ChemicalBook >> CAS DataBase List >>P-Toluenesulfonic anhydride

P-Toluenesulfonic anhydride

CAS No.
4124-41-8
Chemical Name:
P-Toluenesulfonic anhydride
Synonyms
4-Methylbenzenesulfonic anhydride;Tosic anhydride;p-Tolylsulfonyl 4-methylbenzenesulfonate;4-TOLUENESULFONIC ANHYDRIDE;Toluene-p-anhydride;3-Toluenesulfonicanhydride;p-Toluenesulfonyl anhydride;P-TOLUENESULFONIC ANHYDRIDE;TOLUENE-4-SULFONIC ANHYDRIDE;P-TOLUENESULPHONIC ANHYDRIDE
CBNumber:
CB1292293
Molecular Formula:
C14H14O5S2
Molecular Weight:
326.38
MDL Number:
MFCD00008548
MOL File:
4124-41-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 23:24:51

P-Toluenesulfonic anhydride Properties

Melting point 121-127 °C(lit.)
Boiling point 478.0±48.0 °C(Predicted)
Density 1.361±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
form Powder, Crystals and/or Chunks
color Off-white to gray
Sensitive Moisture Sensitive
BRN 2223702
InChI 1S/C14H14O5S2/c1-11-3-7-13(8-4-11)20(15,16)19-21(17,18)14-9-5-12(2)6-10-14/h3-10H,1-2H3
InChIKey PDVFSPNIEOYOQL-UHFFFAOYSA-N
SMILES Cc1ccc(cc1)S(=O)(=O)OS(=O)(=O)c2ccc(C)cc2
CAS DataBase Reference 4124-41-8(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C
Risk Statements  34
Safety Statements  26-36/37/39-45
RIDADR  UN 2585 8/PG 3
WGK Germany  3
10-21
Hazard Note  Irritant
HazardClass  8
PackingGroup  II
HS Code  29041000
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Eye Dam. 1
Skin Corr. 1B
NFPA 704
1
3 0

P-Toluenesulfonic anhydride price More Price(70)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 259764 p-Toluenesulfonic anhydride 97% 4124-41-8 5g $60.1 2026-04-30 Buy
Sigma-Aldrich 259764 p-Toluenesulfonic anhydride 97% 4124-41-8 25g $155 2026-04-30 Buy
TCI Chemical T1485 p-Toluenesulfonic Anhydride >95.0%(T) 4124-41-8 5g $28 2026-04-30 Buy
TCI Chemical T1485 p-Toluenesulfonic Anhydride >95.0%(T) 4124-41-8 25g $134 2026-04-30 Buy
Biosynth FT28875 p-Toluenesulfonic anhydride 4124-41-8 0.05kg $398.75 2026-06-04 Buy
Product number Packaging Price Buy
259764 5g $60.1 Buy
259764 25g $155 Buy
T1485 5g $28 Buy
T1485 25g $134 Buy
FT28875 0.05kg $398.75 Buy

P-Toluenesulfonic anhydride Chemical Properties, Uses, Production

Chemical Properties

Off-white to cream powder

Uses

p-Toluenesulfonic anhydride has been employed as reagent in palladium-catalyzed allylic alkenylation of allylic alcohols with n-butyl acrylate.

Reactions

Used as Reagent for tosylation.
p-Toluenesulfonic anhydride is a reliable way for the tosylation of many nucleophiles, primarily, for alcohols. The regent is a shelf-stable, well-soluble solid and “softer” electrophile than p-toluenesulfonyl chloride. Lipophilic alcohols can be easily tosylated in a very economical and eco-friendly way simply by using Ts2O in water without any catalyst. The tosylation can be realized in a few minutes under microwave assistance, giving p-toluenesulfonic acid as the only byproduct[1]. Besides, it can be applied as an additive in palladium-catalyzed allylic alkenylation of allylic alcohols.
Reaction of P-Toluenesulfonic anhydride

General Description

p-Toluenesulfonic anhydride acts as electrophilic species and activates 2-deoxy-sugar hemiacetals in situ, which reacts stereoselectively with nucleophilic acceptors to afford β-anomers.

Chemical Reactivity

4-Toluenesulfonic anhydride has a high chemical reactivity towards common nucleophilic reagents. It can undergo sulfonylation reaction with alcohol hydroxyl groups or amine compounds under alkaline conditions.

Synthesis

Add p-toluenesulfonic acid and an m-phosphorous compound used as raw materials into a reaction kettle, dropwise adding thionyl chloride while stirring. Controlling the temperature in the reaction kettle at 68-76 ℃ and heating to perform condensation after dropwise addition; inputting water and hydrochloric acid into the reaction kettle, cooling to 0 ℃. The reaction solution generated in the previous step was drawn into the water, vacuum filtration was performed, and centrifuging was used to obtain a crude product, p-toluenesulfonic anhydride. Furthermore, it was inputting ethyl acetate, performing heating reflux, and freezing to perform crystallization, thus obtaining the qualified finished product.

References

[1] OLIVERIO M, COSTANZO P, PAONESSA R, et al. Catalyst-free tosylation of lipophilic alcohols in water†[J]. RSC Advances, 2012, 8: 2548-2552. DOI:10.1039/C2RA23067D.

55865-38-8
104-15-4
359-65-9
4124-41-8
52723-97-4
Synthesis of P-Toluenesulfonic anhydride from Phosphinous amide, N,N-diethyl-P,P-bis(trifluoromethyl)- and p-Toluenesulfonic acid
Global Suppliers ( 357)
Supplier Tel Email Country ProdList Advantage
Shaoxing Fangxiao Chemical Co., LTD +86-13456999252; 13456999252 shellyhouse39@126.com China 41 58
Shanghai yongzeng technology co., LTD 021-021-021-65281118 15921781258 sales@yongzchem.com China 70 58
Shanghai Guoyuan Chemical Co., Ltd. 0512-55170668; 13913095008 shgyhg@139.com China 486 58
Hangzhou Copiore Chemical Co., Ltd. 17300981287 13757145729 sales@copiore.com China 291 58
ZOUPING MINGYUAN IMP.&EXP. TRADE CO.,LTD. 18364991597 fox793@163.com China 21 58
Shaanxi Weiyu New Materials Co., Ltd 13772052144 13772052144 308828748@qq.com China 3000 58
Taizhou Xinhongchuan New Material Co., Ltd 18651157028 18651157028 2579548755@qq.com China 1365 58
Creasyn Finechem(Tianjin) Co., Ltd. 022-83946278 13820372920 sales@creasyn.com China 968 68
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62

Related articles

View Latest Price from P-Toluenesulfonic anhydride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
P-Toluenesulfonic anhydride pictures 2026-09-09 P-Toluenesulfonic anhydride
4124-41-8
25kg 98% 500 Shanghai Yongzeng Technology Co.,Ltd
4-Methylbenzenesulfonic Anhydride pictures 2026-09-02 4-Methylbenzenesulfonic Anhydride
4124-41-8
$6.00 1KG 99% Henan Fengda Chemical Co., Ltd
P-Toluenesulfonic anhydride pictures 2026-08-07 P-Toluenesulfonic anhydride
4124-41-8
$1.00-50.00 1KG 99%+ 500KG Shaanxi Dideu Medichem Co. Ltd
P-TOLUENESULPHONIC ANHYDRIDE TOLUENE-4-SULFONIC ANHYDRIDE 1,3-BIS(4-METHYLPHENYL)-1,1,3,3-TETRAOXO-1LAMBDA6,3LAMBDA6-DITHIOXANE 4-TOLUENESULPHONIC ANHYDRIDE toluene-p-sulphonic anhydride 4-Toluenesulphonic acid anhydride 3-Toluenesulfonicanhydride Toluene-4-sulphonic anhydride 95% p-Toluenesulfonic anhydride 5GR (4-Methylphenyl)sulfonyl 4-methylbenzenesulfonate Toluene-4-sulfonic acid anhydride Toluene-p-anhydride Bis(4-methylbenzenesulfonic)anhydride Bis(p-toluenesulfonic)anhydride Di-p-toluenesulfonic anhydride p-Toluenesulfonic Anhydride p-Toluenesulfonyl anhydride (4-Methylbenzene)sulfonyl 4-Methylbenzene-1-sulfonate 4-Methylbenzenesulphonic anhydride, Tosic anhydride Toluene-4-sulphonic anhydride p-Toluenesulfonic anhydride 97% p-Methylbenzenesulfonic anhydride p-Toluenesulfonic anhydride, 98%+ p-Toluenesulfonic anhydride, 95%, for synthesis Benzenesulfonic acid, 4-methyl-, 1,1'-anhydride High Quality Pharmaceutical Intermediates P-Toluenesulfonic Anhydride 7-butoxybenzene-sulfonylchloride p-Toluenesulfonic anhydride (6CI, 7CI, 8CI) Toluenesulfonic anhydride (stored in the freezer, easy to decompose at high temperatures) P-TOLUENESULFONIC ANHYDRIDE 4-TOLUENESULFONIC ANHYDRIDE 4-Methylbenzenesulfonic anhydride p-Tolylsulfonyl 4-methylbenzenesulfonate Tosic anhydride 4124-41-8 CH3C6H4SO22O C14H14O5S2 Protection & Derivatization Reagents (for Synthesis) Building Blocks Organic Building Blocks Sulfur Compounds Sulfonic/Sulfinic Acid Anhydrides Pyridines Sulfonic/Sulfinic Acid Anhydrides Building Blocks Chemical Synthesis Organic Building Blocks Sulfur Compounds Protection & Derivatization Reagents (for Synthesis) Synthetic Organic Chemistry Organic Building Blocks Sulfonic/Sulfinic Acid Anhydrides Sulfur Compounds bc0001