1-3-4-6-Tetra-O-acetyl-2-O-nonafluorobutane-sulfonyl-β-D-mannopyranose CAS 480438-48-0

Purity 97%+In StockPharmaceutical Standards
CAS No.480438-48-0
Molecular FormulaC18H19F9O12S
Molecular Weight630.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-3-4-6-Tetra-O-acetyl-2-O-nonafluorobutane-sulfonyl-β-D-mannopyranose CAS 480438-48-0 chemical structure

Description

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

CATO supplies 1-3-4-6-Tetra-O-acetyl-2-O-nonafluorobutane-sulfonyl-β-D-mannopyranose (CAS 480438-48-0), a certified reference material (molecular formula C18H19F9O12S, MW 630.39 g/mol) for analytical method development and quality control.

Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system, 1-3-4-6-Tetra-O-acetyl-2-O-nonafluorobutane-sulfonyl-β-D-mannopyranose is typically off-white to pale yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 630.39 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO manufactures 1-3-4-6-Tetra-O-acetyl-2-O-nonafluorobutane-sulfonyl-β-D-mannopyranose 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 FormulaC18H19F9O12S
Molecular Weight630.39 g/mol
Purity97%+
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Sulfur Atoms1

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