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Sulfanilamide, 98%
CAS: 63-74-1 | C6H8N2O2S | 172.202 g/mol
$75.55 - $630.22
Identifiants chimiques
| CAS | 63-74-1 |
|---|---|
| Molecular Formula | C6H8N2O2S |
| Molecular Weight (g/mol) | 172.202 |
| MDL Number | MFCD00007939 |
| InChI Key | FDDDEECHVMSUSB-UHFFFAOYSA-N |
| Synonym | sulfanilamide, sulphanilamide, sulfamine, sulphonamide, p-aminobenzenesulfonamide, sulfonylamide, sulfonamide, p-aminobenzenesulfamide, bacteramid, streptasol |
| PubChem CID | 5333 |
| ChEBI | CHEBI:45373 |
| IUPAC Name | 4-aminobenzenesulfonamide |
| SMILES | C1=CC(=CC=C1N)S(=O)(=O)N |
| Numéro de catalogue | Numéro du manufacturier. | Quantity | Prix | Quantité | |||||
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| Numéro de catalogue | Numéro du manufacturier. | Quantity | Prix | Quantité | |||||
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AAA1300122
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Thermo Scientific Chemicals
A1300122 |
100 g |
chaque for $75.55
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AAA1300136
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Thermo Scientific Chemicals
A1300136 |
500 g |
chaque for $167.53
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Connectez-vous ou enregistrez-vous pour vérifier votre prix et la disponibilité.
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AAA130010E
|
Thermo Scientific Chemicals
A130010E |
2500 g |
chaque for $630.22
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Connectez-vous ou enregistrez-vous pour vérifier votre prix et la disponibilité.
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Description
Sulfonamide antibacterial Sulfanilamide is an antibacterial and used in the treatment of vaginal yeast infections. It is a competitive inhibitor of dihydropteroate synthestase to block the synthesis of folic acid. It serves as an intermediate for the preparation of 2,6-disubstituted anilines by electrophilic substitution followed by removal of the sulfonamide blocking group by desulfonation with sulfuric acid.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsSulfonamide antibacterial Sulfanilamide is an antibacterial and used in the treatment of vaginal yeast infections. It is a competitive inhibitor of dihydropteroate synthestase to block the synthesis of folic acid. It serves as an intermediate for the preparation of 2,6-disubstituted anilines by electrophilic substitution followed by removal of the sulfonamide blocking group by desulfonation with sulfuric acid.
Solubility
Soluble in water, acetone, ethanol, glycerol, propylene glycol and hydrochloric acid. Insoluble in chloroform, ether, benzene and petroleum ether.
Notes
Incompatible with strong oxidizing agents.
Identifiants chimiques
| 63-74-1 | |
| 172.202 | |
| FDDDEECHVMSUSB-UHFFFAOYSA-N | |
| 5333 | |
| 4-aminobenzenesulfonamide |
| C6H8N2O2S | |
| MFCD00007939 | |
| sulfanilamide, sulphanilamide, sulfamine, sulphonamide, p-aminobenzenesulfonamide, sulfonylamide, sulfonamide, p-aminobenzenesulfamide, bacteramid, streptasol | |
| CHEBI:45373 | |
| C1=CC(=CC=C1N)S(=O)(=O)N |
Spécifications
| 63-74-1 | |
| 1.08 | |
| MFCD00007939 | |
| 511852 | |
| sulfanilamide, sulphanilamide, sulfamine, sulphonamide, p-aminobenzenesulfonamide, sulfonylamide, sulfonamide, p-aminobenzenesulfamide, bacteramid, streptasol | |
| FDDDEECHVMSUSB-UHFFFAOYSA-N | |
| 4-aminobenzenesulfonamide | |
| 5333 | |
| 172.21 | |
| Sulfanilamide |
| 163°C to 168°C | |
| C6H8N2O2S | |
| 100 g | |
| 14,8925 | |
| Soluble in water,acetone,ethanol,glycerol,propylene glycol and hydrochloric acid. Insoluble in chloroform,ether,benzene and petroleum ether. | |
| C1=CC(=CC=C1N)S(=O)(=O)N | |
| 172.202 | |
| CHEBI:45373 | |
| 98% |
Sécurité et manipulation
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
missing translation for 'einecsNumber' : 200-563-4
missing translation for 'rtecsNumber' : WO8400000
missing translation for 'tsca' : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only