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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
Last updated:2026-01-13 11:13:26
Product description Number Pack Size Price
Sulfamethoxypyridazine European Pharmacopoeia (EP) Reference Standard S2150000 50 mg $164
Sulfamethoxypyridazine VETRANAL?, analytical standard 46858 250mg $74.8
Sulfamethoxypyridazine >98.0%(HPLC)(T) S0591 5g $30
Sulfamethoxypyridazine >98.0%(HPLC)(T) S0591 25g $81
Sulfamethoxypyridazine ≥95% 21875 5g $32
More product size

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)
pka 6.7(at 25℃)
form Crystalline Powder
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)  GHS hazard pictograms
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(23)

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 2026-03-19 Buy
Sigma-Aldrich 46858 Sulfamethoxypyridazine VETRANAL?, analytical standard 80-35-3 250mg $74.8 2026-03-19 Buy
TCI Chemical S0591 Sulfamethoxypyridazine >98.0%(HPLC)(T) 80-35-3 5g $30 2026-03-19 Buy
TCI Chemical S0591 Sulfamethoxypyridazine >98.0%(HPLC)(T) 80-35-3 25g $81 2026-03-19 Buy
Cayman Chemical 21875 Sulfamethoxypyridazine ≥95% 80-35-3 5g $32 2024-03-01 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 $32 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( 323)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Chuanghai Biotechnology Co., Ltd
+8615350571055 Sibel@chuanghaibio.com China 8738 58
Hebei Yanxi Chemical Co., Ltd.
+8618531123677 faithe@yan-xi.com China 5853 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718; +8613336195806 sales@capot.com China 29640 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21592 55
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +8618949832763 info@tnjchem.com China 2988 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29821 58
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8615060885618 sales@amoychem.com China 6369 58
Shanghai Longyu Biotechnology Co., Ltd.
+8619521488211 info@longyupharma.com China 2542 58
Hebei shuoxi biotechnology co. LTD
+8613081092107 CHINA 964 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49977 58

View Lastest Price from Sulfamethoxypyridazine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sulfamethoxypyridazine pictures 2026-03-20 Sulfamethoxypyridazine
80-35-3
US $10.00 / KG 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
Sulfamethoxypyridazine pictures 2025-12-25 Sulfamethoxypyridazine
80-35-3
US $1.00 / kg 1kg 99% 10 Zhejiang J&C Biological Technology Co.,Limited
Sulfamethoxypyridazine USP/EP/BP pictures 2025-11-18 Sulfamethoxypyridazine USP/EP/BP
80-35-3
US $1.10 / g 1g 99.9% 100 Tons Min Dideu Industries Group Limited

Sulfamethoxypyridazine Spectrum

Sulfametoxipiridazine Sulfanilamide, N1-(6-methoxy-3-pyridazinyl)- Sulfapyridazine Sulfdurazin Sulfozona Sulphamethoxypyridazine 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