Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH CAS 141743-15-9

Purity >95%In StockPharmaceutical Standards
CAS No.141743-15-9
Molecular FormulaC24H28N2O6
Molecular Weight440.49 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH CAS 141743-15-9 chemical structure

Description

The occurrence of Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH is closely related to a flavonoid core, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH (CAS 141743-15-9), a certified reference material (molecular formula C24H28N2O6, MW 440.49 g/mol) for analytical method development and quality control.

Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH (C24H28N2O6) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 Fmoc-N-(N-β-Boc-aminoethyl)-Gly-OH 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 FormulaC24H28N2O6
Molecular Weight440.49 g/mol
AppearancePale yellow to yellow crystalline powder
Purity>95%
StorageStore in a cool place (≤25°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
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997
Nitrogen Atoms2

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