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Acetylsulfanilamide

Acetylsulfanilamide structure

CAS No:
121-61-9
Formula:
C8H10N2O3S
Chemical Name:
Acetylsulfanilamide
Synonyms:
Acetamide,N-[4-(aminosulfonyl)phenyl]-;Acetanilide,4′-sulfamoyl-;N-[4-(Aminosulfonyl)phenyl]acetamide;N4-Acetylsulfanilamide;Neotherapol;p-Sulfamylacetanilide;Erytrin;p-Acetamidobenzenesulfonamide;Benzenesulfonamide,4-(acetylamino)-;Sulfanilamide-N4-acetate;A-319;N-(4-Sulfamoylphenyl)acetamide;p-(Acetylamino)benzenesulfonamide;4′-Sulfamoylacetanilide;Acetylsulfanilamide;N4-Acetsulfanilamide;4-Acetylaminobenzenesulfonamide;4-Acetamidobenzenesulfonamide;p-Sulfamoylacetanilide;N′-Acetylsulphanilamide;NSC 217;NSC 406839
Categories:
Organic Chemistry > Amides

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Description

White to light beige crystalline powder

An anti-bacterial agent that is used topically to treat skin infections and orally for urinary tract infections.

Acetylsulfanilamide Basic Attributes

Molecular Weight：

214.24

Exact Mass：

214.24

EC Number：

204-486-7

UNII：

340484WZ3L

NSC Number：

406839|217

DSSTox ID：

DTXSID4041529

HScode：

2935009090

Characteristics

PSA：

97.6

XLogP3：

2.14650

Density：

1.3844 (rough estimate)

Melting Point：

219.5 °C

Refractive Index：

1.5690 (estimate)

Water Solubility：

slightly soluble

Safety Information

safety instructions：

24/25

RTECS Number：

AE7015000

Marks：

Hazard note：

Irritant

Precautionary statement(s)：

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501

Hazard Statements：

H302

GHS Classification：

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 6 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

MeSH：

Substances capable of killing agents causing urinary tract infections or of preventing them from spreading. (See all compounds classified as Anti-Infective Agents, Urinary.)|Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)|Substances used on humans and other animals that destroy harmful microorganisms or inhibit their activity. They are distinguished from DISINFECTANTS, which are used on inanimate objects. (See all compounds classified as Anti-Infective Agents, Local.)

MeSH Entry Terms：

Acetopt

Acetylsulfanilamide Use and Manufacturing

Uses

p-Sulfamylacetanilide has been used as an inhibitor of mitochondrial isoenzyme carbonic anhydrase V inhibitiors. Vullo, Daniela

Use Classification：

Environmental transformation -> Pesticide transformation products (metabolite, successor)

Agrochemical：

Acetylsulfanilamide is a known environmental transformation product of Asulam.

Computed Properties

Molecular Weight:214.24
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:214.04121336
Monoisotopic Mass:214.04121336
Topological Polar Surface Area:97.6
Heavy Atom Count:14
Complexity:299
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Downstream Products

Sulfamethazine

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4-Acetamidobenzenesulfonamide

CAS No.: 121-61-9

Content: 99.00%

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