Tert-butyl 6-(aminomethyl)-1,1-dimethylisoindoline-2-carboxylate CAS 2227204-84-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2227204-84-2
Molecular FormulaC16H24N2O2
Molecular Weight276.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 6-(aminomethyl)-1,1-dimethylisoindoline-2-carboxylate CAS 2227204-84-2 chemical structure

Description

Tert-butyl 6-(aminomethyl)-1,1-dimethylisoindoline-2-carboxylate (C16H24N2O2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, 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).

Tert-butyl 6-(aminomethyl)-1,1-dimethylisoindoline-2-carboxylate (CAS 2227204-84-2), molecular formula C16H24N2O2 and molecular weight 276.37 g/mol, is a CATO reference standard with documented purity and traceability.

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 Tert-butyl 6-(aminomethyl)-1,1-dimethylisoindoline-2-carboxylate 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 FormulaC16H24N2O2
Molecular Weight276.37 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 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Nitrogen Atoms2

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