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Sulfamethizole

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Name

Sulfamethizole

EINECS 205-641-1
CAS No. 144-82-1 Density 1.562g/cm3
PSA 134.59000 LogP 2.96450
Solubility Insoluble at 6.5, soluble at 7.5 Melting Point 208 - 210 C
Formula C9H10 N4 O2 S2 Boiling Point 504.9°Cat760mmHg
Molecular Weight 270.336 Flash Point 259.1°C
Transport Information 25kgs Appearance white to pale yellow crystalline powder
Safety Moderately toxic by ingestion and subcutaneous routes. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and SOx. See also SULFONATES. Risk Codes R43   
Molecular Structure Molecular Structure of 144-82-1 (SULFAMETHIZOLE) Hazard Symbols
Synonyms

Sulfanilamide,N1-(5-methyl-1,3,4-thiadiazol-2-yl)- (6CI,7CI,8CI); 2-Methyl-5-sulfanilamido-1,3,4-thiadiazole;2-Sulfanilamido-5-methyl-1,3,4-thiadiazole;4-Amino-N-(5-methyl-[1,3,4]thiadiazol-2-yl)benzenesulfonamide;5-Methyl-2-sulfanilamido-1,3,4-thiadiazole; Ayerlucil; Famet; Lucosil;Methazol; Microsul; N-(5-Methyl-1,3,4-thiadiazol-2-yl)-4-aminobenzenesulfonamide;N1-(5-Methyl-1,3,4-thiadiazol-2-yl)sulfanilamide; Renasul; Rufol; Salimol;Sulfamethiazole; Sulfamethizol; Sulfamethizole; Sulfamethylthiadiazole;Sulfapyelon; Sulfstat; Sulfurine; Sulphamethizole; Tetracid; Thidicur;Thiosulfil; Thiosulfil Forte; Ultrasul; Urocydal; Urodiaton; Urolucosil;Urosulfin; VK 53

Article Data 14

Sulfamethizole Synthetic route

349621-24-5

N-(5-methyl-1,3,4-thiadiazol-2-yl)-4-nitrobenzenesulfonamide

144-82-1

sulfamethizole

Conditions
ConditionsYield
With hydrogenchloride; iron In ethanol; water for 3h; Reflux;100%
39719-87-4

N-(4-(N-(5-methyl-1,3,4-thiadiazol-2-yl)sulfamoyl)phenyl)acetamide

144-82-1

sulfamethizole

Conditions
ConditionsYield
Stage #1: N-(4-(N-(5-methyl-1,3,4-thiadiazol-2-yl)sulfamoyl)phenyl)acetamide With hydrogenchloride In water for 0.5h; Reflux;
Stage #2: With sodium carbonate In water
72%
Stage #1: N-(4-(N-(5-methyl-1,3,4-thiadiazol-2-yl)sulfamoyl)phenyl)acetamide With hydrogenchloride In water for 0.5h; Reflux;
Stage #2: With sodium carbonate In water
72%
With hydrogenchloride
With sodium hydroxide
108-33-8

5-methyl-1,3,4-thiadiazol-2-amine

98-74-8

4-Nitrobenzenesulfonyl chloride

144-82-1

sulfamethizole

Conditions
ConditionsYield
anschliessend Erwaermen mit Eisen in wss.-aethanol. HCl;
108-33-8

5-methyl-1,3,4-thiadiazol-2-amine

121-60-8

p-acetylaminobenzenesulfonyl chloride

144-82-1

sulfamethizole

Conditions
ConditionsYield
With pyridine anschliessend Erwaermen mit wss. NaOH;
With hydrogenchloride
2302-95-6

acetaldehyde thiosemicarbazone

121-60-8

p-acetylaminobenzenesulfonyl chloride

144-82-1

sulfamethizole

Conditions
ConditionsYield
With pyridine anschliessend Erwaermen mit Ca32 in wss.-alkal. Loesung;
75-36-5

acetyl chloride

1-acetyl-4--thiosemicarbazide

1-acetyl-4--thiosemicarbazide

144-82-1

sulfamethizole

Conditions
ConditionsYield
anschliessend Hydrolysieren mit Mineralsaeure;
121-60-8

p-acetylaminobenzenesulfonyl chloride

144-82-1

sulfamethizole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: aqueous HCl
View Scheme
Multi-step reaction with 2 steps
1: pyridine / 1 h / 95 °C
2: hydrogenchloride / water / 0.5 h / Reflux
View Scheme
Multi-step reaction with 2 steps
1: pyridine / 0 - 95 °C
2: hydrogenchloride / water / 0.5 h / Reflux
View Scheme
98-74-8

4-Nitrobenzenesulfonyl chloride

144-82-1

sulfamethizole

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: dichloromethane; pyridine / 2 h / 20 °C
2: hydrogenchloride / iron / ethanol; water / 3 h / Reflux
View Scheme
144-82-1

sulfamethizole

15186-48-8

2,3-isopropylidene-glyceraldehyde

4-({[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methylene}amino)-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide

Conditions
ConditionsYield
With toluene-4-sulfonic acid In dimethyl sulfoxide; toluene Condensation;100%
144-82-1

sulfamethizole

methyl 3-formyl-5-iodobenzoate

methyl 3-iodo-5-((4-(N-(5-methyl-1,3,4-thiadiazol-2-yl)sulfamoyl)phenylamino)-methyl)benzoate

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride; acetic acid In dichloromethane at 20℃;99%

Sulfamethizole Chemical Properties

Chemistry informtion about Sulfamethizole (CAS NO.144-82-1) is:
IUPAC Name: 4-Amino-N-(5-Methyl-1,3,4-Thiadiazol-2-Yl)Benzenesulfonamide
Synonyms: 4-Amino-N-[5-Methyl-1,3,4-Thiadiazol-2-Yl]-Benzenesulfonamide ; Labotest-Bb Lt00772293 ; Sulfamethylthiadiazole ; Sulfamethiazole ; Sulfamethizol ; Sulfamethizole ; Sulphamethizole ; N1-(5-Methyl-1,3,4-Thiadiazol-2-Yl)Sulfanilamide
MF: C9H10N4O2S2
MW: 270.33
EINECS: 205-641-1
Density: 1.562 g/cm3
Melting Point: 210 °C
Flash Point: 259.1 °C
Boiling Point: 504.9 °C at 760 mmHg
Vapour Pressure: 2.56E-10 mmHg at 25°C
Enthalpy of Vaporization: 77.44 kJ/mol
Storage temp.:  2-8°C
Merck: 8916
Following is the molecular structure of Sulfamethizole (CAS NO.144-82-1) is:

Sulfamethizole Uses

Sulfamethizole (CAS NO.144-82-1) is used in the prevention and treatment of bacterial infections, diabetes mellitus, edema, hypertension, and gout. Sulfa drug includes:
Topical sulfonamides: sulfacetamide; silver sulfadiazine; mafenide;
Rapidly absorbed and eliminated sulfonamides: sulfisoxazole diolamine; sulfadiazine; sulfamethoxazole;
Hydrophylic sulfonamides: phtalylsulfacetamide; phtalylsulfathiazole; sulfasalazine; sulfaguanidine;
Long lasting sulfonamides: sulfadoxine;
Others: sulfamazole; sulfamazone; sulfametopirazine; sulfametoxypiridazine; sulfametrol; succinylsulfathiazole;

Sulfamethizole Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intramuscular 3668mg/kg (3668mg/kg)   Drugs in Japan Vol. 6, Pg. 388, 1982.
mouse LD50 intraperitoneal 3290mg/kg (3290mg/kg)   Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 9, Pg. 759, 1967.
mouse LD50 intravenous 1820mg/kg (1820mg/kg)   Drugs in Japan Vol. 6, Pg. 388, 1982.
mouse LD50 oral > 10gm/kg (10000mg/kg)   Drugs in Japan Vol. 6, Pg. 388, 1982.
mouse LD50 subcutaneous 1210mg/kg (1210mg/kg)   "Handbook of Analytical Toxicology," Sunshine, I., ed., Cleveland, OH, Chemical Rubber Co., 1969Vol. -, Pg. 111, 1969.
rat LD50 intramuscular 4444mg/kg (4444mg/kg)   Drugs in Japan Vol. 6, Pg. 388, 1982.
rat LD50 intravenous 2710mg/kg (2710mg/kg)   Drugs in Japan Vol. 6, Pg. 388, 1982.
rat LD50 oral 3500mg/kg (3500mg/kg)   Yakugaku Zasshi. Journal of Pharmacy. Vol. 83, Pg. 778, 1963.
rat LD50 subcutaneous > 6560mg/kg (6560mg/kg)   Drugs in Japan Vol. 6, Pg. 388, 1982.

Sulfamethizole Consensus Reports

Reported in EPA TSCA Inventory.

Sulfamethizole Safety Profile

Moderately toxic by ingestion and subcutaneous routes. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and SOx. See also SULFONATES.
Hazard Codes:
IrritantXi
Risk Statements:
R43:May cause sensitization by skin contact.
Safety Statements:
S36/37:Wear suitable protective clothing and gloves.
WGK Germany: 2
RTECS: WP0875000

Sulfamethizole Specification

Sulfamethizole (CAS NO.144-82-1) is a sulfonamide antibiotic. It is a white to pale yellow crystalline powder.And it is insoluble in water. Flammability data is lacking for it. Also it is probably non-flammable.

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