2,4,6-Tri-tert-butylbenzene-1-sulfonyl chloride CAS 159539-19-2

Purity 97%+In StockPharmaceutical Standards
CAS No.159539-19-2
Molecular FormulaC18H29ClO2S
Molecular Weight344.94 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,4,6-Tri-tert-butylbenzene-1-sulfonyl chloride CAS 159539-19-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 344.94 g/mol gives 2,4,6-Tri-tert-butylbenzene-1-sulfonyl chloride distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

2,4,6-Tri-tert-butylbenzene-1-sulfonyl chloride (CAS 159539-19-2) is a high-purity analytical reference standard with the molecular formula C18H29ClO2S and a molecular weight of 344.94 g/mol.

Structurally, 2,4,6-Tri-tert-butylbenzene-1-sulfonyl chloride (C18H29ClO2S) contains a steroid core, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. 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 344.94 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

CATO manufactures 2,4,6-Tri-tert-butylbenzene-1-sulfonyl chloride under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC18H29ClO2S
Molecular Weight344.94 g/mol
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2002
Halogen ContentCl-containing
Sulfur Atoms1

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