Autoinducing Peptide I trifluoroacetate salt CAS 200010-29-3

Purity 97%+In StockPharmaceutical Standards
CAS No.200010-29-3
Molecular FormulaC43H60N8O13S2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Autoinducing Peptide I trifluoroacetate salt CAS 200010-29-3 chemical structure

Description

The molecular framework of Autoinducing Peptide I trifluoroacetate salt (C43H60N8O13S2C2HF3O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. 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).

CATO supplies Autoinducing Peptide I trifluoroacetate salt (CAS 200010-29-3), a certified reference material (molecular formula C43H60N8O13S2C2HF3O2, MW 1075.14 g/mol) for analytical method development and quality control.

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

As a certified reference material (CRM), Autoinducing Peptide I trifluoroacetate salt meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC43H60N8O13S2 C2HF3O2
Molecular Weight1075.14 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)18.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2014
Halogen ContentF-containing
Nitrogen Atoms8
Sulfur Atoms2

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