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Details

Stereochemistry ABSOLUTE
Molecular Formula C5H13NO
Molecular Weight 103.1628
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Valinol, L-

SMILES

CC(C)[C@H](N)CO

InChI

InChIKey=NWYYWIJOWOLJNR-RXMQYKEDSA-N
InChI=1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m1/s1

HIDE SMILES / InChI

Molecular Formula C5H13NO
Molecular Weight 103.1628
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
β-Amino alcohol selectors for enantioselective separation of amino acids by ligand-exchange capillary zone electrophoresis in a low molecular weight organogel.
2010-12
Synthesis of chiral β-aminoalcohol palladium complexes exhibiting cytotoxic properties.
2010-10-14
Absolute configurations and CD spectra of axially chiral biphenyls prepared in a facile manner by crystallization-induced configuration transformation.
2010-08
Amino acid derivatives from Lucilia sericata excretions/secretions may contribute to the beneficial effects of maggot therapy via increased angiogenesis.
2010-03
Synthesis of highly enantioenriched chiral alpha-aminoorganotins via diastereoselective ring opening of chiral N-(arenesulfonyl) 2-tributylstannyloxazolidines.
2009-08-21
Asymmetric synthesis of 8-aminoindolizidine from chiral 2-pyrroleimines.
2008-11-07
Highly enantioselective borane reduction of heteroaryl and heterocyclic ketoxime ethers catalyzed by novel spiroborate ester derived from diphenylvalinol: application to the synthesis of nicotine analogues.
2008-06-06
Vicinal amino alcohols as organocatalysts in asymmetric cross-aldol reaction of ketones: application in the synthesis of convolutamydine A.
2007-12-20
Peptaibiomics: microheterogeneity, dynamics, and sequences of trichobrachins, peptaibiotics from Trichoderma parceramosum Bissett (T. longibrachiatum Rifai).
2007-06
Polymeric alkenoxy amino acid surfactants: V. Comparison of carboxylate and sulfate head group polymeric surfactants for enantioseparation in MEKC.
2007-06
Molecular modeling of chiral-modified zeolite HY employed in enantioselective separation.
2007-06
Enantioseparation of phenylglycinol in chiral-modified zeolite HY: a molecular simulation study.
2007-06
Asymmetric route to pyridines bearing a highly functionalized 2-alkyl substituent by aziridine ring-opening reactions.
2007-05-11
Polymeric sulfated amino acid surfactants: a class of versatile chiral selectors for micellar electrokinetic chromatography (MEKC) and MEKC-MS.
2007-02-01
Gas-phase chiral separations by ion mobility spectrometry.
2006-12-15
Asymmetric synthesis of 2-(2-pyridyl)aziridines from 2-pyridineimines bearing stereogenic N-alkyl substituents and regioselective opening of the aziridine ring.
2006-12-08
Invariom-model refinement of L-valinol.
2006-11
The Bogorol family of antibiotics: template-based structure elucidation and a new approach to positioning enantiomeric pairs of amino acids.
2006-08-04
A cobalt(III)-salen complex with an axial substituent in the diamine backbone: stereoselective recognition of amino alcohols.
2005-12-07
Dinuclear complexes of chiral tetradentate pyridylimine ligands: diastereoselectivity, positive cooperativity, anion selectivity, ligand self-sorting based on chirality, and magnetism.
2004-01-26
Chiral bis(amino alcohol)oxalamide gelators-gelation properties and supramolecular organization: racemate versus pure enantiomer gelation.
2003-11-21
Identification of a novel system L amino acid transporter structurally distinct from heterodimeric amino acid transporters.
2003-10-31
A long-range chiral relay via tertiary amide group in asymmetric catalysis: new amino acid-derived N,P-ligands for copper-catalysed conjugate addition.
2003-08-07
Dietary low-dose sucrose modulation of IQ-induced genotoxicity in the colon and liver of Big Blue rats.
2003-06-19
Enantioselective synthesis of alpha-substituted ketones by asymmetric addition of chiral zinc enamides to 1-alkenes.
2003-05-28
A total synthesis of (-)-hemiasterlin using N-Bts methodology.
2001-11-02
Sequences of polypeptide antibiotics stilboflavins, natural peptaibol libraries of the mold Stilbella flavipes.
2001-08
Patents
Substance Class Chemical
Created
by admin
on Tue Apr 01 16:57:42 GMT 2025
Edited
by admin
on Tue Apr 01 16:57:42 GMT 2025
Record UNII
R54N4NJ3ZZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Valinol, L-
Common Name English
NSC-322922
Preferred Name English
[(S)-1-(Hydroxymethyl)-2-methylpropyl]amine
Systematic Name English
1-Butanol, 2-amino-3-methyl-, (2S)-
Systematic Name English
L-VALINOL
Systematic Name English
1-Butanol, 2-amino-3-methyl-, L-
Systematic Name English
(S)-Valinol
Common Name English
(2S)-2-Amino-3-methyl-1-butanol
Systematic Name English
(+)-Valinol
Common Name English
(+)-(S)-Valinol
Common Name English
(S)-(+)-2-Amino-3-methyl-1-butanol
Systematic Name English
Code System Code Type Description
CAS
2026-48-4
Created by admin on Tue Apr 01 16:57:42 GMT 2025 , Edited by admin on Tue Apr 01 16:57:42 GMT 2025
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EPA CompTox
DTXSID901318132
Created by admin on Tue Apr 01 16:57:42 GMT 2025 , Edited by admin on Tue Apr 01 16:57:42 GMT 2025
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PUBCHEM
640993
Created by admin on Tue Apr 01 16:57:42 GMT 2025 , Edited by admin on Tue Apr 01 16:57:42 GMT 2025
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DRUG BANK
DB04383
Created by admin on Tue Apr 01 16:57:42 GMT 2025 , Edited by admin on Tue Apr 01 16:57:42 GMT 2025
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FDA UNII
R54N4NJ3ZZ
Created by admin on Tue Apr 01 16:57:42 GMT 2025 , Edited by admin on Tue Apr 01 16:57:42 GMT 2025
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ECHA (EC/EINECS)
217-975-5
Created by admin on Tue Apr 01 16:57:42 GMT 2025 , Edited by admin on Tue Apr 01 16:57:42 GMT 2025
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NSC
322922
Created by admin on Tue Apr 01 16:57:42 GMT 2025 , Edited by admin on Tue Apr 01 16:57:42 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
SALT/SOLVATE -> PARENT