6-[N-(6-MAleimidocaproyl)]caproic acid nhs CAS 1337538-62-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1337538-62-1
Molecular FormulaC20H27N3O7
Molecular Weight421.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-[N-(6-MAleimidocaproyl)]caproic acid nhs CAS 1337538-62-1 chemical structure

Description

CATO manufactures 6-[N-(6-MAleimidocaproyl)]caproic acid nhs 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.

CATO supplies 6-[N-(6-MAleimidocaproyl)]caproic acid nhs (CAS 1337538-62-1), a certified reference material (molecular formula C20H27N3O7, MW 421.44 g/mol) for analytical method development and quality control.

The molecular framework of 6-[N-(6-MAleimidocaproyl)]caproic acid nhs (C20H27N3O7) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

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.

Physical & Chemical Properties

Molecular FormulaC20H27N3O7
Molecular Weight421.44 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms3

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