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CAS NO.144-80-9
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Product information
N-((4-Aminophenyl)sulfonyl)acetamide Basic information |
Product Name: | N-((4-Aminophenyl)sulfonyl)acetamide |
Synonyms: | AKOS BBB/023;LABOTEST-BB LT00053160;A-500;Acetamide, N-[(4-aminophenyl)sulfonyl]-;Acetamide, N-sulfanilyl-;Acetocid;Acetosulfamin;Acetosulfamine |
CAS: | 144-80-9 |
MF: | C8H10N2O3S |
MW: | 214.24 |
EINECS: | 205-640-6 |
Product Categories: | API intermediates;Pharmaceutical intermediate;Others |
Mol File: | 144-80-9.mol |
N-((4-Aminophenyl)sulfonyl)acetamide Chemical Properties |
mp | 182-184 °C |
storage temp. | 0-6°C |
Water Solubility | <0.01 g/100 mL at 16 ºC |
Merck | 14,8899 |
BRN | 981718 |
Stability: | Stable. Incompatible with strong oxidizing agents, strong bases, strong reducing agents, strong acids. |
CAS DataBase Reference | 144-80-9(CAS DataBase Reference) |
NIST Chemistry Reference | N-(p-Aminobenzenesulfonyl)acetamide(144-80-9) |
EPA Substance Registry System | Acetamide, N-[(4-aminophenyl)sulfonyl]- (144-80-9) |
Safety Information |
Hazard Codes | Xi |
Risk Statements | 20/21/22-36/37/38 |
Safety Statements | 22-24/25-36-26 |
RIDADR | 3249 |
WGK Germany | 2 |
RTECS | AC8450000 |
HazardClass | 6.1(b) |
PackingGroup | III |
MSDS Information |
Provider | Language |
---|---|
N-((4-Aminophenyl)sulfonyl)acetamide | English |
SigmaAldrich | English |
ALFA | English |
N-((4-Aminophenyl)sulfonyl)acetamide Usage And Synthesis |
Chemical Properties | white crystalline powder |
Usage | Sulfacetamide is an antibiotic used for the treatment of skin infections and urinary tract infections. Sulfacetamide is also used to treat acne and seborrheic dermatitis. Sulfacetamide was investigate d for potential anti-inflammatory properties |
General Description | White powder. |
Air & Water Reactions | Insoluble in water. |
Reactivity Profile | N-((4-Aminophenyl)sulfonyl)acetamide is an amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generate mixed oxides of nitrogen (NOx) |
Fire Hazard |
Flash point data for N-((4-Aminophenyl)sulfonyl)acetamide are not available. N-((4-Aminophenyl)sulfonyl)acetamide is probably combustible.
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