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Sulfisoxazole

CAS No.
127-69-5
Chemical Name:
Sulfisoxazole
Synonyms
SULFAFURAZOLE;SIZ;SULFISOXAZOL;sulphisoxazole;Sosol;vagilia;Sulsoxin;Sulfalar;Gantrisin;SULFAFURAZOL
CBNumber:
CB1495500
Molecular Formula:
C11H13N3O3S
Molecular Weight:
267.3
MDL Number:
MFCD00003150
MOL File:
127-69-5.mol
MSDS File:
SDS
Last updated:2024-11-07 13:31:19

Sulfisoxazole Properties

Melting point 195°C
Boiling point 482.2±55.0 °C(Predicted)
Density 1.3486 (rough estimate)
refractive index 1.6630 (estimate)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility acetone: complete50 mg/ml
pka 5.0(at 25℃)
form Solid
color White to Light Brown
Water Solubility <0.1 g/100 mL at 22.5 ºC
λmax 271nm(MeOH)(lit.)
Merck 14,8952
BRN 6737262
Stability Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 127-69-5(CAS DataBase Reference)
FDA UNII 740T4C525W
ATC code J01EB05,S01AB02
NIST Chemistry Reference Benzenesulfonamide, 4-amino-N-(3,4-dimethyl-5-isoxazolyl)-(127-69-5)
IARC 3 (Vol. 24, Sup 7) 1987
EPA Substance Registry System Sulfisoxazole (127-69-5)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  2
RTECS  WO9100000
HazardClass  IRRITANT
HS Code  29350030
Toxicity LD50 orally in mice: 6800 mg/kg (Seki)
NFPA 704
0
2 0

Sulfisoxazole price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 31739 Sulfisoxazole VETRANAL 127-69-5 250mg $60.7 2024-03-01 Buy
Sigma-Aldrich 1638000 Sulfisoxazole United States Pharmacopeia (USP) Reference Standard 127-69-5 200mg $174.4 2024-03-01 Buy
TCI Chemical U0098 Sulfisoxazole >98.0%(HPLC) 127-69-5 25g $190 2024-03-01 Buy
Sigma-Aldrich S1975000 Sulfafurazole European Pharmacopoeia (EP) Reference Standard 127-69-5 s1975000 $220 2024-03-01 Buy
Cayman Chemical 25980 Sulfisoxazole 127-69-5 1g $37 2024-03-01 Buy
Product number Packaging Price Buy
31739 250mg $60.7 Buy
1638000 200mg $174.4 Buy
U0098 25g $190 Buy
S1975000 s1975000 $220 Buy
25980 1g $37 Buy

Sulfisoxazole Chemical Properties,Uses,Production

Chemical Properties

white to cream powder

Originator

Gantrisin,Roche,US,1949

Uses

Sulfisoxazole is a sulfonamide based antibacterial that exhibits activity against wide spectrum of gram-negative and gram-positive bacterium.

Definition

ChEBI: A sulfonamide antibacterial with an oxazole substituent. It has antibiotic activity against a wide range of gram-negative and gram-positive organisms.

Manufacturing Process

112 parts of 3,4-dimethyl-5-amino-isoxazole were dissolved in a mixture of 100 volume parts of pyridine and 200 volume parts of acetone. The mixture is cooled with cold water and 240 parts p-acetamino-benzene sulfonic acid chloride are added in small portions under stirring at temperatures of below 30°C. The mixture is left standing overnight at 20° to 30°C and then the 5- acetamino-benzene-sulfonylamino-3,4-dimethyl-isoxazole is precipitated by the addition of water. Recrystallized from acetic acid or alcohol it forms small prisms of the melting point 210°C.
100 parts of the 5-acetamino-benzene-sulfonyl-amino-3,4-dimethyl-isoxazole are boiled under reflux with 500 volume parts 15 to 20% aqueous hydrochloric acid for 30 to 45 minutes until all is dissolved. 500 parts crystallized sodium acetate are added and the liquid left cooling for crystallization. The sulfanilamido-3,4-dimethyl-isoxazole is sucked off, washed with water and dried. In the pure state it forms white prisms with the melting point of 193°C.

brand name

Gantrisin (Roche).

Therapeutic Function

Antibacterial

Antimicrobial activity

Like all examined sulfanilamides, this drug is effective in treating infections caused by streptococci, gonococci, pneumococci, staphylococci, and also colon bacillus. However, about 90% of it binds with proteins in the plasma after oral administration, and it diffuses mostly to tissues and tissue fluids, which makes it the drug of choice for many systemic infections. Synonyms of this drug are gantrisin, fultrxin, sulfazin, sulfolar, and others.

General Description

Sulfisoxazole’s plasmahalf-life is 6 hours. This compound is a white, odorless,slightly bitter, crystalline powder. Its pKa is 5.0. At pH 6,this sulfonamide has a water solubility of 350 mg in100 mL, and its acetyl derivative has a solubility of 110 mgin 100 mL of water.Sulfisoxazole possesses the action and the uses of othersulfonamides and is used for infections involving sulfonamide-sensitive bacteria. It is claimed to be effective in thetreatment of Gram-negative urinary infections.

General Description

Odorless white to yellowish crystalline powder. Slightly bitter taste. Acid to litmus.

Air & Water Reactions

May be sensitive to prolonged exposure to air and light. Sensitive to heat. Slightly soluble in water.

Fire Hazard

Flash point data for Sulfisoxazole are not available; however, Sulfisoxazole is probably combustible.

Pharmaceutical Applications

3,4-Dimethyl-5-sulfanilamidoisoxazole. It is highly soluble, even in acid urine. The spectrum and potency are typical of the group. It is well absorbed, achieving a concentration of around 20 mg/L 3–4 h after a 2 g oral dose.
Side effects are those common to other sulfonamides. It is less prone than some other members of the group to cause renal problems. Its principal use is in urinary tract infection, and is present in some ophthalmic preparations.

Biological Activity

A selective ET A endothelin receptor antagonist (IC 50 values are 600 and 2200 nM for ET A and ET B receptors respectively).

Safety Profile

Mildly toxic by ingestion. An experimental teratogen. Questionable carcinogen. Mutation data reported. When heated to decomposition it emits very toxic fumes of SOx and NOx.

Synthesis

Sulfisoxazole, N1 -(3,4-dimethyl-5-isoxazolyl)sulfanilamide (33.1.19), is synthesized by reacting 4-acetylaminobenzenesulfonyl chloride with 5-amino-3, 4-dimethylisoxazol (33.1.17), which is in turn synthesized by heterocyclization of 2-methylacetylacetonitrile with hydroxylamine, and subsequent acidic hydrolysis (hydrochloric acid) of the protective acetyl group in the resulting product (33.1.18).

Synthesis_127-69-5

184644-22-2
127-69-5
Synthesis of Sulfisoxazole from N-(3,4-dimethyl-5-isoxazolyl)-4-nitrobenzenesulfonamide
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View Lastest Price from Sulfisoxazole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sulfisoxazole pictures 2024-11-07 Sulfisoxazole
127-69-5
US $31.00-48.00 / mg 99.98% 10g TargetMol Chemicals Inc.
Sulfisoxazole pictures 2024-11-07 Sulfisoxazole
127-69-5
US $31.00-48.00 / mg 99.98% 10g TargetMol Chemicals Inc.
Sulfisoxazole pictures 2024-04-25 Sulfisoxazole
127-69-5
US $5.00 / kg 1kg 99.92% 50000tons Ouhuang Engineering Materials (Hubei) Co., Ltd
  • Sulfisoxazole pictures
  • Sulfisoxazole
    127-69-5
  • US $31.00-48.00 / mg
  • 99.98%
  • TargetMol Chemicals Inc.
  • Sulfisoxazole pictures
  • Sulfisoxazole
    127-69-5
  • US $31.00-48.00 / mg
  • 99.98%
  • TargetMol Chemicals Inc.
  • Sulfisoxazole pictures
  • Sulfisoxazole
    127-69-5
  • US $5.00 / kg
  • 99.92%
  • Ouhuang Engineering Materials (Hubei) Co., Ltd
LABOTEST-BB LT00053357 AKOS B020058 sulfanilamide,n(sup1)-(3,4-dimethyl-5-isoxazolyl) Sulfapolar Sulfasan Sulfasol Sulfazin Sulfisin Sulfisonazole Sulfisoxasole Sulfisoxazole dialamine Sulfizin Sulfizol Sulfizole Sulfoxol Suloxsol Sulphadimethylisoxazole Sulphafuraz Sulphafurazol Sulphafurazolum Sulphaisoxazole Sulphisoxazol Sulphofurazole Thiasin tl-azole Chemouag component of Azo Gantrisin component of Azo-Sulfizin Cosoxazole Dorsulfan Dorsulfan Warthausen dorsulfanwarthausen Entusil Entusul Ganda Gantrisine Gantrisona Gantrosan G-sox Isoxamin J-Sul Koro-sulf n(1)-(3,4-dimethyl-5-isoxazolyl)-sulfanilamid N'-(3,4)Dimethylisoxazol-5-yl-sulphanilamide n(sup1)-(3,4-dimethyl-5-isoxazolyl)-sulfanilamid N(Sup1)-(3,4-Dimethyl-5-isoxazolyl)sulfanilamide n(sup1)-(3,4-dimethyl-5-isoxazolyl)sulphanilamide 3,4-Dimethyl-5-sulfonamidoisoxazole 3,4-Dimethyl-5-sulphanilamidoisoxazole 3,4-Dimethyl-5-sulphonamidoisoxazole 3,4-Dimethylisoxale-5-sulfanilamide 3,4-dimethyl-5-sulfanilamidoisoxazole 3,4-dimethylisoaxazole-5-sulfanilimide SULFISOXAZOLE TIMTEC-BB SBB007602 N1-(3,4-DIMETHYL-5-ISOXAZOLYL)SULFANILAMIDE Sulfisoxazole (200 mg) 4-Amino-N-(3,4-dimethylisoxazol-5-yl)-benzenesulfonamide