68-35-9
- Product Name：Sulfadiazine
- Molecular Formula：C10H10N4O2S
- Purity：99%
- Molecular Weight：250.281
Product Details;
CasNo： 68-35-9
Molecular Formula： C10H10N4O2S
Appearance： White to slightly yellow crystalline powder
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What is the Sulfadiazine ?
Sulfadiazine is White to slightly yellow crystalline powder, while it's Molecular Formula is C10H10N4O2S. DMSO soluble potent immunosuppressant, neuroprotective neuroregenerative, in vitro T cell proliferation blocker. disrupts calcineurin-mediated signal transduction in T lymphocytes
What is the CAS number for Sulfadiazine ?
The CAS number of Sulfadiazine is 68-35-9.
More information of Sulfadiazine 68-35-9 are:
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Synonyms |
Sulfanilamide,N1-2(1H)-pyrimidinylidene- (6CI);Sulfanilamide, N1-2-pyrimidinyl- (8CI);2-(4-Aminobenzenesulfonylamino)pyrimidine;2-(p-Aminobenzenesulfonamido)pyrimidin;4-Amino-N-(2-pyrimidinyl)benzenesulfonamide;4-[[(Pyrimidin-2-yl)amino]sulfonyl]aniline;Adiazine;Cremodiazine;Debenal;Deltazina;Di-Azo-Mul;Diazin;Diazovit;Diazyl;Lipo-Levazine;Liquadiazine;N1-2-Pyrimidylsulfanilamide;Neazine;Pirimal;Pyrimal;RP 2616;Spofadrizine;Sterazine;Sulfadiazine;Sulfapirimidin;Sulfazin (Russian pharmaceutical);Sulfazine;Sulfolex;Sulphadiazine E;Sulfadiazine (SD); |
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CAS Number |
68-35-9 |
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Molecular Formula |
C10H10N4O2S |
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Molecular Weight |
250.281 |
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Density |
1.496 g/cm3 |
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Melting Point |
254 °C |
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Boiling Point |
512.6 °C at 760 mmHg |
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Flash Point |
263.8 °C |
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HS CODE |
29335990 |
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PSA |
106.35000 |
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LogP |
2.59460 |
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Pka |
pKa 2.21(H2O t = 25 I = 0.5 (NaCl)) (Uncertain) |
What is Sulfadiazine (68-35-9) used for?
Sulfadiazine is an oral sulfonamide anti-bacterial agent. it is a synthetic pyrimidinyl sulfonamide derivative, The chemical classification of sulfadiazine is Sulfonamides.The sulfonamides are synthetic bacteriostatic antibiotics with a wide spectrum against most gram-positive and many gram-negative organisms. However, many strains of an individual species may be resistant. Sulfonamides inhibit multiplication of bacteria by acting as competitive inhibitors of p-aminobenzoic acid in the folic acid metabolism cycle. Bacterial sensitivity is the same for the various sulfonamides, and resistance to one sulfonamide indicates resistance to all. Most sulfonamides are readily absorbed orally. However, parenteral administration is difficult, since the soluble sulfonamide salts are highly alkaline and irritating to the tissues. The sulfonamides are widely distributed throughout all tissues. High levels are achieved in pleural, peritoneal, synovial, and ocular fluids. Although these drugs are no longer used to treat meningitis, CSF levels are high in meningeal infections. Their antibacterial action is inhibited by pus. Sulfadiazine is used in combination with pyrimethamine to treat toxoplasmosis in patients with acquired immunodeficiency syndrome and in newborns with congenital infections.
InChI:InChI=1/C10H10N4O2S/c11-8-2-4-9(5-3-8)17(15,16)14-10-12-6-1-7-13-10/h1-7H,11H2,(H-,12,13,14,15,16)
Articles related to Sulfadiazine:
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Article |
Source |
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Synthesis method of sulfadiazine |
- Paragraph 0017-0032, (2021/03/13) |
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Synthesis of calix[4]azacrown substituted sulphonamides with antioxidant, acetylcholinesterase, butyrylcholinesterase, tyrosinase and carbonic anhydrase inhibitory action |
Akocak, Suleyman,Boga, Mehmet,Kalay, Erbay,Lolak, Nebih,Nocentini, Alessio,Oguz, Mehmet,Supuran, Claudiu T.,Yilmaz, Mustafa , p. 1215 - 1223 (2020/05/27) |
How to get the best price on Sulfadiazine?
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