1,3-Di-O-tert-butyldimethylsilyl Paricalcitol 18-Aldehyde CAS 1257126-71-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1257126-71-8
Molecular FormulaC33H60O3Si2
Molecular Weight561.00 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,3-Di-O-tert-butyldimethylsilyl Paricalcitol 18-Aldehyde CAS 1257126-71-8 chemical structure

Description

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

1,3-Di-O-tert-butyldimethylsilyl Paricalcitol 18-Aldehyde (CAS 1257126-71-8) is a high-purity analytical reference standard with the molecular formula C33H60O3Si2 and a molecular weight of 561.00 g/mol.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system, 1,3-Di-O-tert-butyldimethylsilyl Paricalcitol 18-Aldehyde is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 561.00 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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).

As a certified reference material (CRM), 1,3-Di-O-tert-butyldimethylsilyl Paricalcitol 18-Aldehyde 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 FormulaC33H60O3Si2
Molecular Weight561.00 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990

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