2-(2-((1H-Indol-3-yl)methyl)-4-(tert-butoxycarbonyl)piperazin-1-yl)acetic acid CAS 1060813-85-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1060813-85-5
Molecular FormulaC20H27N3O4
Molecular Weight373.45 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(2-((1H-Indol-3-yl)methyl)-4-(tert-butoxycarbonyl)piperazin-1-yl)acetic acid CAS 1060813-85-5 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.

CATO supplies 2-(2-((1H-Indol-3-yl)methyl)-4-(tert-butoxycarbonyl)piperazin-1-yl)acetic acid (CAS 1060813-85-5), a certified reference material (molecular formula C20H27N3O4, MW 373.45 g/mol) for analytical method development and quality control.

Structurally, 2-(2-((1H-Indol-3-yl)methyl)-4-(tert-butoxycarbonyl)piperazin-1-yl)acetic acid (C20H27N3O4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 373.45 g/mol, it falls into the moderately-high-molecular-weight range. 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), 2-(2-((1H-Indol-3-yl)methyl)-4-(tert-butoxycarbonyl)piperazin-1-yl)acetic acid 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 FormulaC20H27N3O4
Molecular Weight373.45 g/mol
AppearancePale yellow to 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms3

Related H Standards

Recommended Standards

Why CATO?