Conditions | Yield |
---|---|
With nitric acid bei der Oxydation; |
Conditions | Yield |
---|---|
With chlorosulfonic acid |
chloro-sulfo-acetic acid
sulfoacetic acid
Conditions | Yield |
---|---|
With sodium amalgam |
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With water at 75 - 80℃; bei der elektrolytischen Oxydation an Platin; | |
With sulfuric acid at 75 - 80℃; bei der elektrolytischen Oxydation an PbO2; |
Conditions | Yield |
---|---|
With chromic acid |
(aminoiminomethyl)thioacetic acid ethyl ester
sulfoacetic acid
Conditions | Yield |
---|---|
With water; chlorine |
Conditions | Yield |
---|---|
With dihydrogen peroxide; iron(II) sulfate |
Conditions | Yield |
---|---|
With tetrachloromethane |
Conditions | Yield |
---|---|
With sodium sulfite |
Conditions | Yield |
---|---|
With sulfuric acid | |
With sulfuric acid | |
With sulfur trioxide; oxygen im UV-Licht; |
Conditions | Yield |
---|---|
With sulfur trioxide; 1,2-dichloro-ethane |
Conditions | Yield |
---|---|
With sulfur trioxide | |
With chlorosulfonic acid at 140℃; |
Conditions | Yield |
---|---|
With chlorosulfonic acid unter Kuehlung und Erhitzen des Reaktionsgemisches dann auf 140grad; |
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With silver sulfate at 120℃; |
Conditions | Yield |
---|---|
With water; sodium carbonate; sodium sulfite isolierung aus Bariumsalz; |
acetic acid ethylester sulfonic acid
sulfoacetic acid
Conditions | Yield |
---|---|
saponification; |
acetic acid
A
sulfoacetic acid
B
Acetylsulfat
C
diacetyl sulfate
Conditions | Yield |
---|---|
With sulfur trioxide In liquid sulphur dioxide Product distribution; effect of temperature; |
Conditions | Yield |
---|---|
at 40℃; Rate constant; |
hydrogenchloride
2-ethylamino-thiazol-4-one
A
N-Ethylurea
B
sulfoacetic acid
Conditions | Yield |
---|---|
folgend Eindampfen der von Barium befreiten Loesung; |
acetic anhydride
A
sulfoacetic acid
B
methanedisulfonic acid
C
methanetrisulfonic acid
Conditions | Yield |
---|---|
je nach den Bedingungen wechselnden Mengen; |
hydrogenchloride
water
(16-hydroxy-3β-methoxy-erythrina-1,6-dien-15-yloxysulfonyl)-acetic acid
A
sulfoacetic acid
hydrogenchloride
water
(3β,16-dimethoxy-erythrina-1,6-dien-15-yloxysulfonyl)-acetic acid
A
sulfoacetic acid
Conditions | Yield |
---|---|
at 60℃; unter Ausschluss von Luftfeuchtigkeit und Zersetzen des Reaktionsprodukts mit Eis; bei 4 stuendiger Einw.; |
Conditions | Yield |
---|---|
at 95℃; |
dihydrogen peroxide
mercaptoacetic acid
A
sulfoacetic acid
B
disulfanediyldiacetic acid
C
sulfuric acid
Conditions | Yield |
---|---|
Heating; | 100% |
Conditions | Yield |
---|---|
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
C15H17NO
N-[3-(3-phenoxyphenyl)propyl](sulfo)acetamide
Conditions | Yield |
---|---|
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
sulfoacetic acid
5α,10β,15α,20β-tetrakis(2-aminophenyl)porphyrinatoiron(III) chloride
water
Conditions | Yield |
---|---|
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% |
sulfoacetic acid
Conditions | Yield |
---|---|
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
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
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
sulfoacetic acid
8-Acetyl-1,2,3,4-tetrahydro-5,6-dimethoxy-2-methylisochinolin
Conditions | Yield |
---|---|
24% |
sulfoacetic acid
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
Conditions | Yield |
---|---|
for 0.0833333h; Heating; | 23% |
sulfoacetic acid
Conditions | Yield |
---|---|
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
Conditions | Yield |
---|---|
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
Conditions | Yield |
---|---|
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
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; | 6% |
Conditions | Yield |
---|---|
With sulfuric acid |
Conditions | Yield |
---|---|
With hydrogenchloride; benzene durch anschliessende azeotrope Destillation; |
Conditions | Yield |
---|---|
at 100℃; unter vermindertem Druck; | |
at 100℃; unter vermindertem Druck; |
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
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. |
Reported in EPA TSCA Inventory.
Safety Information of Sulfoacetic acid (CAS NO.123-43-3):
Hazard Codes: C
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 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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