3-Bodipy-propanoic Acid N-Phenethylspiperone Amide CAS 121086-10-0

Purity 97%+In StockPharmaceutical Standards
CAS No.121086-10-0
Molecular FormulaC45H48BF3N6O3
Molecular Weight788.71 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Bodipy-propanoic Acid N-Phenethylspiperone Amide CAS 121086-10-0 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 3-Bodipy-propanoic Acid N-Phenethylspiperone Amide.

3-Bodipy-propanoic Acid N-Phenethylspiperone Amide (CAS 121086-10-0) is a high-purity analytical reference standard with the molecular formula C45H48BF3N6O3 and a molecular weight of 788.71 g/mol.

3-Bodipy-propanoic Acid N-Phenethylspiperone Amide (C45H48BF3N6O3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, 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 3-Bodipy-propanoic Acid N-Phenethylspiperone Amide 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 FormulaC45H48BF3N6O3
Molecular Weight788.71 g/mol
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)23.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentF-containing
Nitrogen Atoms6

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