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N-(tert-Butoxycarbonyl)-p-toluenesulfonamide

CAS No.
18303-04-3
Chemical Name:
N-(tert-Butoxycarbonyl)-p-toluenesulfonamide
Synonyms
tert-Butyl tosylcarbamate;TsNBoc;tert-butyl N-(4-methylphenyl)sulfonylcarbamate;N-BOC-P-TOLUENESULFONAMIDE;LABOTEST-BB LT00453242;N-Boc-toluenesulfonamide;tert-Butyl N-tosylcarbamate;tert-Butyl N-(p-tosyl)carbamate;(tert-Butoxycarbonyl)tosylamine;N-Boc-4-methylbenzenesulfonamide
CBNumber:
CB1380558
Molecular Formula:
C12H17NO4S
Molecular Weight:
271.33
MDL Number:
MFCD00134267
MOL File:
18303-04-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:49:13

N-(tert-Butoxycarbonyl)-p-toluenesulfonamide Properties

Melting point 121-123 °C(lit.)
Density 1.201±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility chloroform: soluble25mg/mL, clear, colorless
pka 4.84±0.10(Predicted)
form powder to crystal
color White to Almost white
InChI InChI=1S/C12H17NO4S/c1-9-5-7-10(8-6-9)18(15,16)13-11(14)17-12(2,3)4/h5-8H,1-4H3,(H,13,14)
InChIKey DUTLOVSBVBGNDM-UHFFFAOYSA-N
SMILES C(OC(C)(C)C)(=O)NS(C1=CC=C(C)C=C1)(=O)=O
CAS DataBase Reference 18303-04-3
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Safety Statements  24/25
WGK Germany  3
HS Code  29350090
Storage Class 10 - Combustible liquids

N-(tert-Butoxycarbonyl)-p-toluenesulfonamide price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 363839 N-(tert-Butoxycarbonyl)-p-toluenesulfonamide 18303-04-3 25g $128 2026-04-30 Buy
Sigma-Aldrich 363839 N-(tert-Butoxycarbonyl)-p-toluenesulfonamide 18303-04-3 5g $55 2023-06-20 Buy
TCI Chemical B1648 N-(tert-Butoxycarbonyl)-p-toluenesulfonamide >98.0%(T) 18303-04-3 10g $92 2026-04-30 Buy
TCI Chemical B1648 N-(tert-Butoxycarbonyl)-p-toluenesulfonamide >98.0%(T) 18303-04-3 25g $172 2026-04-30 Buy
Chem-Impex 37119 N-(tert-Butoxycarbonyl)-p-toluenesulfonamide ≥98%(HPLC) 18303-04-3 1G $18.5 2026-05-19 Buy
Product number Packaging Price Buy
363839 25g $128 Buy
363839 5g $55 Buy
B1648 10g $92 Buy
B1648 25g $172 Buy
37119 1G $18.5 Buy

N-(tert-Butoxycarbonyl)-p-toluenesulfonamide Chemical Properties, Uses, Production

Description

N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE is an useful component in Mitsunobu reactions for the direct preparation of protected amines from alcohols.

Uses

N-(tert-Butoxycarbonyl)-p-toluenesulfonamide may be used in the preparation of enyne amide, precursor for Pauson-Khand reaction.

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 379, 1994 DOI: 10.1016/0040-4039(94)85058-5

General Description

N-(tert-Butoxycarbonyl)-p-toluenesulfonamide is a N-substituted sulphonamide and its reaction with N-trityl L-serine esters under Mitsunobu reaction conditions is reported. It can be directly coupled with primary, secondary and allylic alcohols under Mitsunobu conditions to afford various sulfonyl-protected amines.

storage

N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE can be stored for extended periods of time in an amber  bottle at rt.

N-(tert-Butoxycarbonyl)-p-toluenesulfonamide Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 128)
Supplier Tel Email Country ProdList Advantage
Shanghai Raise Chemical Technology Co.,Ltd 15026594951 rs@raise-chem.com China 4905 55
Aikon International Limited 17714375163 hywu@aikonchem.com China 9974 58
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
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Shanghai Longsheng chemical Co.,Ltd. 58099637 13585536065 sales@shlschem.com China 9880 59
jiliang chemicals 21-62165282 bidingchem@163.com China 1395 60
Maya High Purity Chemicals +86 (573) 82222445 (0)18006601000 452520369 sales@maya-r.com China 11693 57
TOKYO CHEMICAL INDUSTRY CO., LTD. 03-36680489 Sales-JP@TCIchemicals.com Japan 28364 80

View Latest Price from N-(tert-Butoxycarbonyl)-p-toluenesulfonamide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE  pictures 2026-08-20 N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE
18303-04-3
$1.10 1g 99.00% 100 Tons Min Dideu Industries Group Limited
N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE pictures 2025-04-04 N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE
18303-04-3
1KG 98% 1ton Henan Aochuang Chemical Co.,Ltd.
N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE pictures 2019-08-30 N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE
18303-04-3
$1.00 1KG 98% 200kg Career Henan Chemical Co
LABOTEST-BB LT00453242 N-(tert-Butoxycarbonyl-p-tolunesulfonamide (tert-Butoxycarbonyl)tosylamine N-(p-Tolylsulfonyl)carbamic acid tert-butyl ester N-Tosylcarbamic acid tert-butyl ester Tosylcarbamic acid tert-butyl ester N-Boc-toluenesulfonamide tert-Butyl N-(p-tosyl)carbamate tert-Butyl N-tosylcarbamate N-(tert-Butoxycarbonyl)-p-toluenesulfonamide N-Boc-4-methylbenzenesulfonamide Carbamic acid,N-[(4-methylphenyl)sulfonyl]-, 1,1-dimethylethyl ester N-Boc-p-toluenesulfonamide, 99%, for synthesis N-(tert-Butoxycarbonyl)-p-toluenesulfonamide > ert-butylN-(4-methylphenyl)sulfonylcarbamate N-(TERT-BUTOXYCARBONYL)-P-TOLUENESULFONAMIDE ISO 9001:2015 REACH N-(Tert-butoxycarbonyl)-P-toluenesulfonamide, 98+% N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide tert-butyl N-(p-tolylsulfonyl)carbamate tert-Butyl [(4-methylphenyl)sulfonyl]carbamate N-(tert-Butyloxycarbonyl)-p-toluenesulfonamide N-BOC-P-TOLUENESULFONAMIDE tert-butyl N-(4-methylphenyl)sulfonylcarbamate tert-Butyl tosylcarbamate TsNBoc N-(tert-Butoxycarbonyl)-p-toluenesulfonamide 18303-04-3 CH3C6H4SO2NHCO2CCH33 Nitrogen Compounds Organic Building Blocks Protected Amines Amination Building Blocks Amination Synthetic Organic Chemistry Nitrogen Compounds Organic Building Blocks Protected Amines