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Home > Encyclopedia > Sulfamethoxypyridazine

Sulfamethoxypyridazine

pharmaceutical raw materials
Sulfamethoxypyridazine structure

Sulfamethoxypyridazine 

structure
  • CAS No:

    80-35-3

  • Formula:

    C11H12N4O3S

  • Chemical Name:

    Sulfamethoxypyridazine

  • Synonyms:

    Benzenesulfonamide,4-amino-N-(6-methoxy-3-pyridazinyl)-;Sulfanilamide,N1-(6-methoxy-3-pyridazinyl)-;4-Amino-N-(6-methoxy-3-pyridazinyl)benzenesulfonamide;CL 13,494;3-(p-Aminobenzenesulfamido)-6-methoxypyridazine;Davosin;Depovernil;Kinex;Kynex;Medicel;Lederkyn;N1-(6-Methoxy-3-pyridazinyl)sulfanilamide;6-Methoxy-3-sulfanilamidopyridazine;Midicel;Midikel;Myasul;Paramid;Paramid Supra;Spofadazine;Sulfalex;3-Sulfanilamido-6-methoxypyridazine;Sultirene;6-Sulfanilamido-3-methoxypyridazine;Sulfamethoxypyridazine;Sulfapyridazine;Retamid;Retasulfine;3-(4-Aminobenzenesulfonamido)-6-methoxypyridazine;Retasulphine;Retasulfin;Quinoseptyl;Sulfapiridazin;Davozil;Lederkin;3-Methoxy-6-sulfanilamidopyridazine;SMOP;Sulfozona;Altezol;Piridolo;Lisulfen;Longin;Slosul;Sulphamethoxypyridazine;6-Methoxy-3-pyridazinylsulfanilamide;LAS (pharmaceutical);LAS;Sulfdurazin;CL 13494;RP 7522;88538-49-2

  • Categories:

    Organic Chemistry  >  Amides

Description

Sulfamethoxypyridazine is a long-acting sulfonamide antibiotic, for treatment of Dermatitis herpetiformis.


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.|Sulfamethoxypyridazine is a long-acting sulfonamide antibiotic.|A sulfanilamide antibacterial agent.

Sulfamethoxypyridazine Basic Attributes

280.3

280.30

201-272-5

T034E4NS2Z

757875

DTXSID5023611

C80795

J - Antiinfectives for systemic use

2935009090

Characteristics

116

0.3

White to yellow Crystalline Powder

1.48318 g/cm3

182.5 °C

564.9°C at 760 mmHg

295.4±32.9 °C

1.647

579.5mg/L(25 ºC)

2-8°C

Oral-rat LD50: 2739 mg/kg; Oral-Mouse LD50: 1750 mg/kg

Flammable; burning produces toxic nitrogen oxides and sulfur oxide fumes

159.4 Ų [M+H]+ [CCS Type: TW, Method: calibrated with polyalanine and drug standards]

Safety Information

NONH for all modes of transport

2

37/38-41

26-39

WP0400000

Xi

Warehouse ventilated, low temperature and dry

P280-P305 + P351 + P338 + P310

H315-H318-H335

|Danger|H315 (45.83%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P272, P280, P285, P302+P352, P304+P340, P304+P341, P305+P351+P338, P310, P312, P321, P332+P313, P333+P313, P342+P311, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 101 companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Toxicity

moderately toxic

Drug Information

Substances that inhibit the growth or reproduction of BACTERIA. (See all compounds classified as Anti-Bacterial Agents.)

Sulfamethoxypyridazine

Sulfamethoxypyridazine Use and Manufacturing

Uses

Antibacterial.

Pharmaceuticals -> Animal Drugs -> Approved in Taiwan

Computed Properties

Molecular Weight:280.31
XLogP3:0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:280.06301143
Monoisotopic Mass:280.06301143
Topological Polar Surface Area:116
Heavy Atom Count:19
Complexity:376
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Extract from the above information

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

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