2,4,6-Triisopropylbenzenesulfonyl chloride

2,4,6-Triisopropylbenzenesulfonyl chloride
  • CAS No.:6553-96-4

Important Notice

  1. This product is a chemical product/pharmaceutical intermediate. It is not a drug, an active pharmaceutical ingredient (API), or a pharmaceutical-grade material. It has not been granted a drug approval number or a Chemical Drug Substance Approval Notice, has not passed drug-related review and approval, and is not manufactured, tested, or released in accordance with pharmaceutical GMP.
  2. This product is intended solely for non-clinical research, process development, quality studies, further chemical processing, or chemical synthesis. It must not be used in drug-product manufacturing, clinical trials, clinical diagnosis, or administration to humans or animals, or be sold, used as an input, submitted for regulatory filing, or released as an API or pharmaceutical material.
  3. The purchaser must not use this product, or supply it to another party, for personal consumption, sports or fitness, weight loss, health supplements, food, or animal feed.
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2,4,6-Triisopropylbenzenesulfonyl chloride Basic information
Product Name:2,4,6-Triisopropylbenzenesulfonyl chloride
Synonyms:TPSCL 2,4,6-TRIISOPROPYLBENZENESULFONYL HYDRAZIDE;2,4,6-TRIISOPROPYLBENZENESULFONYL CHLORI;2,4,6-Tris(isopropyl)benzenesulphonyl chloride 98+%;2,4,6-Tris(prop-2-yl)benzenesulphonyl chloride;2,4,6-tris(propan-2-yl)benzene-1-sulfonyl chloride;2,4,6-three isopropylbenzene sulfonyl chloride;2,4,6-TRIISOPROPYLBENZENESULFONYL CHLORIDE97%;2,4,6-Triisopropylbenzenesulfonic acid chloride
CAS:6553-96-4
MF:C15H23ClO2S
MW:302.86
EINECS:229-479-6
Product Categories:API intermediates;Biochemistry;Condensation & Active Esterification;Condensing Agents (DNA / RNA Synthesis);Nucleosides, Nucleotides & Related Reagents;Protecting Agents, Phosphorylating Agents & Condensing Agents;Sulfur Compounds (for Synthesis);Synthetic Organic Chemistry;Organic Building Blocks;Sulfonyl Halides;Sulfur Compounds;Sulfonyl Halides;Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfur Compounds
Mol File:6553-96-4.mol
2,4,6-Triisopropylbenzenesulfonyl chloride Chemical Properties
Melting point 92-94 °C (lit.)
Boiling point 378C
density 1.1012 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility ethanol: 50 mg/mL, clear
form Crystalline Solid
color White to slightly beige
Water Solubility decomposes
Sensitive Moisture Sensitive
BRN 1218575
InChIKeyJAPYIBBSTJFDAK-UHFFFAOYSA-N
CAS DataBase Reference6553-96-4(CAS DataBase Reference)
Safety Information
Hazard Codes C
Risk Statements 34-29
Safety Statements 26-36/37/39-45-27
RIDADR UN 3261 8/PG 2
WGK Germany 3
F 21
Hazard Note Corrosive
HazardClass 8
PackingGroup II
HS Code 29049020
MSDS Information
ProviderLanguage
2,4,6-Triisopropylbenzenesulfonyl chloride English
SigmaAldrich English
ACROS English
ALFA English
2,4,6-Triisopropylbenzenesulfonyl chloride Usage And Synthesis
Chemical PropertiesWhite to cream solid
Uses2,4,6-Triisopropylbenzenesulfonyl chloride is used for the synthesis of glycerophospholipids as a condensing agent and in the analysis of phosphonolipids in egg yolk by HPLC/MS technique. It acts as a coupling reagent for the synthesis of oligonucleotides and as sulfonates of pyrimidine nucleosides. It also serves as a condensing agent in the synthesis of hydrogen-phosphonate diesters.
Uses2,4,6-Triisopropylbenzenesulfonyl chloride can be used in the analysis of phosphonolipids in eggyolk by HPLC/MS technique. It can also be used to synthesize:
  • Dimeric neomycin-neomycin conjugate with a flexible linker, 2,2′-(ethylenedioxy)bis(ethylamine).
  • Coupling reagents for the synthesis of oligonucleotides.
  • Sulfonates of pyrimidine nucleosides. These sulfonates can be displaced by nucleophiles in the presence of palladium-catalysts.
2,4,6-Triisopropylbenzenesulfonyl chloride Preparation Products And Raw materials
Raw materialsDiethyl ether-->Chloroform-->Magnesium sulfate-->Sodium chloride-->Benzene-->Aluminum chloride-->Chlorosulfonic acid-->Phosphorus pentoxide-->Pentane-->2-Bromopropane-->1,3,5-Triisopropylbenzene
Preparation Products2,4,6-Triisopropylbenzene-sulfonyl azide

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