY
NSC
9252
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
PRIMARY
SMS_ID
100000087036
Created by admin on Mon Mar 31 18:47:10 GMT 2025 , Edited by admin on Mon Mar 31 18:47:10 GMT 2025
PRIMARY