B103608

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B103608

Aldrich

 

γ-Butyrolactone

ReagentPlus®, ≥99%

Synonym:γ-Hydroxybutyric acid lactone, 4-Hydroxybutyric acid lactone, GBL
CAS Number:96-48-0
Linear Formula:C4H6O2
Molecular Weight:86.09
Beilstein Registry Number:105248
EC Number:202-509-5
MDL number:MFCD00005386
PubChem Substance ID:24891553

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Description

Packaging20 kg in VerSA-Flow™
 25, 500 g in glass btl
 3 kg in glass btl
 20 kg packaged in closed-head composite drums; 25 g, 500 g, 3 kg packaged in glass bottles
ApplicationFor the introduction of 3-carboxypropyl side chain.1 Used as a component of electrolyte solutions in batteries and capacitors.2
Biochem/physiol ActionsPrecursor of γ-hydroxybutyric acid (GHB). It blocks dopamine release by blocking impulse flow in dopaminergic neurons. Pretreatment with γ-butyrolactone allows detection of autoreceptor-induced dopamine release.
Legal InformationReagentPlus is a registered trademark of Sigma-Aldrich Biotechnology LP and Sigma-Aldrich Co.

Properties

gradeReagentPlus®
vapor density3 (vs air)
vapor pressure1.5 mmHg ( 20 °C)
assay≥99%
autoignition temp.851 °F
expl. lim.16 %
refractive indexn20/D 1.436(lit.)
bp204-205 °C(lit.)
mp−45 °C(lit.)
density1.12 g/mL at 25 °C(lit.)

Safety

Personal Protective EquipmentEyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Hazard CodesXn
Risk Statements22-36
Safety Statements26
WGK Germany1
RTECSLU3500000
UEL16.00%(V)
LEL1.40%(V)
Flash Point(F)208.4 °F
Flash Point(C)98 °C

References

Cited Reference1. J. Med. Chem. 34, 267, (1991) Abstract
 2. J. Power Sources 43, 195, (1993)
referenceWalters, J.R., and Roth, R.H., Dopaminergic neurons: drup-induced antagonism of the increase in tyrosine hydroxylase activity produced by cessation of impulse flow. J. Pharmacol. Exp. Ther. 191, 82-91, (1974)
 Ohkawa, S., et al., Dual inhibitors of thromboxane A2 synthase and 5-lipoxygenase with scavenging activity of active oxygen species. Synthesis of a novel series of (3-pyridylmethyl)benzoquinone derivatives. J. Med. Chem. 34, 267-276, (1991)
 Koeltzow, T.E., Alterations in dopamine release but not dopamine autoreceptor function in dopamine D3 receptor mutant mice. J. Neurosci. 18, 2231, (1998)
MerckMerck 13,1596
BeilsteinBeil. 17,V,9,7
FieserFieser 1,101
 Aldrich MSDS 1, 337:A / Arctander, 552 / Corp MSDS 1 (1), 656:A / FT-IR 2 (1), 1174:A / FT-IR 1 (1), 697:D / FT-NMR 1 (1), 1127:A / Fenaroli, 99 / IR-Spectra (2), 360:H / IR-Spectra (3), 407:F / NMR-Reference 2 (1), 590:C / RegBook 52 (1), 803:J / RegBook 1 (1), 803:J / Sax 6, 549 / Sigma FT-IR 1 (2), 623:A / Structure Index 1, 125:D:6 / Vapor Phase 3, 749:A