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p-Toluenesulfonyl Isocyanate

CAS No.
4083-64-1
Chemical Name:
p-Toluenesulfonyl Isocyanate
Synonyms
PTSI;TOSYL ISOCYANATE;p-Tosyl isocyanate;P-TOLUENESULPHONYL ISOCYANATE;4-TOLUENESULFONYL ISOCYANATE;Ptsl;MSI/PTSI;POLYLINK PTSI;PARA-TOSYLISOCYANATE;TOSYL ISOCYANATE (PTSI)
CBNumber:
CB8256995
Molecular Formula:
C8H7NO3S
Molecular Weight:
197.21
MDL Number:
MFCD00002030
MOL File:
4083-64-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 05:21:43
Product description Number Pack Size Price
p-Toluenesulfonyl isocyanate 97% 189278 25g $47.3
p-Toluenesulfonyl isocyanate 97% 189278 100g $49.7
p-Toluenesulfonyl Isocyanate >97.0%(T) T0998 25g $19
p-Toluenesulfonyl Isocyanate >97.0%(T) T0998 100g $32
p-Toluenesulfonyl isocyanate 289706 250g $408
More product size

p-Toluenesulfonyl Isocyanate Properties

Melting point 5°C
Boiling point 144 °C10 mm Hg(lit.)
Density 1.291 g/mL at 25 °C(lit.)
vapor pressure 1 mm Hg ( 100 °C)
refractive index n20/D 1.534(lit.)
Flash point >230 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form Liquid
color Clear colorless to yellow
Specific Gravity 1.291.291
Odor acrid odor
Water Solubility reacts
Sensitive Moisture Sensitive
BRN 391287
Henry's Law Constant 1.7×10-1 mol/(m3Pa) at 25℃, Zhang et al. (2010)
InChI 1S/C8H7NO3S/c1-7-2-4-8(5-3-7)13(11,12)9-6-10/h2-5H,1H3
InChIKey VLJQDHDVZJXNQL-UHFFFAOYSA-N
SMILES Cc1ccc(cc1)S(=O)(=O)N=C=O
LogP 0.6 at 30℃
CAS DataBase Reference 4083-64-1(CAS DataBase Reference)
FDA UNII H9004FJX6V
NIST Chemistry Reference 4-Methylbenzenesulfonyl isocyanate(4083-64-1)
EPA Substance Registry System Benzenesulfonyl isocyanate, 4-methyl- (4083-64-1)
UNSPSC Code 41116105
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
Signal word  Danger
Hazard statements  H315-H319-H334-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
Hazard Codes  Xn
Risk Statements  14-36/37/38-42
Safety Statements  26-28-30-28A
RIDADR  UN 2206 6.1/PG 3
WGK Germany  1
RTECS  DB9032000
10
TSCA  TSCA listed
HazardClass  6.1
PackingGroup  III
HS Code  29309090
Storage Class 10 - Combustible liquids
Hazard Classifications Eye Irrit. 2
Resp. Sens. 1
Skin Irrit. 2
STOT SE 3
REACH Registrations Active
NFPA 704
1
2 2
W

p-Toluenesulfonyl Isocyanate price More Price(50)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 189278 p-Toluenesulfonyl isocyanate 97% 4083-64-1 25g $47.3 2026-04-30 Buy
Sigma-Aldrich 189278 p-Toluenesulfonyl isocyanate 97% 4083-64-1 100g $49.7 2026-04-30 Buy
TCI Chemical T0998 p-Toluenesulfonyl Isocyanate >97.0%(T) 4083-64-1 25g $19 2026-04-30 Buy
TCI Chemical T0998 p-Toluenesulfonyl Isocyanate >97.0%(T) 4083-64-1 100g $32 2026-04-30 Buy
Usbiological 289706 p-Toluenesulfonyl isocyanate 4083-64-1 250g $408 2026-06-03 Buy
Product number Packaging Price Buy
189278 25g $47.3 Buy
189278 100g $49.7 Buy
T0998 25g $19 Buy
T0998 100g $32 Buy
289706 250g $408 Buy

p-Toluenesulfonyl Isocyanate Chemical Properties,Uses,Production

Chemical Properties

clear liquid

Uses

p-Toluenesulfonyl isocyanate is a reagent used to prepare acetylated syn-1,2-diols,1 oxazolidin-2-ones,2 2,3-diamino acids,3 and N-tosylcarbonamides.4

Uses

It is a reagent used to prepare acetylated syn-1,2-diols,oxazolidin-2-ones, 2,3-diamino acids, and N-tosylcarbonamides. -Toluenesulfonyl isocyanate has been used as derivatization reagent in determination of 3-α-hydroxy tibolone in human plasma by LC-MS/MS. It is also employed in the derivatization reagent in simultaneous quantitative analysis of diethylene glycol and propylene glycol in pharmaceutical products by HPLC and as reagent in the preparation of acetylated syn-1,2-diols, oxazolidin-2-ones, 2,3-diamino acids and N-tosylcarbonamides.

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 9609, 1994 DOI: 10.1016/0040-4039(94)88523-0

General Description

p-Toluenesulfonyl isocyanate undergoes palladium-catalyzed bis-allylation reaction with allylstannanes and allyl chlorides.

Reactivity Profile

p‐Toluenesulfonyl Isocyanate (PTSI) is recommended especially for one‐component, low‐VOC polyurethane coatings. The reaction of PTSI with water introduced from pigments and solvents in the paint formulation generates carbon dioxide and soluble inert chemical products. Experience has demonstrated that 13 grams of PTSI effectively scavenges 1 gram of water. PTSI reacts with water in a 1 to 1 molar ratio, generating PTSA and carbon dioxide gas. This reaction occurs readily at room temperature and does not require heating. The PTSA generated in the process is essentially an inert material that does not further react with PTSI or other isocyanate groups, resulting in the formation of insoluble ureas. The hydroxyl group is reacted with excess p-toluenesulfonyl isocyanate (TSI) to form an acidic carbamate. Water is added to convert unreacted isocyanate to sulfonamide, followed by direct potentiometric titration of the acidic carbamate with tetrabutylammonium hydroxide (Bu4NOH) in nonaqueous medium.
p-Toluenesulfonyl Isocyanate

Hazard

Moderately toxic by ingestion. Low toxicity by inhalation. A mild skin and moderate eye irritant.

Safety

Danger! Harmful if swallowed, inhaled or absorbed through the skin. Causes skin and severe eye irritation. It may cause an allergic respiratory response. Reacts spontaneously and violently with water, alcohols, amines, acids and alkaline solutions. These substances should not be poured into a vessel containing PTSI. Prolonged exposure of PTSI to elevated temperatures can result in violent decomposition. Temperatures above 170C are to be avoided. Reaction with water results in the generation of carbon dioxide. Reaction vessels should be vented to avoid pressure build‐up. Vent through a calcium chloride tube to prevent moisture from entering vessels. Do not get in the eyes, on the skin, or clothing. Avoid breathing vapour or mist. Keep the container closed. Use with adequate ventilation. Wash thoroughly after handling. If handled indoors, provide adequate mechanical exhaust ventilation or wear NIOSH/MSHA approved air ‐line respirator or SCBA. Wear impervious PVC or rubber gloves, goggles, and protective clothing. PTSI must be stored in air‐tight containers.

Synthesis

Add the organic azide 4-methylbenzenesulfonyl azide (0.75 mmol), Pd(OAc)2 (5.6 mg, 5 mol%) to an oven-dried Schlenk tube (10 mL). Purge the tube and backfill with CO (three cycles) from a balloon. Inject anhydrous MeCN (3.0 mL) into the tube. Stir at 80 ℃ for 4 h under the CO atmosphere (balloon). Concentrate the mixture under reduced pressure. Purify the residue by column chromatography (petroleum ether/EtOAc 3:1.-.1:1) to afford p-Toluenesulfonyl Isocyanate.Synthesis_4083-64-1

32315-10-9
70-55-3
4083-64-1
Synthesis of p-Toluenesulfonyl Isocyanate from Triphosgene and p-Toluenesulfonamide

p-Toluenesulfonyl Isocyanate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 485)Suppliers
Supplier Tel Email Country ProdList Advantage
SIMAGCHEM CORP
+86-5922680277 +86-13806087780 sale@simagchem.com China 17339 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +86-18949832763 info@tnjchem.com China 2984 55
Tianjin Zhongxin Chemtech Co., Ltd.
86-22-66880623 +8618622897568 sales@tjzxchem.com China 571 58
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 sales@amoychem.com China 6361 58
BLiT (Hefei)Chemical Co.,Ltd
+86-551-62622640 +86-19521662663 sales@blitchem.com China 292 58
Jinan Finer Chemical Co., Ltd
+86-531-88989536 +86-15508631887 sales@finerchem.com China 2949 58
Chemport Science Technology Shanghai) Co., Ltd.
+86-13816004845 chen@chemport-sh.com China 189 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 17389186172 1077@dideu.com China 3999 58
Hebei Chuanghai Biotechnology Co,.LTD
+86-86-13131129325 sales1@chuanghaibio.com China 5218 58
Hebei Chuanghai Biotechnology Co., Ltd
+86-17732866630 mina@chuanghaibio.com China 18114 58

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$75.00-100.00 1kg 99% 5000 HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
4-Isocyanatosulphonyltoluene, p-Toluenesulfonyl isocyanate, 96%, AcroSeal Isocyanicacid, anhydride with p-toluenesulfonic acid (6CI) p-Toluenesulfonyl isocyanate 96% p-Toluenesulfonyl isocyanate, 96%, SpcSeal p-Toluenesulfonylisocyanate,95% Benzenesulfonyl isocyanate, 4-methyl- Benzenesulfonylisocyanate,4-methyl- p-Methylphenylsulfonyl isocyanate p-Toluenesulfonic acid, anhydride with isocyanic acid p-Toluensulfonyl isocyanate p-Tolylsulfonyl isocyanate Sulfone, isocyanato tolyl P-TOLUENESULFONYL ISOCYANATE P-TOLUENESULPHONYL ISOCYANATE TOLUENE-4-SULFONYL ISOCYANATE 4-METHYLBENZENE-1-SULFONYL ISOCYANATE 4-methyl-benzenesulfonylisocyanat 4-methyl-Benzenesulfonylisocyanate 4-Methylphenylsulfonyl isocyanate PARA-TOSYLISOCYANATE p-Toluolsulfonylisocyanat P-toluenesulfonyl isocyanate (Tosyl isocyanate ,PTSI) p-Toluenesulfonyl Isocyanate, PTSI, Tosyl Isocyanate 4-isocyanatosulphonyltoluene tosyl isocyanate p-Toluenesulfonyl isocyanate,96% p-Toluenesulfonyl isocyanate, AcroSeal, 96% P-toluenesulfony6l isocyanate 4-methylbenzene-1-sulphonyl isocyanate Para Toluene Sulfonyl Isocyanate POLYLINK PTSI P-TOULENESULFONYL ISOCYANATE(TOULENESULFONYL ISOCYANATE) P-TOLUENESULFONYL ISOCYANATE(PTSI)98% TOSYL ISOCYANATE (PTSI) 4-METHYLBENZENESULPHONYLISOCYANATE P**P-TOLUENESULFONYL ISOCYANATE Ptsl 4-Methyl-N-(oxomethylene)benzenesulfonamide MSI/PTSI p-Toluenesulfonyl isocyanate, 96%, AcroSeal&trade 4-methyl-N-(oxomethylidene)benzenesulfonamide p-Toluenesulfonyl isocyanate Isocyanate p-toluenesulfonic acid p-Toluenesulfonyl isocyate 4-TOLUENESULFONYL ISOCYANATE p-Tosyl isocyanate PTSI TOSYL ISOCYANATE 4083-64-1 CH3C6H4SO2NCO ISOCYANATE Organic Building Blocks Sulfur Compounds (for Synthesis) Nitrogen Compounds Isocyanates Building Blocks Building Blocks Chemical Synthesis