Home Other Building Blocks Gamma-valerolactone

Gamma-valerolactone

CAS No.:
108-29-2
Catalog Number:
AG0034YQ
Molecular Formula:
C5H8O2
Molecular Weight:
100.1158
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$25
- +
100g
98%
In Stock USA
United States
$63
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG0034YQ
Chemical Name:
Gamma-valerolactone
CAS Number:
108-29-2
Molecular Formula:
C5H8O2
Molecular Weight:
100.1158
MDL Number:
MFCD00005400
IUPAC Name:
5-methyloxolan-2-one
InChI:
InChI=1S/C5H8O2/c1-4-2-3-5(6)7-4/h4H,2-3H2,1H3
InChI Key:
GAEKPEKOJKCEMS-UHFFFAOYSA-N
SMILES:
CC1CCC(=O)O1
EC Number:
203-569-5
NSC Number:
33700
FEMA Number:
3103
UN Number:
1224
Properties
Complexity:
88.1  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
100.052g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
100.117g/mol
Monoisotopic Mass:
100.052g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
26.3A^2
Undefined Atom Stereocenter Count:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
0.6  
Literature
Title Journal
Development of heterogeneous catalysts for the conversion of levulinic acid to γ-valerolactone. ChemSusChem 20120901
Gamma butyrolactone (GBL) and gamma valerolactone (GVL): similarities and differences in their effects on the acoustic startle reflex and the conditioned enhancement of startle in the rat. Pharmacology, biochemistry, and behavior 20120601
Production of aromatic hydrocarbons through catalytic pyrolysis of γ-valerolactone from biomass. Bioresource technology 20120601
5- and 6-membered (thio)lactones are prodrug type carbonic anhydrase inhibitors. Bioorganic & medicinal chemistry letters 20120101
Conversion of biomass-derived levulinate and formate esters into γ-valerolactone over supported gold catalysts. ChemSusChem 20111216
Liquid-phase catalytic transfer hydrogenation and cyclization of levulinic acid and its esters to γ-valerolactone over metal oxide catalysts. Chemical communications (Cambridge, England) 20111128
Selective homogeneous hydrogenation of biogenic carboxylic acids with [Ru(TriPhos)H]+: a mechanistic study. Journal of the American Chemical Society 20110914
Hydrogen-independent reductive transformation of carbohydrate biomass into γ-valerolactone and pyrrolidone derivatives with supported gold catalysts. Angewandte Chemie (International ed. in English) 20110816
Comparison of fermented soybean paste (Doenjang) prepared by different methods based on profiling of volatile compounds. Journal of food science 20110401
Reactive extraction of levulinate esters and conversion to γ-valerolactone for production of liquid fuels. ChemSusChem 20110321
Simultaneous determination of γ-Hydroxybutyrate (GHB) and its analogues (GBL, 1.4-BD, GVL) in whole blood and urine by liquid chromatography coupled to tandem mass spectrometry. Journal of analytical toxicology 20110101
Antioxidative activity of microbial metabolites of (-)-epigallocatechin gallate produced in rat intestines. Bioscience, biotechnology, and biochemistry 20110101
γ-Valerolactone ring-opening and decarboxylation over SiO2/Al2O3 in the presence of water. Langmuir : the ACS journal of surfaces and colloids 20101102
Conversion of levulinic acid and formic acid into γ-valerolactone over heterogeneous catalysts. ChemSusChem 20101025
Chemistry. Connecting biomass and petroleum processing with a chemical bridge. Science (New York, N.Y.) 20100730
Absolute configuration of isoeichlerialactone. Acta crystallographica. Section E, Structure reports online 20100401
Integrated catalytic conversion of gamma-valerolactone to liquid alkenes for transportation fuels. Science (New York, N.Y.) 20100226
A methodology to estimate concentration profiles from two-dimensional covariance spectroscopy applied to kinetic data. Applied spectroscopy 20100201
Bioavailability and catabolism of green tea flavan-3-ols in humans. Nutrition (Burbank, Los Angeles County, Calif.) 20100101
Palladium-catalyzed decarboxylative [4 + 3] cyclization of gamma-methylidene-delta-valerolactones with 1,1-dicyanocyclopropanes. Organic letters 20091217
Characterization of two lactones in liquid phase: an experimental and computational approach. Physical chemistry chemical physics : PCCP 20090814
MCR-ALS for sequential estimation of FTIR-ATR spectra to resolve a curing process using global phase angle convergence criterion. Analytica chimica acta 20090529
Catalytic conversion of biomass-derived carbohydrates into gamma-valerolactone without using an external H2 supply. Angewandte Chemie (International ed. in English) 20090101
Block copolymers for drug solubilisation: relative hydrophobicities of polyether and polyester micelle-core-forming blocks. International journal of pharmaceutics 20071210
Maximising opportunities in supercritical chemistry: the continuous conversion of levulinic acid to gamma-valerolactone in CO(2). Chemical communications (Cambridge, England) 20071128
Towards 'bio-based' Nylon: conversion of gamma-valerolactone to methyl pentenoate under catalytic distillation conditions. Chemical communications (Cambridge, England) 20070907
Gamma-hydroxybutyrate concentrations in the blood of impaired drivers, users of illicit drugs, and medical examiner cases. Journal of analytical toxicology 20070101
'Ionic carbenes': synthesis, structural characterization, and reactivity of rare-Earth metal methylidene complexes. Journal of the American Chemical Society 20060726
Difference in the volatile composition of pine-mushrooms (Tricholoma matsutake Sing.) according to their grades. Journal of agricultural and food chemistry 20060628
Predictive three-dimensional quantitative structure-activity relationship of cytochrome P450 1A2 inhibitors. Journal of medicinal chemistry 20050602
A theoretical study on the origin of pi-facial stereoselectivity in the alkylation of enolates derived from 4-substituted gamma-butyrolactones. Journal of the American Chemical Society 20050323
Sequential arrangement of gamma-valerolactone enantiomers enclathrated in cholic acid channels as studied by 13C solid-state NMR: elucidation of the optical resolution mechanism. Journal of the American Chemical Society 20040721
Phenol and lactone receptors in the distal sensilla of the Haller's organ in Ixodes ricinus ticks and their possible role in host perception. Experimental & applied acarology 20040101
Biosynthesis and local sequence specific degradation of poly(3-hydroxyvalerate-co-4-hydroxybutyrate) in Hydrogenophaga pseudoflava. Biomacromolecules 20030101
Clinical pharmacokinetics of antioxidants and their impact on systemic oxidative stress. Clinical pharmacokinetics 20030101
Versatile 8-oxabicyclo[3.2.1]oct-6-en-3-one: stereoselective methodology for generating C-glycosides, delta-valerolactones, and polyacetate segments. Organic letters 20010125
Properties