.alpha.-Bromo-.gamma.-butyrolactone .alpha.-Bromobutyric acid, .gamma.-lactone .alpha.-Bromobutyrolactone 2(3H)-Furanone, 3-bromodihydro- 2-Bromo-.gamma.-butyrolactone 2-Bromo-4-butanolide 2-Bromobutyrolactone 3-Bromo-2-furanone 5061-21-2 NSC-56959 NSC56959 CAS 5061-21-2

Purity 97%+In StockPharmaceutical Standards
CAS No.5061-21-2
Molecular FormulaC4H5BrO2
Molecular Weight164.99 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

.alpha.-Bromo-.gamma.-butyrolactone
.alpha.-Bromobutyric acid, .gamma.-lactone
.alpha.-Bromobutyrolactone
2(3H)-Furanone, 3-bromodihydro-
2-Bromo-.gamma.-butyrolactone
2-Bromo-4-butanolide
2-Bromobutyrolactone
3-Bromo-2-furanone
5061-21-2
NSC-56959
NSC56959 CAS 5061-21-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 164.99 g/mol gives .alpha.-Bromo-.gamma.-butyrolactone .alpha.-Bromobutyric acid, .gamma.-lactone .alpha.-Bromobutyrolactone 2(3H)-Furanone, 3-bromodihydro- 2-Bromo-.gamma.-butyrolactone 2-Bromo-4-butanolide 2-Bromobutyrolactone 3-Bromo-2-furanone 5061-21-2 NSC-56959 NSC56959 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

.alpha.-Bromo-.gamma.-butyrolactone .alpha.-Bromobutyric acid, .gamma.-lactone .alpha.-Bromobutyrolactone 2(3H)-Furanone, 3-bromodihydro- 2-Bromo-.gamma.-butyrolactone 2-Bromo-4-butanolide 2-Bromobutyrolactone 3-Bromo-2-furanone 5061-21-2 NSC-56959 NSC56959 (CAS 5061-21-2), molecular formula C4H5BrO2 and molecular weight 164.99 g/mol, is a CATO reference standard with documented purity and traceability.

.alpha.-Bromo-.gamma.-butyrolactone .alpha.-Bromobutyric acid, .gamma.-lactone .alpha.-Bromobutyrolactone 2(3H)-Furanone, 3-bromodihydro- 2-Bromo-.gamma.-butyrolactone 2-Bromo-4-butanolide 2-Bromobutyrolactone 3-Bromo-2-furanone 5061-21-2 NSC-56959 NSC56959 (C4H5BrO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures .alpha.-Bromo-.gamma.-butyrolactone .alpha.-Bromobutyric acid, .gamma.-lactone .alpha.-Bromobutyrolactone 2(3H)-Furanone, 3-bromodihydro- 2-Bromo-.gamma.-butyrolactone 2-Bromo-4-butanolide 2-Bromobutyrolactone 3-Bromo-2-furanone 5061-21-2 NSC-56959 NSC56959 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC4H5BrO2
Molecular Weight164.99 g/mol
Purity97%+
StorageStore at 2-8°C, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityContains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)2.0
CAS Registry Year (est.)1958
Halogen ContentBr-containing

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