Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)pent-4-ynoate CAS 63039-49-6

Purity 97%+In StockPharmaceutical Standards
CAS No.63039-49-6
Molecular FormulaC10H15NO4
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)pent-4-ynoate CAS 63039-49-6 chemical structure

Description

As a certified reference material (CRM), Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)pent-4-ynoate 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.

Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)pent-4-ynoate (CAS 63039-49-6), molecular formula C10H15NO4C12H23N and molecular weight 394.56 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, Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)pent-4-ynoate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 394.56 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 FormulaC10H15NO4 C12H23N
Molecular Weight394.56 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1975
Nitrogen Atoms2

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Why CATO?