Benzyl 6-aminohexanoate 4-methylbenzenesulfonate CAS 5514-99-8

Purity 97%+In StockPharmaceutical Standards
CAS No.5514-99-8
Molecular FormulaC15H10ClF3N2O4
Molecular Weight374.70 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Benzyl 6-aminohexanoate 4-methylbenzenesulfonate CAS 5514-99-8 chemical structure

Description

Owing to a flavonoid core, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, Benzyl 6-aminohexanoate 4-methylbenzenesulfonate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 374.70 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies Benzyl 6-aminohexanoate 4-methylbenzenesulfonate (CAS 5514-99-8), a certified reference material (molecular formula C15H10ClF3N2O4, MW 374.70 g/mol) for analytical method development and quality control.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures Benzyl 6-aminohexanoate 4-methylbenzenesulfonate 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 FormulaC15H10ClF3N2O4
Molecular Weight374.70 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Halogen ContentF/Cl-containing
Nitrogen Atoms2

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