Palmitoyl Tripeptide-1 HCl CAS 2757690-14-3

Purity >95%In StockPharmaceutical Standards
CAS No.2757690-14-3
Molecular FormulaC30H54N6O5
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Palmitoyl Tripeptide-1 HCl CAS 2757690-14-3 chemical structure

Description

The occurrence of Palmitoyl Tripeptide-1 HCl is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

Palmitoyl Tripeptide-1 HCl (CAS 2757690-14-3), molecular formula C30H54N6O5HCl and molecular weight 615.26 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, Palmitoyl Tripeptide-1 HCl is typically off-white to pale yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 615.26 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

As a certified reference material (CRM), Palmitoyl Tripeptide-1 HCl 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 FormulaC30H54N6O5 HCl
Molecular Weight615.26 g/mol
Purity>95%
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2002
Halogen ContentCl-containing
Nitrogen Atoms6

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Why CATO?