4,6-Di-tert-butylbenzene-1,3-diamine CAS 13733-14-7

Purity 97%+In StockPharmaceutical Standards
CAS No.13733-14-7
Molecular FormulaC14H24N2
Molecular Weight220.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4,6-Di-tert-butylbenzene-1,3-diamine CAS 13733-14-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 4,6-Di-tert-butylbenzene-1,3-diamine.

CATO supplies 4,6-Di-tert-butylbenzene-1,3-diamine (CAS 13733-14-7), a certified reference material (molecular formula C14H24N2, MW 220.35 g/mol) for analytical method development and quality control.

Structurally, 4,6-Di-tert-butylbenzene-1,3-diamine (C14H24N2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 220.35 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 4,6-Di-tert-butylbenzene-1,3-diamine 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 FormulaC14H24N2
Molecular Weight220.35 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1960
Nitrogen Atoms2

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