포란

포란
포란 구조식 이미지
카스 번호:
26675-46-7
한글명:
포란
동의어(한글):
포란;포란(FORANE);이소플루란
상품명:
Isoflurane
동의어(영문):
Forane;Isoflurane266;2-Chloro-2-(difluoromethoxy)-1,1,1-trifluoroethane;1-CHLORO-2,2,2-TRIFLUOROETHYL DIFLUOROMETHYL ETHER;(2R)-2-chloro-2-(difluoroMethoxy)-1,1,1-trifluoroethane;IsofL;Forene;Aerrane;Terrell;Isourane
CBNumber:
CB8437691
분자식:
C3H2ClF5O
포뮬러 무게:
184.49
MOL 파일:
26675-46-7.mol
MSDS 파일:
SDS

포란 속성

녹는점
48.5°C
끓는 점
48.5 °C
밀도
1.510 g/mL at 25 °C
증기압
238 mmHg ( 20 °C)
굴절률
1.3002
인화점
48-49°C
저장 조건
2-8°C
용해도
물에 거의 녹지 않으며, 에탄올 및 트리클로로에틸렌과 섞입니다.
Specific Gravity
approximate 1.50
색상
무색 내지 거의 무색
수용성
클로로포름과 에틸 아세테이트에 용해됩니다. 물에 섞이거나 혼합하기 어렵지 않습니다.
Merck
14,5175
BRN
1852087
안정성
안정적인.
InChIKey
PIWKPBJCKXDKJR-UHFFFAOYSA-N
CAS 데이터베이스
26675-46-7(CAS DataBase Reference)
NIST
1-Chloro-2,2,2-trifluoroethyl difluoromethyl ether(26675-46-7)
EPA
Isoflurane (26675-46-7)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 F,T,Xn
위험 카페고리 넘버 36/37/38-67-48/20
안전지침서 26-36/37/39-24/25
유엔번호(UN No.) UN 3334
WGK 독일 3
RTECS 번호 KN6799000
위험 참고 사항 Flammable/Toxic
HS 번호 2909191800
유해 물질 데이터 26675-46-7(Hazardous Substances Data)
독성 An isomer of enflurane with similar anesthetic properties. Isoflurane has less effect on myocardial function, leaving the cardiovascular system normally responsive to epinephrine or hypercarbia, and it does not cause a marked increase in seizure susceptibility. It was not widely used because of reports that it caused increases in liver neoplasms in mice, but this observation has been challenged and the compound reintroduced.
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H336 졸음 또는 현기증을 일으킬 수 있음 특정표적장기 독성 물질(1회 노출);마취작용 구분 3 경고 P261, P271, P304+P340, P312,P403+P233, P405, P501
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P271 옥외 또는 환기가 잘 되는 곳에서만 취급하시오.
P403+P233 용기는 환기가 잘 되는 곳에 단단히 밀폐하여 저장하시오.
P405 밀봉하여 저장하시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
1
2 0

포란 C화학적 특성, 용도, 생산

화학적 성질

colourless liquid

용도

Isoflurane is a halogenated ether used for inhalational anesthesia. Recent studies suggest that there might be a relationship between administration of isoflurane and postoperative cognitive dysfunct ion (POCD).

Biological Functions

Isoflurane (Forane) is a structural isomer of enflurane and produces similar pharmacological properties: some analgesia, some neuromuscular blockade, and depressed respiration. In contrast, however, isoflurane is considered a particularly safe anesthetic in patients with ischemic heart disease, since cardiac output is maintained, the coronary arteries are dilated, and the myocardium does not appear to be sensitized to the effects of catecholamines. Also, blood pressure falls as a result of vasodilation, which preserves tissue blood flow. Isoflurane causes transient and mild tachycardia by direct sympathetic stimulation; this is particularly important in the management of patients with myocardial ischemia.
Unlike enflurane, isoflurane does not produce a seizurelike EEG pattern. Furthermore, the metabolic transformation of isoflurane is only one-tenth that of enflurane, so fluoride production is quite low. Among the halogenated hydrocarbons, isoflurane is one of the most popular, since it preserves cardiovascular stability and causes a low incidence of untoward effects.

일반 설명

Isoflurane is a volatile liquid (bp=48.5°C) with an MAC of1.15, a blood:gas partition coefficient of 1.43 and high solubilityin fat. Isoflurane is a structural isomer of enflurane. Itis a known respiratory irritant, but less so than desflurane.Approximately 0.2% of the administered drug undergoesmetabolism, the rest is exhaled unchanged. The metabolismof isoflurane yields low levels of the nephrotoxic fluoride ionas well as a potentially hepatotoxic trifluoroacetylating compound). The relatively low concentrations ofthese compounds have resulted in very low risks of hepatotoxicityand nephrotoxicity. There have been no reports ofseizures caused by isoflurane and only transient increases inheart rate have been reported.

Clinical Use

Isoflurane was introduced in the United States in 1981 and is a potent anesthetic agent with many similarities to its isomer enflurane (potent, nonflammable, and intermediate blood solubility). It does produce significantly fewer cardiovascular effects than enflurane, however, and it can be used safely with epinephrine without as great a concern for arrhythmia production. Isoflurane has a more pungent odor than halothane and, thus, can cause irritation to the throat and respiratory tract, triggering coughing and laryngospasm. To overcome this problem, it often is supplemented with intravenous agents. Less than 0.2% of an administered dose is metabolized, mostly to fluoride and trifluoroacetic acid. Some minimal potential for hepatotoxicity is associated with a trifluoroacetyl halide metabolite.

포란 준비 용품 및 원자재

원자재

준비 용품


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