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Sulfamethoxypyridazine

CAS No.
80-35-3
Chemical Name:
Sulfamethoxypyridazine
Synonyms
Sulphamethoxypyridazine;Sulfamethoxypyridazine-d3;SMPZ;Paramid;Sulfametoxipiridazine;6-Sulfanilamido-3-methoxypyridazine;N1-(6-Methoxy-3-pyridazinyl)sulfanilamide;Durox;Kinex;Kynex
CBNumber:
CB1107025
Molecular Formula:
C11H12N4O3S
Molecular Weight:
280.3
MDL Number:
MFCD00057372
MOL File:
80-35-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 23:04:08

Sulfamethoxypyridazine Properties

Melting point 182-183°
Boiling point 564.9±60.0 °C(Predicted)
Density 1.3936 (rough estimate)
refractive index 1.6200 (estimate)
storage temp. 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form Crystalline Powder
pka 6.7(at 25℃)
color White to yellow
Water Solubility 579.5mg/L(25 ºC)
Merck 14,8919
BRN 277076
Major Application forensics and toxicology
pharmaceutical (small molecule)
InChI InChI=1S/C11H12N4O3S/c1-18-11-7-6-10(13-14-11)15-19(16,17)9-4-2-8(12)3-5-9/h2-7H,12H2,1H3,(H,13,15)
InChIKey VLYWMPOKSSWJAL-UHFFFAOYSA-N
SMILES C1(S(NC2=NN=C(OC)C=C2)(=O)=O)=CC=C(N)C=C1
CAS DataBase Reference 80-35-3(CAS DataBase Reference)
FDA UNII T034E4NS2Z
ATC code J01ED05
NIST Chemistry Reference Pyridazine, sulfamethoxy-(80-35-3)
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)
GHS08
Signal word  Danger
Hazard statements  H317-H334
Precautionary statements  P261-P272-P280-P284-P302+P352-P333+P313
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  37/38-41
Safety Statements  26-39
WGK Germany  2
RTECS  WP0400000
10
HS Code  29350090
Storage Class 11 - Combustible Solids
Hazard Classifications Resp. Sens. 1
Skin Sens. 1
Toxicity LD50 orally in mice: 1750 mg/kg, (Seki)
NFPA 704
0
2 0

Sulfamethoxypyridazine price More Price(44)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S2150000 Sulfamethoxypyridazine European Pharmacopoeia (EP) Reference Standard 80-35-3 50 mg $164 2026-04-30 Buy
Sigma-Aldrich 46858 Sulfamethoxypyridazine VETRANAL?, analytical standard 80-35-3 250mg $74.8 2026-04-30 Buy
TCI Chemical S0591 Sulfamethoxypyridazine >98.0%(HPLC)(T) 80-35-3 5g $30 2026-04-30 Buy
TCI Chemical S0591 Sulfamethoxypyridazine >98.0%(HPLC)(T) 80-35-3 25g $81 2026-04-30 Buy
Cayman Chemical 21875 Sulfamethoxypyridazine ≥95% 80-35-3 5g $36 2026-04-30 Buy
Product number Packaging Price Buy
S2150000 50 mg $164 Buy
46858 250mg $74.8 Buy
S0591 5g $30 Buy
S0591 25g $81 Buy
21875 5g $36 Buy

Sulfamethoxypyridazine Chemical Properties, Uses, Production

Chemical Properties

White or slightly yellow crystalline powder; odorless, bitter taste; discolored when exposed to light. The product is slightly soluble in acetone, very slightly soluble in ethanol, almost insoluble in water; easily soluble in dilute hydrochloric acid or alkali hydroxide solution.

Uses

Sulfamethoxypyridazine is a long-acting sulfonamide antibiotic with anti-inflammatory and antibacterial effects, mainly used for streptococcus, staphylococcus, Escherichia coli and other infections, especially for urinary tract infections.

Application

Sulfamethoxypyridazine may be used as a reference standard for the determination of sulfamethoxypyridazine in pharmaceutical formulations by liquid chromatography method.

Indications

This drug possesses antibacterial activity with respect to a few cocci and colon bacillus. It is a long-lasting drug. It is used for treating pneumonia, bronchitis, tonsillitis, purulent otitis and meningitis, purulent infections of the urinary tract, dysentery, and others. Synonyms of this drug are sulfapyridazine, sufalex, retasulfin, and many others.

Definition

ChEBI: Sulfamethoxypyridazine is a sulfonamide consisting of pyridazine having a methoxy substituent at the 6-position and a 4-aminobenzenesulfonamido group at the 3-position. It has a role as an antiinfective agent, an EC 2.5.1.15 (dihydropteroate synthase) inhibitor and a drug allergen. It is a member of pyridazines, a sulfonamide and a sulfonamide antibiotic. It derives from a sulfanilamide.

brand name

Amidin;Aseptilex;Asey-sulfa;Bimalong;Biocorn;Bio-cron;Bio-pectodil;Davosin suspension;Deltavagin;Desulfon;Durasul jarabe;Elix;Ensulfa;Eusulfa;Exazole;Farinffnicol;Fercasulf;Hesse-sulfon;Ketiak;Kynex acetyl;Lentosulfa;Linder;Logisul jarabe;Longamid;Longisul;Metamit;Metazina;Metuzina;Minikel;Novosulfin;Pirasulfon;Ralenta;Rotardon;S.d.m.;Septotryl;Smop;Sulamin;Sulfa spirig;Sulfabon;Sulfadazina;Sulfadepot;Sulfadin;Sulfadurazin;Sulfaintensa;Sulfakeyn;Sulfametopyridazin;Sulfamizina;Sulfamyd;Sulfapyrazin;Sulfatar;Sulfocidan;Sulfonamid;Sulforetent;Sulfo-rit;Unisulfa dulcis;Uroplex;Velaten;Volocid;Vtg 44.

World Health Organization (WHO)

Sulfamethoxypyridazine, a sulfonamide anti-infective agent, was introduced in 1957 for the treatment of bacterial infections. The importance of sulfonamides has subsequently decreased as a result of increasing bacterial resistance and their replacement by antibiotics which are generally more active and less toxic. The sulfonamides are known to cause serious adverse effects such as renal toxicity, sometimes fatal exfoliative dermatitis and erythema multiforma and dangerous adverse reactions affecting blood formation such as agranulocytosis and haemolytic or aplastic anaemia. Commercial manufacture of the drug has been discontinued by at least one major manufacturer but supplies can still be obtained on special request, particularly for patients with dermatitis herpetiformis in which condition it has been claimed to be beneficial.

General Description

Sulfamethoxypyridazine is a sulfonamide antibiotic mainly used to prevent infections as well as conditions such as coccidiosis, diarrhea and gastroenteritis.

Pharmaceutical Applications

3-Sulfanilamido-6-methoxypyridazine. Properties are similar to those of sulfadimethoxine. A rapidly absorbed, long-acting compound (half-life 38 h) with a high degree of protein binding (96%). A 1 g oral dose achieves a peak plasma concentration of around 100 mg/L after 5 h. Its use has been largely discontinued because of frequent adverse effects, but there are reports of benefit in dermatitis herpetiformis. It has been used in combination with trimethoprim.

Synthesis

Sulfamethoxypyridazine, N1 -(6-methoxy-3-pyridazinyl)sulfanilamide (33.1.43), is synthesized by replacing the chlorine atom in 6-chloro-3-(4-aminobenzenesulfonilamido)pyridazine with a methoxy group in 33.1.42 using sodium methoxide. The initial 6-chloro-3-(4-aminobenzenesulfonylamido)-pyridazine (33.1.42) is in turn synthesized by reacting 4-aminobenzenesulfanilamide with easily accessible 3,6-dichloropyridazine.

Synthesis_80-35-3

7252-84-8
121-60-8
80-35-3
Synthesis of Sulfamethoxypyridazine from 3-Amino-6-methoxypyridazine and N-Acetylsulfanilyl chloride

Sulfamethoxypyridazine Preparation Products And Raw materials

Global Suppliers ( 325)
Supplier Tel Email Country ProdList Advantage
Guilin Pharmaceutical Works -- jszl@guilinpharma.com China 33 67
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
future industrial shanghai co., ltd 400-0066400 13621662912 sales@jonln.com China 1989 65
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Capot Chemical Co., Ltd +86 (0) 571 85 58 67 18 China 18187 66
Adamas Reagent, Ltd. 400-6009262 15618770481 yhx@titansci.com China 14098 59
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50

View Latest Price from Sulfamethoxypyridazine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sulfamethoxypyridazine USP/EP/BP pictures 2026-08-20 Sulfamethoxypyridazine USP/EP/BP
80-35-3
$1.10 1g 99.9% 100 Tons Min Dideu Industries Group Limited
Sulfamethoxypyridazine pictures 2026-03-20 Sulfamethoxypyridazine
80-35-3
$10.00 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
Sulfamethoxypyridazine pictures 2025-12-25 Sulfamethoxypyridazine
80-35-3
$1.00 1kg 99% 10 Zhejiang J&C Biological Technology Co.,Limited

Sulfamethoxypyridazine Spectrum

Sulfametoxipiridazine Sulfanilamide, N1-(6-methoxy-3-pyridazinyl)- Sulfapyridazine Sulfdurazin Sulfozona Sultirene Surirene Vinces Sulfamethoxopyridazine SULFAMETHOXYPYRIDAZINE STANDARD SOLUTION SULFAMETHOXYPYRIDAZINE VETRANAL, 250 sulfamethoxypyridazine solution SULPHAMETHOXYPYRIDAZINE(SMP) sulfadimoxine, SASP N1-(6-methoxypyridazin-3-yl)sulphanilamide Sulfamethoxyp Sulfamethoxypyridazine Solution, 100ppm sulfmethoxypyridazine Sulphanyl acid N-(6-methoxypyridazin-3-yl) amide 4-Amino-N-(6-methoxy-3-pyridazinyl)benzenesulfonamide N-(6-Methoxy-3-pyridazinyl)sulfanilamide Depovernil Durox Kineks Kinex Kynex Lederkyn Lentac Lisulfen Longin Medicel Midikel Myasul Mylosul n(sup1)-(6-methoxy-3-pyridazinyl)-sulfanilamid n(sup1)-(6-methoxy-3-pyridazinyl)sulfanilamide N1-(6-Methoxy-3-pyridazinyl)sulfanilamide Opinsul Paramid Paramid supra paramidsupra Petrisul Piridolo Quinoseptyl Retamid Retasulfin RP 7522 rp7522 Slosul SMPZ Spofadazine Sulfalex N1-(6-Methoxy-3-pyridazinyl)sulfanilamide 7522RP Exazol Grosul 4-amino-N-(6-methoxypyridazin-3-yl)benzenesulfonamide 4-azanyl-N-(6-methoxypyridazin-3-yl)benzenesulfonamide N1-(6-Methoxy-d3-3-pyridazinyl)sulfanilamide, 4-Amino-N-(6-methoxy-d3-3-pyridazinyl)benzenesulfonamide