L-Glutamic acid diallyl ester (tosylate) CAS 20845-16-3

Purity 97%+In StockPharmaceutical Standards
CAS No.20845-16-3
Molecular FormulaC11H17NO4
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

L-Glutamic acid diallyl ester (tosylate) CAS 20845-16-3 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 L-Glutamic acid diallyl ester (tosylate) (CAS 20845-16-3), a certified reference material (molecular formula C11H17NO4C7H8O3S, MW 399.46 g/mol) for analytical method development and quality control.

L-Glutamic acid diallyl ester (tosylate) (C11H17NO4C7H8O3S) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), L-Glutamic acid diallyl ester (tosylate) meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H17NO4 C7H8O3S
Molecular Weight399.46 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1962
Nitrogen Atoms1
Sulfur Atoms1

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