1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid CAS 208772-41-2

Purity 97%+In StockPharmaceutical Standards
CAS No.208772-41-2
Molecular FormulaC14H17NO4
Molecular Weight263.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid CAS 208772-41-2 chemical structure

Description

CATO manufactures 1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid 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 1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid (CAS 208772-41-2), a certified reference material (molecular formula C14H17NO4, MW 263.29 g/mol) for analytical method development and quality control.

Structurally, 1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid (C14H17NO4) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 263.29 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

Physical & Chemical Properties

Molecular FormulaC14H17NO4
Molecular Weight263.29 g/mol
AppearanceOff-white to pale yellow crystalline powder
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; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2016
Nitrogen Atoms1

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