Skip to Content
Merck
All Photos(1)

Documents

61238

Sigma-Aldrich

(S)-γ-Valerolactone

≥97.5% (GC)

Synonym(s):

(5S)-4-Hydroxypentanoic acid lactone, (5S)-5-Methyloxolan-2-one, (S)-γ-Methyl-γ-butyrolactone, (S)-Dihydro-5-methyl-2(3H)-furanone, (S)-5-Methyl-2-oxotetrahydrofuran

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C5H8O2
CAS Number:
19041-15-7
Molecular Weight:
100.12
Beilstein:
3536337
MDL number:
MFCD01863132
UNSPSC Code:
12352204
PubChem Substance ID:
329759404

Assay

≥97.5% (GC)

form

liquid

optical purity

enantiomeric excess: ≥97.0% (GC)

storage temp.

2-8°C

SMILES string

C[C@H]1CCC(O1)=O

InChI

1S/C5H8O2/c1-4-2-3-5(6)7-4/h4H,2-3H2,1H3/t4-/m0/s1

InChI key

GAEKPEKOJKCEMS-BYPYZUCNSA-N

Looking for similar products? Visit Product Comparison Guide

Biochem/physiol Actions

Metabolite for urine analysis, metabolite of interest in pathways of biomass utilization.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Gorissen, H. J., et al.
Chirality, 4, 286-294 (1992)
Shinji Nakamura et al.
Journal of the American Chemical Society, 126(28), 8769-8776 (2004-07-15)
The mechanism of the optical resolution of gamma-valerolactone (VAL) enantiomers by enclathration in cholic acid (CA) channels was investigated. 13C cross-polarization magic-angle spinning spectra of CA/VAL inclusion compounds show four methyl 13C peaks of VAL with different intensities depending on
Identification of the metabolites of n-hexane, cyclohexane, and their isomers in men's urine.
L Perbellini et al.
Toxicology and applied pharmacology, 53(2), 220-229 (1980-04-01)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service