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126-83-0

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  • China Biggest factory Supply High Quality 3-CHLORO-2-HYDROXYPROPANESULFONIC ACID SODIUM SALT CAS 126-83-0

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126-83-0 Usage

Chemical Properties

White crystalline powder

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 126-83-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126-83:
(5*1)+(4*2)+(3*6)+(2*8)+(1*3)=50
50 % 10 = 0
So 126-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H7ClO4S.Na/c4-1-3(5)2-9(6,7)8;/h3,5H,1-2H2,(H,6,7,8);/q;+1/p-1

126-83-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium 3-Chloro-2-hydroxypropanesulfonate

1.2 Other means of identification

Product number -
Other names 3-Chloro-2-hydroxypropanesulfonic acid,sodium salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:126-83-0 SDS

126-83-0Synthetic route

epichlorohydrin
106-89-8

epichlorohydrin

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

Conditions
ConditionsYield
With sodium hydrogensulfite In water at 85℃;80.6%
With sodium hydrogensulfite In water
With sodium hydrogen sulfate In water
sodium metabisulfite

sodium metabisulfite

epichlorohydrin
106-89-8

epichlorohydrin

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

Conditions
ConditionsYield
In sodium hydroxide; water50%
In sodium hydroxide; water50%
1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

Na2SO3

Na2SO3

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

Conditions
ConditionsYield
With water
epichlorohydrin
106-89-8

epichlorohydrin

NaHSO3

NaHSO3

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

Conditions
ConditionsYield
With water at 15℃;
beim Erhitzen auf dem Wasserbad;
sodium hydrogensulfite

sodium hydrogensulfite

epichlorohydrin
106-89-8

epichlorohydrin

sodium sulfite
7757-83-7

sodium sulfite

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

Conditions
ConditionsYield
In water424.0 g (82%)
sodium hydrogensulfite

sodium hydrogensulfite

epichlorohydrin
106-89-8

epichlorohydrin

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

Conditions
ConditionsYield
In not given 100°C;
In not given 100°C;
epoxychloropropane
66794-22-7

epoxychloropropane

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

Conditions
ConditionsYield
With sodium sulfate under 1034.32 Torr; Inert atmosphere; Heating;
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

dimethyl amine
124-40-3

dimethyl amine

3-(dimethylamino)-2-hydroxy-1-propanesulfonic acid sodium salt

3-(dimethylamino)-2-hydroxy-1-propanesulfonic acid sodium salt

Conditions
ConditionsYield
In water at 2.8 - 20℃;100%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-erucamidopropyl-N,N-dimethylamine
149968-48-9

N-erucamidopropyl-N,N-dimethylamine

erucyl dimethylamidopropyl hydroxy sulfobetaine
164118-71-2

erucyl dimethylamidopropyl hydroxy sulfobetaine

Conditions
ConditionsYield
With sodium hydroxide In water; isopropyl alcohol at 78℃; for 12h;92%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-methyldodecylamine
7311-30-0

N-methyldodecylamine

2-hydroxy-3-(N-methyldodecylammonio)propanesulfonate
1414933-00-8

2-hydroxy-3-(N-methyldodecylammonio)propanesulfonate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 130℃; for 24h; Inert atmosphere;91%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

Dimethyl-((E)-octadec-9-enyl)-amine

Dimethyl-((E)-octadec-9-enyl)-amine

C23H47NO4S

C23H47NO4S

Conditions
ConditionsYield
at 80℃; for 6h;90.43%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

tris(4-aza-2-hydroxydodecyl)amine
175897-85-5

tris(4-aza-2-hydroxydodecyl)amine

butan-1-ol
71-36-3

butan-1-ol

tris(4-aza-2,6-dihydroxy-4-octyl-7-sulfoheptyl)amine

tris(4-aza-2,6-dihydroxy-4-octyl-7-sulfoheptyl)amine

Conditions
ConditionsYield
In ethanol88.2%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

C31H56N2O

C31H56N2O

C34H62N2O5S

C34H62N2O5S

Conditions
ConditionsYield
In methanol at 130℃; under 2250.23 Torr; for 10h;88%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-(2-perfluorobutyl)ethyl dipropylamine

N-(2-perfluorobutyl)ethyl dipropylamine

C15H24F9NO4S

C15H24F9NO4S

Conditions
ConditionsYield
In isopropyl alcohol for 14h; Reflux;88%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-(1,1,2,3,3,4,4,5,5-decafluorobutyl)dipropylamine

N-(1,1,2,3,3,4,4,5,5-decafluorobutyl)dipropylamine

C16H23F12NO4S

C16H23F12NO4S

Conditions
ConditionsYield
In water; isopropyl alcohol for 16h; pH=9; Reflux;87.8%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-perfluorohexyldiethanolamine

N-perfluorohexyldiethanolamine

C11H12F13NO6S

C11H12F13NO6S

Conditions
ConditionsYield
In water; isopropyl alcohol for 16h; pH=9; Reflux;86.2%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-(2-perfluorohexyl)methyl diethanolamine

N-(2-perfluorohexyl)methyl diethanolamine

C14H18F13NO6S

C14H18F13NO6S

Conditions
ConditionsYield
In water; isopropyl alcohol for 16h; pH=9; Reflux;85.7%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

sodium 2,3-epoxypropanesulfonate

sodium 2,3-epoxypropanesulfonate

Conditions
ConditionsYield
With sodium phosphate In water at 55℃; for 4h;85.2%
With sodium phosphate In water at 55℃; for 4h;
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-(2-perfluorohexyl)ethyl diallylamine

N-(2-perfluorohexyl)ethyl diallylamine

C17H20F13NO4S

C17H20F13NO4S

Conditions
ConditionsYield
In water; isopropyl alcohol for 16h; pH=9; Reflux;85.2%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-1-octyl diethanolamine
27607-35-8

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluoro-1-octyl diethanolamine

C15H20F13NO6S

C15H20F13NO6S

Conditions
ConditionsYield
In water; isopropyl alcohol for 16h; pH=9; Reflux;84.4%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-ethyl-m-toulidine
102-27-2

N-ethyl-m-toulidine

N-ethyl-N-(2-hydroxy-3-sulfonatopropyl)-3-methylaniline sodium salt
82692-93-1

N-ethyl-N-(2-hydroxy-3-sulfonatopropyl)-3-methylaniline sodium salt

Conditions
ConditionsYield
With sodium hydroxide In water; isopropyl alcohol for 3h; Heating;83.4%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-(2-perfluorobutyl)ethyl dibenzylamine

N-(2-perfluorobutyl)ethyl dibenzylamine

C23H24F9NO4S

C23H24F9NO4S

Conditions
ConditionsYield
In water; isopropyl alcohol for 18h; pH=9; Reflux;83.2%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(2-di-methylaminoethyl)propanamide

3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(2-di-methylaminoethyl)propanamide

3-({2-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanamido]ethyl}-N,N-dimethylammonium)-2-hydroxypropane-1-sulfonate

3-({2-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanamido]ethyl}-N,N-dimethylammonium)-2-hydroxypropane-1-sulfonate

Conditions
ConditionsYield
Stage #1: sodium 3-chloro-2-hydroxypropane-sulfonate; 3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(2-di-methylaminoethyl)propanamide In water; isopropyl alcohol for 6h; Reflux;
Stage #2: With sodium carbonate In water; isopropyl alcohol for 7h; Reflux;
83%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N,N-dimethyl-2-propen-1-amine
2155-94-4

N,N-dimethyl-2-propen-1-amine

C8H17NO4S

C8H17NO4S

Conditions
ConditionsYield
In ethanol at 80℃; for 12h; Temperature; Inert atmosphere;83%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-di-methylaminopropyl)propanamide

3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-di-methylaminopropyl)propanamide

3-({3-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanamido]propyl}-N,N-dimethylammonium)-2-hydroxypropane-1-sulfonate

3-({3-[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propanamido]propyl}-N,N-dimethylammonium)-2-hydroxypropane-1-sulfonate

Conditions
ConditionsYield
Stage #1: sodium 3-chloro-2-hydroxypropane-sulfonate; 3-(3,5-di-tert-butyl-4-hydroxyphenyl)-N-(3-di-methylaminopropyl)propanamide In water; isopropyl alcohol Reflux;
Stage #2: With sodium carbonate In water; isopropyl alcohol Reflux;
80%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-ethyl-N-phenylamine
103-69-5

N-ethyl-N-phenylamine

sodium salt of N-ethyl-N-(2-hydroxy-3-sulfopropyl)aniline
82692-89-5

sodium salt of N-ethyl-N-(2-hydroxy-3-sulfopropyl)aniline

Conditions
ConditionsYield
With sodium hydroxide In water; isopropyl alcohol for 3h; Heating;79%
Quinuclidine
100-76-5

Quinuclidine

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

1-(3-sulfo-2-hydroxypropyl)quinuclidinium inner salt

1-(3-sulfo-2-hydroxypropyl)quinuclidinium inner salt

Conditions
ConditionsYield
Stage #1: Quinuclidine; sodium 3-chloro-2-hydroxypropane-sulfonate In 1,4-dioxane; water at 80℃; for 3h;
Stage #2: With Dowex 50x8
77%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

3,5-dimethyl-N-ethylaniline
13342-22-8

3,5-dimethyl-N-ethylaniline

sodium salt of 3,5-dimethyl-N-ethyl-N-(2-hydroxy-3-sulfopropyl)aniline
82692-97-5

sodium salt of 3,5-dimethyl-N-ethyl-N-(2-hydroxy-3-sulfopropyl)aniline

Conditions
ConditionsYield
With sodium hydroxide In water; isopropyl alcohol for 3h; Heating;68%
piperidine
110-89-4

piperidine

sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

2-hydroxy-3-piperidin-1-ylpropane-1-sulfonic acid

2-hydroxy-3-piperidin-1-ylpropane-1-sulfonic acid

Conditions
ConditionsYield
Stage #1: piperidine; sodium 3-chloro-2-hydroxypropane-sulfonate In water at 70 - 80℃; for 7h;
Stage #2: With Dowex 50x8
68%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

N-ethyl-m-anisidine
41115-30-4

N-ethyl-m-anisidine

sodium salt of N-ethyl-N-(2-hydroxy-3-sulfopropyl)-m-anisidine
82692-96-4

sodium salt of N-ethyl-N-(2-hydroxy-3-sulfopropyl)-m-anisidine

Conditions
ConditionsYield
With sodium hydroxide In water; isopropyl alcohol for 3h; Heating;65%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

oxiranyl-methanol
556-52-5

oxiranyl-methanol

1-hydroxy-2-sulfoethyl-N,N-dimethyl-N-(2,3-dihydroxypropyl)-N-methaneaminium hydroxide

1-hydroxy-2-sulfoethyl-N,N-dimethyl-N-(2,3-dihydroxypropyl)-N-methaneaminium hydroxide

Conditions
ConditionsYield
With dimethyl amine In nitrogen; water65%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

3,5-dimethoxy-phenylethylamine
73674-62-1

3,5-dimethoxy-phenylethylamine

sodium salt of 3,5-dimethoxy-N-ethyl-N-(2-hydroxy-3-sulfopropyl)aniline
83777-30-4

sodium salt of 3,5-dimethoxy-N-ethyl-N-(2-hydroxy-3-sulfopropyl)aniline

Conditions
ConditionsYield
With sodium hydroxide In water; isopropyl alcohol for 3h; Heating;61%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

tert-butylamine
75-64-9

tert-butylamine

3-(tert-butylamino)-2-hydroxy-1-propanesulfonic acid

3-(tert-butylamino)-2-hydroxy-1-propanesulfonic acid

Conditions
ConditionsYield
Stage #1: sodium 3-chloro-2-hydroxypropane-sulfonate; tert-butylamine In methanol; water at 35 - 45℃; for 3.56h;
Stage #2: With Dowex 50x8
59%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

benzylamine
100-46-9

benzylamine

1-(N-benzylamino)-2-hydroxy-1-propanesulfonic acid sodium salt

1-(N-benzylamino)-2-hydroxy-1-propanesulfonic acid sodium salt

Conditions
ConditionsYield
In 1,4-dioxane; water at 80℃; for 4.5h;50%
sodium 3-chloro-2-hydroxypropane-sulfonate
126-83-0

sodium 3-chloro-2-hydroxypropane-sulfonate

(3-tert-butyl-4-methoxybenzyl)-piperazine dihydrochloride

(3-tert-butyl-4-methoxybenzyl)-piperazine dihydrochloride

3-(1-(3-tert-butyl-4-methoxybenzyl)piperazine-4-yl)-2-hydroxy-1-propanesulfonic acid potassium salt
1383744-17-9

3-(1-(3-tert-butyl-4-methoxybenzyl)piperazine-4-yl)-2-hydroxy-1-propanesulfonic acid potassium salt

Conditions
ConditionsYield
Stage #1: (3-tert-butyl-4-methoxybenzyl)-piperazine dihydrochloride With potassium hydrogencarbonate In water
Stage #2: sodium 3-chloro-2-hydroxypropane-sulfonate With potassium iodide In water for 5h; Reflux;
45%

126-83-0Relevant articles and documents

Synthesis and properties of lauric acid-2-hydroxy-3-propane sulfonic acid sodium salt

Hao, Yulan,Yuan, Dandan,Wang, Yan,Qi, Ying,Zhang, Rongming

, p. 4449 - 4451 (2014)

The lauric acid-2-hydroxy-3-propane sulfonic acid sodium salt was synthesized by using sodium bisulfite, epichlorohydrin, sodium phosphate and lauric acid. The influence factors on reaction temperature, reaction time, the amount of catalyst and reactant molar ratio to the yield were investigated. The favorable conditions of synthesizing were determined:epichlorohydrin was added into the solution of sodium bisulfite of 85 °C, stirring for 2 h and left for 1.5 h. 3-Chloro-2-hydroxy-propane sulfonic acid sodium was synthesized. 3-Chloro-2-hydroxy-propane sulfonic acid sodium was mixed into the solution of sodium phosphate at 55 °C and 4 h reaction time. The 2,3-oxiranemethane sulfonic acid sodium salt was formed. 2,3-Oxiranemethane sulfonic acid sodium salt solution was dropped into the solution of lauric acid at 90 °C, the dropping time 0.5 h and left for 2.5 h. Lauric acid-2-hydroxy-3-propane sulfonic acid sodium salt was obtained. The yield was 85.2 % and was characterized by FTIR.

Synthesis, characterization and performance of unsaturated long-chain carboxybetaine and hydroxy sulfobetaine

Dong, Shuang-Jian,Li, Yun-Ling,Song, Yong-Bo,Zhi, Li-Fei

, p. 523 - 529 (2013)

The unsaturated long-chain carboxybetaine and hydroxy sulfobetaine were synthesized by the reaction of unsaturated octadecyl tertiary amine with sodium chloroacetate and 3-chloro-2-hydroxypropanesulfonic acid sodium salt, respectively. The structures of the two betaines were characterized by IR and 1H-NMR spectroscopy. The Krafft points of the two betaines are below 0 C and the isoelectric points are at pH 8.2 and 8.0, respectively. The surface tensions (γ CMC) at the critical micelle concentrations (CMC) were measured to investigate the surface activities of the prepared compounds when the pH is equal to 4.0, 6.5 and 10.0 at 50 C, respectively. Meanwhile, the corresponding saturated betaines were synthesized and determined for comparison. The double bond in the non-polar tail leads to a slightly higher CMC and a lower γ CMC. Though the CMC of the unsaturated betaine is slightly higher than that of saturated betaine for the double bond in the non-polar tail, the applied range of the unsaturated betaine is broader than corresponding saturated betaine for low Krafft point. The CMC and ΓCMC of the four betaines increase, but the pC20 decreases, with increasing pH. As a whole, the impact of pH on the performance of the four betaines is not very obvious.

Ammonium sulfonate zwitterionic silane coupling agent, siloxane ring body and preparation method of ammonium sulfonate zwitterionic silane coupling agent and siloxane ring body

-

Paragraph 0039-0040; 0051; 0052-0053; 0065-0066, (2020/02/29)

The invention discloses an ammonium sulfonate zwitterionic silane coupling agent and a preparation method thereof, and a siloxane ring body and a preparation method thereof, wherein the structure formulas of the ammonium sulfonate zwitterionic silane coupling agent and a first intermediate and a second intermediate for preparing the ammonium sulfonate zwitterionic silane coupling agent are respectively represented by a formula (1), a formula (2) and a formula (3), R is C1-C3 alkyl, a is 0, 1 or 2, and R and R are methyl or ethyl. According to the invention, the ammonium sulfonate zwitterionic silane coupling agent and the siloxane ring body meet the application requirements of chemical modification and graft modification on the surface of materials, and can be commercialized. Theinvention further provides a method capable of efficiently synthesizing the zwitterionic ammonium sulfonate type ionic silane coupling agent and the siloxane ring body.

Amide quaternary ammonium salt sodium hydroxypropyl sulfonate asphalt emulsifier and preparation method thereof

-

Paragraph 0053; 0056; 0066; 0075; 0083, (2018/05/01)

The invention discloses an amide quaternary ammonium salt sodium hydroxypropyl sulfonate asphalt emulsifier and a preparation method thereof. The asphalt emulsifier is prepared from coconut oil acyl propyl dimethyl tertiary amine, alcohol solvent, acrylic acid, epoxy chloropropane and sodium hydrogen sulfite according to a molar ratio of 1mol:(4.00-9.00)mol):(1.00-1.10)mol:(1.0-1.15)mol:(1.05-1.25)mol, wherein the alcohol solvent is alcohol, methanol or isopropanol. The asphalt emulsifier is easy-to-obtain in synthesis raw materials, low in production cost, simple in process and needless of high-temperature reaction and can emulsify asphalt different in type, emulsified asphalt prepared by using the asphalt emulsifier is exquisite, uniform and high in storage stability, and cationic emulsified asphalt can be prepared.

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