Detail of > 22199-08-2
- MSDS Download

- CAS Number:
- 22199-08-2
- Name:
Silver,[4-amino-N-(2-pyrimidinyl-kN1)benzenesulfonamidato-kO]-
- Superlist Name:
- Silver sulfadiazine
- Formula:
- C10H9AgN4O2S
- Molecular Structure:
![Molecular Structure of 22199-08-2 (Silver,[4-amino-N-(2-pyrimidinyl-kN1)benzenesulfonamidato-kO]-)](http://www.lookchem.com/300w/2010/0620/22199-08-2.jpg)
- Synonyms:
- Silver,(4-amino-N-2-pyrimidinylbenzenesulfonamidato-NN,O1)-;Sulfanilamide,N1-2-pyrimidinyl-, monosilver(1+) salt (8CI);Benzenesulfonamide,4-amino-N-2-pyrimidinyl-, silver complex;Dermazin;Flamazine;Flammazine;Geben;NSC 625324;Silvadene;Silver 2-sulfanilamidopyrimidine;Silverol;Sulfadiazine silver;
- Molecular Weight:
- 357.13
- EINECS:
- 244-834-5
- Melting Point:
- 285 °C (dec.)(lit.)
- Boiling Point:
- 512.6 °C at 760 mmHg
- Flash Point:
- 263.8 °C
- Appearance:
- solid
- Hazard Symbols:
Xi- Risk Codes:
- 36/37/38
- Safety:
- 26-36Details
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Reference
- Administration of silver sulfadiazine and radioactive derivatives
- Administration of silver sulfadiazine and radioactive derivatives. Wysor, Michael S. (Kalil, Eugene J., USA). U.S. US 4020150 26 Apr 1977, 5 pp. (English). (United States of America). CODEN: USXXAM. CLASS: IC: A61K043-00. NCL: 424001000. APPLICATION: US 73-415637 14 Nov 1973. DOCUMENT TYPE: Patent CA Section: 1 (Pharmacodynamics) Section cross-reference(s): 8 An aq. suspension of silver sulfadiazine (I) [22199-08-2] administered orally or s.c. in doses of 1,050 mg/kg, once daily for 5 days cured mice of Plasmodium berghei infection (malaria) even after splenectomy. Parositemia was eliminated in 1 to 3 days. The antimalarial activity of I was not inhibited by p-aminobenzoic acid indicating a mode of action different from that of the sulfonamides. Doses of 1,050 mg I/kg/day orally or s.c. were also effective against systemic Pseudomonas aeruginosa infections in mice. I and silver sulfamethoxydiazine localized in the PC-6 tumor system in the same manner as sulfadiazine. 111Ag-labeled I is therefore proposed as a neoplasm inhibitor, the localization of radiation within the tumor serving to eradicate malignant cells. No acute or chronic toxicity was obsd. in mice on administration of 1,050 mg I/kg/day for 30 days, however, i.p. administration was toxic in doses ranging from 550-1,050 mg I/kg.
- Silver sulfadiazine (AgSD) resistant Pseudomonas infection in experimental burn wounds
- Silver sulfadiazine (AgSD) resistant Pseudomonas infection in experimental burn wounds. Modak, S. M.; Stanford, J. W.; Bradshaw, W.; Fox, C. L., Jr. (Coll. Physicians Surg., Columbia Univ., New York, NY, USA). Panminerva Med., 25(3), 181-8 (English) 1983. CODEN: PMMDAE. ISSN: 0031-0808. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) Section cross-reference(s): 10 The in vitro and in vivo efficacy of silver sulfadiazine (I) [22199-08-2] and other metal sulfadizaines and bactericides against several I-resistant strains of Pseudomonas aeurigonasa is reported. Apparently, there are 2 types of bacterial strains; those sensitive to I in vitro and in vivo; and, those sensitive to I in vitro but resistant to the drug in vivo. 55-56-1 and 7440-48-4 are just another two chemicals used in this study. A comparative study of the growth and pathogenic properties of these 2 different Pseudomonas strains is presented. .
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