1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, ammonium salt

Base Information

Chemical Name:1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, ammonium salt
CAS No.:6381-61-9
Deprecated CAS:128-43-8
Molecular Formula:C7H5 N O3 S . H3 N
Molecular Weight:200.218
Hs Code.:
European Community (EC) Number:228-971-8
UNII:63Q3BCF15A
DSSTox Substance ID:DTXSID7027621
Mol file:6381-61-9.mol

Synonyms:Daramin;Saccharin ammonium;Saccharinate ammonium;6381-61-9;1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, ammonium salt;1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, ammonium salt (1:1);63Q3BCF15A;SUCLINE;AMMONIUM SACCHARIN [FCC];DTXSID7027621;ammonium 3-oxo-3H-1,2-benzisothiazol-2-ide 1,1-dioxide;SACCHARIN AMMONIUM SALT [MI];1,2-BENZISOTHIAZOLIN-3-ONE 1,1-DIOXIDE AMMONIUM SALT

Suppliers and Price of 1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, ammonium salt

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
1,2-BENZISOTHIAZOL-3-(2H)-ONE-1,1-DIOXIDE AMMONIUM SALT 95.00%
5MG
$ 501.34

Total 6 raw suppliers

Chemical Property of 1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, ammonium salt

Chemical Property:

Vapor Pressure:1.23E-07mmHg at 25°C
Refractive Index:1.6000 (estimate)
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：78.35000
Density:1.557g/cm³
LogP:1.53380
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:200.02556330
Heavy Atom Count:13
Complexity:314

Purity/Quality:

99% ^*data from raw suppliers

1,2-BENZISOTHIAZOL-3-(2H)-ONE-1,1-DIOXIDE AMMONIUM SALT 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): A severe eye irritant.
Hazard Codes:A severe eye irritant.

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=NS2(=O)=O)[O-].[NH4+]
Uses Food additive.

Technology Process of 1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, ammonium salt

There total 1 articles about 1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, ammonium salt which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 75.0%

: 26638-43-7
2-methoxycarbonylbenzenesulfonyl chloride

: 6381-61-9
ammonium saccharinate

Guidance literature:: With ammonium hydroxide; In methanol; at 40 ℃; for 3h;
DOI:10.1016/0022-328X(84)80135-7

Reference yield: 85.0%

: 6381-61-9
ammonium saccharin

: 639-58-7
triphenyltin chloride

: 83171-58-8
N-triphenylstannyl-4,5-benzisothiazol-3(2H)-one 1,1-dioxide

Guidance literature:: In methanol; byproducts: ammonium chloride; ammonium saccharin was added to a soln. of Ph3SnCl in anhyd. methanol, mixt. was refluxed for 1 h; filtered, filtrate evapd. in vacuo, NH4Cl was removed by washing several times with distilled water, recrystd. twice from methanol; elem. anal.;
DOI:10.1016/0022-328X(84)80135-7

Reference yield: 73.0%

: 6381-61-9
ammonium saccharin

: 1135-99-5
diphenyltin(IV) dichloride

: 91408-37-6
(C₆H₅)2Sn(NCOSO₂C₆H₄)2

Guidance literature:: In methanol; byproducts: ammonium chloride; ammonium saccharin was added to a soln. of Ph2SnCl2 in anhyd. methanol,mixt. was refluxed for 1 h; filtered, filtrate evapd. in vacuo, NH4Cl was removed by washing several times with distilled water, recrystd. twice from methanol; elem. anal.;
DOI:10.1016/0022-328X(84)80135-7