Product Name

  • Name

    SULFOACETIC ACID

  • EINECS 204-627-2
  • CAS No. 123-43-3
  • Article Data79
  • CAS DataBase
  • Density 1.875g/cm3
  • Solubility 103.7g/L at 25℃
  • Melting Point 81-88 °C(lit.)
  • Formula C2H4 O5 S
  • Boiling Point °Cat760mmHg
  • Molecular Weight 140.117
  • Flash Point °C
  • Transport Information
  • Appearance
  • Safety Moderately toxic by ingestion and skin contact. A skin and severe eye irritant. When heated to decomposition it emits toxic fumes of SOx.
  • Risk Codes 34-36/37
  • Molecular Structure Molecular Structure of 123-43-3 (SULFOACETIC ACID)
  • Hazard Symbols
  • Synonyms Aceticacid, sulfo- (6CI,7CI,8CI,9CI);Sulfoacetic acid;Sulfoethanoic acid;
  • PSA 100.05000
  • LogP 0.03960

Synthetic route

thirane
420-12-2

thirane

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With nitric acid bei der Oxydation;
acetamide
60-35-5

acetamide

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With chlorosulfonic acid
tetrachloromethane
56-23-5

tetrachloromethane

acetoxysulfonic acid
2308-54-5

acetoxysulfonic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

chloro-sulfo-acetic acid
69406-58-2

chloro-sulfo-acetic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With sodium amalgam
sulfosuccinic acid
5138-18-1

sulfosuccinic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With potassium hydroxide
ethanesulfonic acid
594-45-6

ethanesulfonic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With water at 75 - 80℃; bei der elektrolytischen Oxydation an Platin;
With sulfuric acid at 75 - 80℃; bei der elektrolytischen Oxydation an PbO2;
2-hydroxyethanesulfonic acid
107-36-8

2-hydroxyethanesulfonic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With chromic acid
(aminoiminomethyl)thioacetic acid ethyl ester
24523-90-8

(aminoiminomethyl)thioacetic acid ethyl ester

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With water; chlorine
disulfanediyldiacetic acid
505-73-7

disulfanediyldiacetic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With dihydrogen peroxide; iron(II) sulfate
acetoxysulfonic acid
2308-54-5

acetoxysulfonic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With tetrachloromethane
sodium monochloroacetic acid
3926-62-3

sodium monochloroacetic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With sodium sulfite
acetic anhydride
108-24-7

acetic anhydride

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With sulfuric acid
With sulfuric acid
With sulfur trioxide; oxygen im UV-Licht;
(formylmethyl)mercury chloride
5321-77-7

(formylmethyl)mercury chloride

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With sulfur trioxide; 1,2-dichloro-ethane
acetic acid
64-19-7

acetic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With sulfur trioxide
With chlorosulfonic acid at 140℃;
acetic acid
64-19-7

acetic acid

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

methanedisulfonic acid
503-40-2

methanedisulfonic acid

Conditions
ConditionsYield
With chlorosulfonic acid unter Kuehlung und Erhitzen des Reaktionsgemisches dann auf 140grad;
mercaptoacetic acid
68-11-1

mercaptoacetic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With nitric acid
acetyl chloride
75-36-5

acetyl chloride

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With silver sulfate at 120℃;
chloroacetic acid
79-11-8

chloroacetic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
With water; sodium carbonate; sodium sulfite isolierung aus Bariumsalz;
acetic acid ethylester sulfonic acid
89124-45-8

acetic acid ethylester sulfonic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
saponification;
acetic acid
64-19-7

acetic acid

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

Acetylsulfat
100151-21-1

Acetylsulfat

C

diacetyl sulfate
2480-60-6

diacetyl sulfate

D

acetyl disulphate (keto-form)

acetyl disulphate (keto-form)

Conditions
ConditionsYield
With sulfur trioxide In liquid sulphur dioxide Product distribution; effect of temperature;
sulfuric acid
7664-93-9

sulfuric acid

acetic anhydride
108-24-7

acetic anhydride

acetic acid
64-19-7

acetic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
at 40℃; Rate constant;
hydrogenchloride
7647-01-0

hydrogenchloride

2-ethylamino-thiazol-4-one
37704-67-9

2-ethylamino-thiazol-4-one

barium chlorate

barium chlorate

A

N-Ethylurea
625-52-5

N-Ethylurea

B

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
folgend Eindampfen der von Barium befreiten Loesung;
acetic anhydride
108-24-7

acetic anhydride

oleum

oleum

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

methanedisulfonic acid
503-40-2

methanedisulfonic acid

C

methanetrisulfonic acid
54322-33-7

methanetrisulfonic acid

Conditions
ConditionsYield
je nach den Bedingungen wechselnden Mengen;
thirane
420-12-2

thirane

nitric acid
7697-37-2

nitric acid

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

2-carboxymethylsulfanyl-ethane-sulfonic acid-(1)

2-carboxymethylsulfanyl-ethane-sulfonic acid-(1)

hydrogenchloride
7647-01-0

hydrogenchloride

water
7732-18-5

water

(16-hydroxy-3β-methoxy-erythrina-1,6-dien-15-yloxysulfonyl)-acetic acid
466-71-7

(16-hydroxy-3β-methoxy-erythrina-1,6-dien-15-yloxysulfonyl)-acetic acid

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

erysopine

erysopine

hydrogenchloride
7647-01-0

hydrogenchloride

water
7732-18-5

water

(3β,16-dimethoxy-erythrina-1,6-dien-15-yloxysulfonyl)-acetic acid
466-79-5

(3β,16-dimethoxy-erythrina-1,6-dien-15-yloxysulfonyl)-acetic acid

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

erysovine

erysovine

chlorosulfonic acid
7790-94-5

chlorosulfonic acid

acetic acid
64-19-7

acetic acid

sulfoacetic acid
123-43-3

sulfoacetic acid

chlorosulfonic acid
7790-94-5

chlorosulfonic acid

acetyl chloride
75-36-5

acetyl chloride

sulfoacetic acid
123-43-3

sulfoacetic acid

Conditions
ConditionsYield
at 60℃; unter Ausschluss von Luftfeuchtigkeit und Zersetzen des Reaktionsprodukts mit Eis; bei 4 stuendiger Einw.;
acetic acid
64-19-7

acetic acid

oleum

oleum

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

methanetrisulfonic acid
54322-33-7

methanetrisulfonic acid

Conditions
ConditionsYield
at 95℃;
dihydrogen peroxide
7722-84-1

dihydrogen peroxide

mercaptoacetic acid
68-11-1

mercaptoacetic acid

A

sulfoacetic acid
123-43-3

sulfoacetic acid

B

disulfanediyldiacetic acid
505-73-7

disulfanediyldiacetic acid

C

sulfuric acid
7664-93-9

sulfuric acid

ethanol
64-17-5

ethanol

sulfoacetic acid
123-43-3

sulfoacetic acid

acetic acid ethylester sulfonic acid
89124-45-8

acetic acid ethylester sulfonic acid

Conditions
ConditionsYield
Heating;100%
sulfoacetic acid
123-43-3

sulfoacetic acid

3,5-dibromo-4-methylaniline
13194-73-5

3,5-dibromo-4-methylaniline

C9H9Br2NO4S

C9H9Br2NO4S

Conditions
ConditionsYield
With dmap; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 2h;99%
sulfoacetic acid
123-43-3

sulfoacetic acid

C15H17NO
1057671-89-2

C15H17NO

N-[3-(3-phenoxyphenyl)propyl](sulfo)acetamide
1160847-68-6

N-[3-(3-phenoxyphenyl)propyl](sulfo)acetamide

Conditions
ConditionsYield
Stage #1: sulfoacetic acid; C15H17NO With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 2h;
Stage #2: In methanol
85%
methanol
67-56-1

methanol

sulfoacetic acid
123-43-3

sulfoacetic acid

5α,10β,15α,20β-tetrakis(2-aminophenyl)porphyrinatoiron(III) chloride
220457-32-9, 743422-30-2, 97775-27-4

5α,10β,15α,20β-tetrakis(2-aminophenyl)porphyrinatoiron(III) chloride

water
7732-18-5

water

sodium 5α,10β,15α,20β-tetrakis(2-(sulfonatoacetamido)phenyl)porphyrinatoiron(III) hydroxide hexahydrate*3(methanol)

sodium 5α,10β,15α,20β-tetrakis(2-(sulfonatoacetamido)phenyl)porphyrinatoiron(III) hydroxide hexahydrate*3(methanol)

Conditions
ConditionsYield
With isobutyl chlorocarbonate; triethyl amine In dichloromethane sulfoacetic acid added to soln. of isobutyl carbonate and Et3N; stirred at room temp. for 30 min; soln. of Fe compd. in CH2Cl2 added; stirred atroom temp. for 24 h; evapd. to dryness; dissolved in CHCl3; org. layer extd. (aq. NaOH); aq. layer washed (CHCl3); soln. evapd. to dryness; dissolved in EtOH; filtered; filtrate evapd.; purified by chromy. (Cosmosil 75C18-OPN, MeOH-H2O); evapd. to dryness;recrystd. (MeOH-ether); elem. anal.;79%
dinitrato(1,2-diaminoethane)platinum(II)

dinitrato(1,2-diaminoethane)platinum(II)

sulfoacetic acid
123-43-3

sulfoacetic acid

di-μ-sulfoacetato-bis(1,2-diaminoethane)platinum(II) trihydrate

di-μ-sulfoacetato-bis(1,2-diaminoethane)platinum(II) trihydrate

Conditions
ConditionsYield
In water Passing a sol. of Pt-complex through a column of an anion-exchange resin (Diaion SA10AOH), passing of an addnl. amount of H2O through the column, addn. of sulfoacetic acid to the eluate.; Concg. filtn., elem. anal.;68%
sulfoacetic acid
123-43-3

sulfoacetic acid

(S)-N-(2-(2-(2-aminoethoxy)ethoxy)ethyl)-2-(4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)acetamide

(S)-N-(2-(2-(2-aminoethoxy)ethoxy)ethyl)-2-(4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)acetamide

(S)-14-(4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-2,13-dioxo-6,9-dioxa-3,12-diazatetradecane-1-sulfonic acid

(S)-14-(4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl)-2,13-dioxo-6,9-dioxa-3,12-diazatetradecane-1-sulfonic acid

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; ((3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) In N,N-dimethyl-formamide at 20℃; for 16h;62%
sulfoacetic acid
123-43-3

sulfoacetic acid

C20H39NO4

C20H39NO4

C22H40NO8S(1-)*Na(1+)

C22H40NO8S(1-)*Na(1+)

Conditions
ConditionsYield
Stage #1: C20H39NO4 With triethylamine In tetrahydrofuran
Stage #2: sulfoacetic acid With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride In chloroform for 18h; Cooling;
Stage #3: With sodium hydrogencarbonate In chloroform
27.1%
sulfoacetic acid
123-43-3

sulfoacetic acid

C22H43NO4

C22H43NO4

C24H44NO8S(1-)*Na(1+)

C24H44NO8S(1-)*Na(1+)

Conditions
ConditionsYield
Stage #1: C22H43NO4 With triethylamine In tetrahydrofuran
Stage #2: sulfoacetic acid With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride In chloroform for 18h; Cooling;
Stage #3: With sodium hydrogencarbonate In chloroform
27.1%
sulfoacetic acid
123-43-3

sulfoacetic acid

C24H47NO4

C24H47NO4

C26H48NO8S(1-)*Na(1+)

C26H48NO8S(1-)*Na(1+)

Conditions
ConditionsYield
Stage #1: C24H47NO4 With triethylamine In tetrahydrofuran
Stage #2: sulfoacetic acid With bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride In chloroform for 18h; Cooling;
Stage #3: With sodium hydrogencarbonate In chloroform
27.1%
1,2,3,4-Tetrahydro-5,6-dimethoxy-2-methylisochinolin
87664-82-2

1,2,3,4-Tetrahydro-5,6-dimethoxy-2-methylisochinolin

sulfoacetic acid
123-43-3

sulfoacetic acid

8-Acetyl-1,2,3,4-tetrahydro-5,6-dimethoxy-2-methylisochinolin
87664-92-4

8-Acetyl-1,2,3,4-tetrahydro-5,6-dimethoxy-2-methylisochinolin

Conditions
ConditionsYield
24%
sulfoacetic acid
123-43-3

sulfoacetic acid

1,2-Dimethoxy-5,7,8,9,9a,10-hexahydro-pyrrolo<1,2-b>isochinolin
87664-46-8

1,2-Dimethoxy-5,7,8,9,9a,10-hexahydro-pyrrolo<1,2-b>isochinolin

4-Acety-1,2-dimethoxy-5,7,8,9,9a,10-hexahydro-pyrrolo<1,2-b>isochinolin
87664-49-1

4-Acety-1,2-dimethoxy-5,7,8,9,9a,10-hexahydro-pyrrolo<1,2-b>isochinolin

Conditions
ConditionsYield
for 0.0833333h; Heating;23%
sulfoacetic acid
123-43-3

sulfoacetic acid

(E)-N-(4-(1-(3-((2-(2-(2-aminoethoxy)ethoxy)acetamido)methyl)benzoyl)piperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamide bis-2,2,2-trifluoroacetate

(E)-N-(4-(1-(3-((2-(2-(2-aminoethoxy)ethoxy)acetamido)methyl)benzoyl)piperidin-4-yl)butyl)-3-(pyridin-3-yl)acrylamide bis-2,2,2-trifluoroacetate

(E)-3,12-dioxo-1-(3-(4-(4-(3-(pyridin-3-yl)acrylamido)butyl)piperidine-1-carbonyl)phenyl)-5,8-dioxa-2,11-diazatridecane-13-sulfonic acid 2,2,2-trifluoroacetate

(E)-3,12-dioxo-1-(3-(4-(4-(3-(pyridin-3-yl)acrylamido)butyl)piperidine-1-carbonyl)phenyl)-5,8-dioxa-2,11-diazatridecane-13-sulfonic acid 2,2,2-trifluoroacetate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; ((3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) In N,N-dimethyl-formamide at 20℃; for 16h;20.2%
sulfoacetic acid
123-43-3

sulfoacetic acid

N-(2-(2-(2-aminoethoxy)ethoxy)ethyl)-2-((3-(2-(2-hydroxy-3-(isopropylamino)propoxy)phenyl)propyl)thio)acetamide bis-2,2,2-trifluoroacetate

N-(2-(2-(2-aminoethoxy)ethoxy)ethyl)-2-((3-(2-(2-hydroxy-3-(isopropylamino)propoxy)phenyl)propyl)thio)acetamide bis-2,2,2-trifluoroacetate

C25H43N3O9S2*C2HF3O2

C25H43N3O9S2*C2HF3O2

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 16h;17.2%
sulfoacetic acid
123-43-3

sulfoacetic acid

4-(3-(4-(2-(2-(2-aminoethoxy)ethoxy)acetyl)piperazine-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-one 2,2,2-trifluoroacetate

4-(3-(4-(2-(2-(2-aminoethoxy)ethoxy)acetyl)piperazine-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-one 2,2,2-trifluoroacetate

2-((2-(2-(2-(4-(2-fluoro-5-((4-oxo-3,4-dihydrophthalazin-1-yl)methyl)benzoyl)piperazin-1-yl)-2-oxoethoxy)ethoxy)ethyl)amino)-2-oxoethane-1-sulfonic acid

2-((2-(2-(2-(4-(2-fluoro-5-((4-oxo-3,4-dihydrophthalazin-1-yl)methyl)benzoyl)piperazin-1-yl)-2-oxoethoxy)ethoxy)ethyl)amino)-2-oxoethane-1-sulfonic acid

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide at 20℃; for 16h;7.9%
sulfoacetic acid
123-43-3

sulfoacetic acid

(S)-N-(2-(2-aminoethoxy)ethyl)-5-(3-chloro-2-methyl-N-(1-(3-(3-methylpyridin-4-yl)phenyl)ethyl)phenylsulfonamido)pentanamide hydrochloric acid

(S)-N-(2-(2-aminoethoxy)ethyl)-5-(3-chloro-2-methyl-N-(1-(3-(3-methylpyridin-4-yl)phenyl)ethyl)phenylsulfonamido)pentanamide hydrochloric acid

(S)-15-((3-chloro-2-methylphenyl)sulfonyl)-16-(3-(3-methylpyridin-4-yl)phenyl)-2,10- dioxo-6-oxa-3,9,15-triazaheptadecane-1-sulfonic acid

(S)-15-((3-chloro-2-methylphenyl)sulfonyl)-16-(3-(3-methylpyridin-4-yl)phenyl)-2,10- dioxo-6-oxa-3,9,15-triazaheptadecane-1-sulfonic acid

Conditions
ConditionsYield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃;6%
acetamide
60-35-5

acetamide

sulfoacetic acid
123-43-3

sulfoacetic acid

methanedisulfonic acid
503-40-2

methanedisulfonic acid

Conditions
ConditionsYield
With sulfuric acid
methanol
67-56-1

methanol

sulfoacetic acid
123-43-3

sulfoacetic acid

methoxycarbonyl-methanesulfonic acid
63409-57-4

methoxycarbonyl-methanesulfonic acid

Conditions
ConditionsYield
With hydrogenchloride; benzene durch anschliessende azeotrope Destillation;
1-octadecanol
112-92-5

1-octadecanol

sulfoacetic acid
123-43-3

sulfoacetic acid

octadecyloxycarbonyl-methanesulfonic acid

octadecyloxycarbonyl-methanesulfonic acid

Conditions
ConditionsYield
at 100℃; unter vermindertem Druck;
at 100℃; unter vermindertem Druck;

Sulfoacetic acid Chemical Properties

Molecular Structure of Sulfoacetic acid (CAS NO.123-43-3):

EINECS: 204-627-2
IUPAC Name: 2-Sulfoacetic acid 
Molecular Formula: C2H4O5S
Molecular Weight: 140.115160 g/mol
XLogP3-AA: -1.3
H-Bond Donor: 2
H-Bond Acceptor: 5
Canonical SMILES: C(C(=O)O)S(=O)(=O)O
InChI: InChI=1S/C2H4O5S/c3-2(4)1-8(5,6)7/h1H2,(H,3,4)(H,5,6,7)
InChIKey: AGGIJOLULBJGTQ-UHFFFAOYSA-N
Index of Refraction: 1.536
Molar Refractivity: 23.3 cm3
Molar Volume: 74.7 cm3
Surface Tension: 95.2 dyne/cm
Density: 1.875 g/cm3
Melting Point: 81-88 °C(lit.)
Water Solubility: 1.037e+005 mg/L at 25 °C
BRN: 1764390

Sulfoacetic acid Toxicity Data With Reference

1.    

skn-rbt 20 mg/24H MOD

    85JCAE    Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,1051.
2.    

eye-rbt 250 µg/24H SEV

    85JCAE    Prehled Prumyslove Toxikologie; Organicke Latky Marhold, J.,Prague, Czechoslovakia.: Avicenum,1986,1051.
3.    

orl-rat LD50:3160 mg/kg

    JIHTAB    Journal of Industrial Hygiene and Toxicology. 31 (1949),60.
4.    

skn-rbt LD50:1570 mg/kg

    JIHTAB    Journal of Industrial Hygiene and Toxicology. 31 (1949),60.

Sulfoacetic acid Consensus Reports

Reported in EPA TSCA Inventory.

Sulfoacetic acid Safety Profile

Safety Information of Sulfoacetic acid (CAS NO.123-43-3):
Hazard Codes: C Corrosive
Risk Statements: 34-36/37
R34:Causes burns
R36/37:Irritating to eyes and respiratory system
Safety Statements: 26-27-28-36/37/39-45
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
S27:Take off immediately all contaminated clothing
S28:After contact with skin, wash immediately with plenty of soap-suds
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
RIDADR: UN 3261 8/PG 2
WGK Germany: 3
RTECS: AJ4900000
HazardClass: 8
PackingGroup: III
Moderately toxic by ingestion and skin contact. A skin and severe eye irritant. When heated to decomposition it emits toxic fumes of SOx.

Sulfoacetic acid Specification

  Sulfoacetic acid with CAS registry number of 123-43-3 is also known as 4-04-00-00102 (Beilstein Handbook Reference) ; AI3-28536 ; Acetic acid, sulfo- ; Acetic acid, 2-sulfo- ; HSDB 2706 ; Kyselina sulfooctova ; Kyselina sulfooctova [Czech] ; Sulfoethanoic acid ; Sulphoacetic acid .

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