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Sulfapyridine

Product Name
Sulfapyridine
CAS No.
144-83-2
Chemical Name
Sulfapyridine
Synonyms
Sulphapyridine;Sulfapyridin;Ronin;A-499;THAP11;m+b693;Trianon;Adiplon;Dagenan;Eubasin
CBNumber
CB8423160
Molecular Formula
C11H11N3O2S
Formula Weight
249.29
MOL File
144-83-2.mol
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Sulfapyridine Property

Melting point:
191-193°C
Boiling point:
473.5±51.0 °C(Predicted)
Density 
1.3220 (rough estimate)
refractive index 
1.6740 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
pKa 8.48(H2O t = 25 I = 0.05) (Uncertain)
color 
White to Off-White
Water Solubility 
<0.1 g/100 mL at 22 ºC
Merck 
14,8938
BRN 
222065
Stability:
Stable. Combustible. Protect from light. Incompatible with strong oxidizing agents.
CAS DataBase Reference
144-83-2(CAS DataBase Reference)
NIST Chemistry Reference
Sulfapyridine(144-83-2)
EPA Substance Registry System
Sulfapyridine (144-83-2)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-36-26
WGK Germany 
2
RTECS 
DA9625000
HazardClass 
IRRITANT
HS Code 
29350010
Toxicity
LD50 orally in mice: 7.5 mg/g (Wien)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Precautionary statements

P201Obtain special instructions before use.

P202Do not handle until all safety precautions have been read and understood.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P308+P313IF exposed or concerned: Get medical advice/attention.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
BP1039
Product name
Sulfapyridine
Purity
British Pharmacopoeia (BP) Reference Standard
Packaging
25MG
Price
$247
Updated
2024/03/01
Sigma-Aldrich
Product number
1634000
Product name
Sulfapyridine
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200mg
Price
$261.6
Updated
2024/03/01
TCI Chemical
Product number
S0071
Product name
Sulfapyridine
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$51
Updated
2024/03/01
Cayman Chemical
Product number
28619
Product name
Sulfapyridine
Packaging
10g
Price
$48
Updated
2024/03/01
Cayman Chemical
Product number
28619
Product name
Sulfapyridine
Packaging
25g
Price
$70
Updated
2024/03/01
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Sulfapyridine Chemical Properties,Usage,Production

Description

Sulfapyridine is a sulfonamide antibiotic with antibacterial and anti-inflammatory activities. It is also a metabolite of sulfasalazine formed through bacterial conversion in the colon. It is active against strains of Y. enterocolitica and Salmonella (MICs = 3.1-25 and 25-100 μg/ml, respectively), as well as S. aureus (MBC = 0.8 μM). It is an inhibitor of recombinant P. carinii dihydropteroate synthetase (DHPS; IC50 = 0.18 μM). Sulfapyridine scavenges peroxyl radicals in an oxygen radical absorbance capacity (ORAC) assay. It inhibits histamine release induced by compound 48/80 from isolated rat peritoneal mast cells in a dose-dependent manner. Sulfapyridine (1 μg/kg) also inhibits compound 48/80-induced systemic allergic reaction in rats. Formulations containing sulfapyridine have previously been used in the treatment of dermatological conditions and ulcerative colitis.

Chemical Properties

White to Off-White Solid

Uses

Used in treatment of dermatitis herpetiformis; antibacterial.

Uses

antibacterial, dermatitis herpetiformis therapy

Definition

ChEBI: A sulfonamide consisting of pyridine with a 4-aminobenzenesulfonamido group at the 2-position.

Antimicrobial activity

Like all sulfanilamides, this drug possesses antibacterial activity with respect to streptococci, pneumococci, staphylococci, meningococci, gonococci, colon bacillus, pathogenic dysentery, and so on. It is a long-lasting drug. Synonyms of this drug are bacillopirin, plurazol, sulfidin, and thiaseptol.

General Description

Sulfapyridine’s plasma half-life is 9 hours.This compound is a white, crystalline, odorless, and tastelesssubstance. It is stable in air but slowly darkens on exposureto light. It is soluble in water (1:3,500), in alcohol(1:440), and in acetone (1:65) at 25°C. It is freely soluble indilute mineral acids and aqueous solutions of sodium andpotassium hydroxide. The pKa is 8.4. Its outstanding effectin curing pneumonia was first recognized by Whitby; however,because of its relatively high toxicity, it has been supplantedlargely by sulfadiazine and sulfamerazine. Severalcases of kidney damage have resulted from acetylsulfapyridinecrystals deposited in the kidneys. It also causes severenausea in most patients. Because of its toxicity, it is usedonly for dermatitis herpetiformis.
Sulfapyridine was the first drug to have an outstandingcurative action on pneumonia. It gave impetus to the studyof the whole class of N1 heterocyclically substituted derivativesof sulfanilamide.

General Description

Odorless or almost odorless white or yellowish-white crystalline powder. Very slightly bitter taste. Aqueous solution is neutral.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Sulfapyridine is an amino acid. Slowly darkens on exposure to light . Soluble in both acidic and basic aqueous solutions

Fire Hazard

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

Safety Profile

Moderately toxic by intraperitoneal and intravenous routes. Slightly toxic by ingestion. Experimental reproductive effects. Human mutation data reported. Questionable carcinogen with experimental tumorigenic data. When heated to decomposition it emits very toxic fumes of NO, and SOx.

Synthesis

Sulfapyridine, N1 -(2-pyridyl)-sulfanilamide (33.1.21), is also synthesized by an analogous scheme from 4-acetylaminobenzenesulfonyl chloride and 2-amino pyridine.

Purification Methods

Crystallise sulfapyridine from 90% acetone and dry it at 90o. Its solubility in Me2CO, EtOH and H2O is 1.5%, 0.22% and 0.02%, respectively. [Winterbottom J Am Chem Soc 62 160 1940, Beilstein 22 III/IV 3978.]

Sulfapyridine Preparation Products And Raw materials

Raw materials

Preparation Products

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Sulfapyridine Suppliers

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
TAIYUAN RHF CO.,LTD.
Tel
+86 351 7031519
Fax
+86 351 7031519
Email
sales@RHFChem.com
Country
China
ProdList
2338
Advantage
56
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44689
Advantage
61
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Fax
86-027-87531808
Email
sales@chemwish.com
Country
China
ProdList
35896
Advantage
56
Pure Chemistry Scientific Inc.
Tel
001-857-928-2050 or 1-888-588-9418
Fax
001-617-206-9595
Email
sales@chemreagents.com
Country
United States
ProdList
10186
Advantage
62
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14103
Advantage
59
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32321
Advantage
50
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
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View Lastest Price from Sulfapyridine manufacturers

Hebei Weibang Biotechnology Co., Ltd
Product
Sulfapyridine 144-83-2
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-10-25
Shaanxi TNJONE Pharmaceutical Co., Ltd
Product
Sulfapyridine 144-83-2
Price
US $0.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
1000kg
Release date
2024-04-02
Hebei Mojin Biotechnology Co., Ltd
Product
Sulfapyridine 144-83-2
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-08-30

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