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5138-18-1

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5138-18-1 Usage

Chemical Properties

viscous colourless liquid (generally supplied

Uses

Sulfosuccinic Acid is cosmetic compound.

Check Digit Verification of cas no

The CAS Registry Mumber 5138-18-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,3 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5138-18:
(6*5)+(5*1)+(4*3)+(3*8)+(2*1)+(1*8)=81
81 % 10 = 1
So 5138-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O7S/c5-3(6)1-2(4(7)8)12(9,10)11/h2H,1H2,(H,5,6)(H,7,8)(H,9,10,11)

5138-18-1 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (338567)  Sulfosuccinicacidsolution  70 wt. % in H2O

  • 5138-18-1

  • 338567-250ML

  • 720.72CNY

  • Detail
  • Aldrich

  • (338567)  Sulfosuccinicacidsolution  70 wt. % in H2O

  • 5138-18-1

  • 338567-1L

  • 2,177.37CNY

  • Detail

5138-18-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-sulfobutanedioic acid

1.2 Other means of identification

Product number -
Other names Acide sulfosuccinique

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:5138-18-1 SDS

5138-18-1Synthetic route

sodium sulfosuccinate

sodium sulfosuccinate

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With acid In water pH=< 1; Concentration;86%
potassium bisulfite

potassium bisulfite

bromosuccinic acid
923-06-8, 584-98-5

bromosuccinic acid

A

malic acid
617-48-1

malic acid

B

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

C

(2E)-but-2-enedioic acid
110-17-8

(2E)-but-2-enedioic acid

Conditions
ConditionsYield
heating, 18 h;A n/a
B 40%
C n/a
heating, 18 h;A n/a
B 40%
C n/a
bromosuccinic acid
923-06-8, 584-98-5

bromosuccinic acid

A

malic acid
617-48-1

malic acid

B

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With potassium disulphite; water at 100℃;
With potassium disulphite; water at 100℃; inactive sulfosuccinic acid;
succinic acid
110-15-6

succinic acid

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With sulfur trioxide
With sulfur trioxide at 40 - 50℃;
succinic acid
110-15-6

succinic acid

A

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

B

2,3-disulfosuccinic acid
54060-35-4

2,3-disulfosuccinic acid

Conditions
ConditionsYield
With sulfur trioxide at 40 - 50℃; inactive sulfosuccinic acid;
succinoyl dichloride
543-20-4

succinoyl dichloride

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With silver sulfate at 120 - 130℃; Behandlung des Reaktionsproduktes mit Wasser;
maleic acid
110-16-7

maleic acid

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With potassium sulfite
With potassium sulfite; water Dikaliumsalz der Sulfobernsteinsaeure entsteht;
(2E)-but-2-enedioic acid
110-17-8

(2E)-but-2-enedioic acid

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With potassium sulfite
disodium lauryl sulfosuccinate

disodium lauryl sulfosuccinate

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With hydrogen cation In water at 90℃; for 0.5h; Kinetics; degree of hydrolysis 26.5percent; further temperatures;
disodium Laureth Sulfosuccinate

disodium Laureth Sulfosuccinate

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With hydrogen cation In water at 90℃; for 0.5h; Kinetics; degree of hydrolysis 66.9percent; further temperatures;
hydrogenchloride
7647-01-0

hydrogenchloride

(2-amino-4-oxo-4,5-dihydro-thiazol-5-yl)-acetic acid
33176-41-9

(2-amino-4-oxo-4,5-dihydro-thiazol-5-yl)-acetic acid

barium chlorate

barium chlorate

A

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

B

urea
57-13-6

urea

water
7732-18-5

water

(2E)-but-2-enedioic acid
110-17-8

(2E)-but-2-enedioic acid

KHSO3

KHSO3

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
Reaktion von Kaliumfumarat;
DL-thiomalic acid
70-49-5

DL-thiomalic acid

nitric acid
7697-37-2

nitric acid

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

dipotassium fumarate

dipotassium fumarate

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With potassium bisulfite; water inactive sulfosuccinic acid;
dipotassium maleate

dipotassium maleate

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With potassium disulphite; water inactive sulfosuccinic acid;
pseudothiohydantoinacetic acid

pseudothiohydantoinacetic acid

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With hydrogenchloride; barium chlorate
thiomalic acid

thiomalic acid

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
With nitric acid
bromosuccinic acid
923-06-8, 584-98-5

bromosuccinic acid

water
7732-18-5

water

potassium meta bisulfite

potassium meta bisulfite

A

malic acid
617-48-1

malic acid

B

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
at 100℃;
succinic acid
110-15-6

succinic acid

sulfur trioxide (2.5-4 mol)

sulfur trioxide (2.5-4 mol)

A

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

B

disulfosuccinic acid

disulfosuccinic acid

Conditions
ConditionsYield
at 40 - 50℃;
succinic acid
110-15-6

succinic acid

sulfur trioxide (4.5 mol)

sulfur trioxide (4.5 mol)

A

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

B

maleic acid
110-16-7

maleic acid

C

disulfosuccinic acid

disulfosuccinic acid

Conditions
ConditionsYield
at 115℃;
potassium maleate dibasic
4151-34-2

potassium maleate dibasic

water
7732-18-5

water

potassium meta bisulfite

potassium meta bisulfite

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

bromosuccinic acid
923-06-8, 584-98-5

bromosuccinic acid

sodium sulfite
7757-83-7

sodium sulfite

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

Conditions
ConditionsYield
In not given alkaline Na2SO3 soln.;
In not given alkaline Na2SO3 soln.;
[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

copper(II) acetate monohydrate
6046-93-1

copper(II) acetate monohydrate

sodium hydroxide
1310-73-2

sodium hydroxide

poly[μ2-aqua-diaqua(2,2'-bipyridyl)(μ5-2-sulfonatobutanedioato)copper(II)sodium(I)]

poly[μ2-aqua-diaqua(2,2'-bipyridyl)(μ5-2-sulfonatobutanedioato)copper(II)sodium(I)]

Conditions
ConditionsYield
In ethanol; water EtOH soln. of 2,2'-bipyridyl carefully layered on top of aq. Cu acetate with naOH and acid; left for 1 wk; washed with EtOH, dried at ambient temp.;43%
sulfosuccinic acid
5138-18-1

sulfosuccinic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With potassium hydroxide
sulfosuccinic acid
5138-18-1

sulfosuccinic acid

(2E)-but-2-enedioic acid
110-17-8

(2E)-but-2-enedioic acid

Conditions
ConditionsYield
With potassium hydroxide
sulfosuccinic acid
5138-18-1

sulfosuccinic acid

sulfur trioxide
7446-11-9

sulfur trioxide

2,3-disulfosuccinic acid
54060-35-4

2,3-disulfosuccinic acid

Conditions
ConditionsYield
at 50℃; inactive sulfosuccinic acid;
sulfosuccinic acid
5138-18-1

sulfosuccinic acid

concentrated KOH-solution

concentrated KOH-solution

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

oxalic acid
144-62-7

oxalic acid

C

acetic acid
64-19-7

acetic acid

D

SO2

SO2

sulfosuccinic acid
5138-18-1

sulfosuccinic acid

potash

potash

A

(2E)-but-2-enedioic acid
110-17-8

(2E)-but-2-enedioic acid

B

SO2

SO2

5138-18-1Relevant articles and documents

Preparation method for sulfosuccinic acid

-

Paragraph 0006; 0009; 0010; 0012; 0013; 0015; 0016, (2018/06/21)

The invention discloses a preparation method for sulfosuccinic acid, which is characterized in that maleic anhydride is preheated under 70 DEG C to 90 DEG C, and 1.1 to 1.7 equivalent weight of sodiumhydrogen sulfite solution is slowly added into the preheated system; after addition, agitation is continued under 70 DEG C to 90 DEG C for 2 to 10 hours; the obtained reaction solution is sodium sulfosuccinate solution; the solution is added with water, so that 5 to 30 percent of sodium sulfosuccinate solution is prepared, and the sulfosuccinic acid is prepared by strongly acidic ion exchange resin. The advantages of the preparation method are as follows: by the method, a sulfosuccinic acid product, the sodium ion solubility of which is less than 0.05 percent, can be obtained; the materials of the route are simple, the synthetic route is simple and reasonable, the conversion rate of reaction is high, the cost is greatly reduced, and moreover, the whole synthetic route is green and environment-friendly, and is suitable for industrial production.

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