술파디아진

술파디아진
술파디아진 구조식 이미지
카스 번호:
68-35-9
한글명:
술파디아진
동의어(한글):
설파다이아진;술파디아진;설파디아진
상품명:
Sulfadiazine
동의어(영문):
SULPHADIAZINE;Sulfadiazine,(S);SULFADIAZIN;Sulfose;Terfonyl;Diazolone;Neotrizine;Sulfadiazene;SULPHADIAZINE BP;-AMino-N-2-pyriMidinylbenzenesulfonaMide
CBNumber:
CB4166214
분자식:
C10H10N4O2S
포뮬러 무게:
250.28
MOL 파일:
68-35-9.mol
MSDS 파일:
SDS

술파디아진 속성

녹는점
253 °C (dec.) (lit.)
끓는 점
512.6±52.0 °C(Predicted)
밀도
1.3780 (rough estimate)
굴절률
1.6440 (estimate)
저장 조건
2-8°C
용해도
디메틸설폭사이드에 용해됩니다.
산도 계수 (pKa)
pKa 2.21(H2O t = 25 I = 0.5 (NaCl)) (Uncertain)
물리적 상태
가루
색상
하얀색
수용성
67.13mg/L(25℃)
Merck
14,8903
BRN
6733588
BCS Class
4/3
CAS 데이터베이스
68-35-9(CAS DataBase Reference)
NIST
Sulfadiazine(68-35-9)
EPA
Benzenesulfonamide, 4-amino-N-2-pyrimidinyl- (68-35-9)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,Xi
위험 카페고리 넘버 22-36/37/38-42/43-43-42
안전지침서 26-36
유엔번호(UN No.) 3249
WGK 독일 3
RTECS 번호 WP1925000
F 고인화성물질 10
TSCA Yes
위험 등급 6.1(b)
포장분류 III
HS 번호 29335990
독성 LD50 oral in mouse: 1500mg/kg
기존화학 물질 KE-01586
그림문자(GHS): GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
H362 모유를 먹는 아이에게 유해할 수 있음 생식독성 물질,수유 또는 수유기에 미치는 영향 추가 카테고리 P201, P260, P263, P264, P270,P308+P313
H411 장기적 영향에 의해 수생생물에 유독함 수생 환경유해성 물질 - 만성 구분 2
예방조치문구:
P202 모든 안전 조치 문구를 읽고 이해하기 전에는 취급하지 마시오.
P260 분진·흄·가스·미스트·증기·...·스프레이를 흡입하지 마시오.
P263 임신·수유 기간에는 접촉하지 마시오.
P273 환경으로 배출하지 마시오.
P301+P312 삼켜서 불편함을 느끼면 의료기관(의사)의 진찰을 받으시오.
P308+P313 노출 또는 접촉이 우려되면 의학적인 조치· 조언를 구하시오.
NFPA 704
1
2 0

술파디아진 C화학적 특성, 용도, 생산

화학적 성질

White to slightly yellow crystalline pow

용도

It is used in the form of silver salts (sulfadiazine silver) as an external antibacterial agent, primarily for treating burns. It is believed that the presence of the silver ion in the molecule facilitates increased antimicrobial and wound-healing action.

정의

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

Antimicrobial activity

Sulfadiazine is somewhat more active than other sulphonamides.

일반 설명

Sulfadiazine’s plasma half-life is 17 hours. It is a white,odorless crystalline powder soluble in water to the extentof 1:8,100 at 37°C and 1:13,000 at 25°C, in human serumto the extent of 1:620 at 37°C, and sparingly soluble in alcoholand acetone. It is readily soluble in dilute mineralacids and bases. Its pKa is 6.3.

Pharmaceutical Applications

Sulfadiazine is almost insoluble in water and unstable on exposure to light. It is administered orally or, as the sodium salt, by intravenous injection. It is a component of several multi-ingredient preparations. Its low solubility in urine led to its general replacement by other compounds. The intravenous solution is highly alkaline and should not be given by any other route.

Pharmacokinetics

Oral absorption: Very good
Cmax 3 g oral: c. 50 mg/L after 3–4 h
Plasma half-life :7–12 h
Volume of distribution: 0.36 L/kg
Plasma protein binding: c. 40%
Absorption and distribution
Adequate blood concentrations are easily achieved and maintained after oral administration. It is well distributed and penetrates in therapeutic concentrations into the CSF, but because of resistance it is no longer the drug of choice in meningitis. It crosses the placenta and enters breast milk to achieve concentrations around 20% of plasma levels.
Metabolism and excretion
Sulfadiazine is subject to acetylation in the liver. The acetyl derivative lacks antibacterial activity and is excreted more slowly (half-life 8–18 h). Parent compound and metabolite are both excreted mainly by glomerular filtration.

Clinical Use

Urinary tract infection
Nocardiasis
Chancroid
Toxoplasmosis (in combination with pyrimethamine)
Meningococcal infections
Prophylaxis of rheumatic fever

부작용

In addition to side effects common to the group, sulfadiazine inhibits the metabolism of phenytoin. The risk of crystalluria can be reduced by high fluid intake and alkalization of the urine.

Safety Profile

Poison by intravenous route. Moderately toxic by ingestion and intraperitoneal routes. Human systemic effects by ingestion: hematuria, anuria, general anesthesia, gastrointestinal effects. Experimental teratogenic and reproductive effects. When heated to decomposition it emits very toxic fumes of NOx and SOx.

술파디아진 준비 용품 및 원자재

원자재

준비 용품


술파디아진 공급 업체

글로벌( 519)공급 업체
공급자 전화 이메일 국가 제품 수 이점
Hebei Mojin Biotechnology Co., Ltd
+86 13288715578 +8613288715578
sales@hbmojin.com China 12460 58
shandong perfect biotechnology co.ltd
+86-53169958659; +8618596095638
sales@sdperfect.com China 294 58
Wuhan Quanjinci New Material Co.,Ltd.
+8615271838296
kyra@quanjinci.com China 1534 58
Shaanxi TNJONE Pharmaceutical Co., Ltd
+8618740459177
sarah@tnjone.com China 1142 58
Ouhuang Engineering Materials (Hubei) Co., Ltd
+86-86177
admin@hbouhuang.com China 2952 58
Apeloa production Co.,Limited
+8619933239880
admin@apcl.com.cn China 853 58
Henan Suikang Pharmaceutical Co.,Ltd.
+86-18239973690 +86-18239973690
sales@suikangpharm.com China 355 58
Hebei Zhuanglai Chemical Trading Co.,Ltd
+8613343047651
admin@zlchemi.com China 3002 58
Hebei Shengyang Water Conservancy Engineering Co., Ltd.
+8615373025980
clara@hbshengyang.com China 864 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21673 55

술파디아진 관련 검색:

Copyright 2019 © ChemicalBook. All rights reserved