Perfluorobutyl iodide

Perfluorobutyl iodide 구조식 이미지
카스 번호:
423-39-2
상품명:
Perfluorobutyl iodide
동의어(영문):
NONAFLUOROBUTYL IODIDE;NONAFLUORO-1-IODOBUTANE;1,1,1,2,2,3,3,4,4-NONAFLUORO-4-IODOBUTANE;C1014NH3;uorobutyL;Perfluoroiodobutane;PERFLUOROBUTYL IODODE;PERFLUOROBUTYL IODIDE;1-Iodoperfluorobutane;1-IODONONAFLUOROBUTANE
CBNumber:
CB9474482
분자식:
C4F9I
포뮬러 무게:
345.93
MOL 파일:
423-39-2.mol
MSDS 파일:
SDS

Perfluorobutyl iodide 속성

녹는점
-88 °C
끓는 점
66-67 °C
밀도
2.01 g/mL at 25 °C(lit.)
굴절률
n20/D 1.3285(lit.)
인화점
None
저장 조건
Keep in dark place,Inert atmosphere,Room temperature
물리적 상태
액체
Specific Gravity
2.010
색상
클리어 퍼플
수용성
섞일 수 없음
감도
Light Sensitive
BRN
1777546
노출 한도
ACGIH: TWA 0.01 ppm
안정성
안정적인. 알칼리성 용액과 호환되지 않습니다.
InChIKey
PGRFXXCKHGIFSV-UHFFFAOYSA-N
CAS 데이터베이스
423-39-2(CAS DataBase Reference)
NIST
1-Iodononafluorobutane(423-39-2)
EPA
Butane, 1,1,1,2,2,3,3,4,4-nonafluoro-4-iodo- (423-39-2)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 26-36-37/39
유엔번호(UN No.) 2810
WGK 독일 3
RTECS 번호 EK5360000
F 고인화성물질 8
위험 참고 사항 Irritant/Light Sensitive
TSCA T
위험 등급 6.1(b)
포장분류 III
HS 번호 29034700
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H411 장기적 영향에 의해 수생생물에 유독함 수생 환경유해성 물질 - 만성 구분 2
예방조치문구:
P273 환경으로 배출하지 마시오.
P391 누출물을 모으시오.
P501 ...에 내용물 / 용기를 폐기 하시오.
NFPA 704
1
2 1

Perfluorobutyl iodide MSDS


1,1,1,2,2,3,3,4,4-Nonafluoro-4-iodobutane

Perfluorobutyl iodide C화학적 특성, 용도, 생산

개요

Perfluorobutyl iodide (PFBI) is a promising alternative to chlorofluorocarbon solvents used in aircraft ground maintenance operations and other military and commercial operations because it cleans well, has zero ozone depletion potential, and has extremely low global warming properties. Perfluorobutyl iodides also could used as gain media for a solar-pumped laser amplifier. This compound is usually utilized as perfluoroalkyl radical precursors[1–3].

화학적 성질

clear colourless liquid with pungent odour

용도

Perfluorobutyl Iodide is used as an organocatalyst in some polymerization reactions.

Synthesis

Add 10 mol of triphenylphosphine chloride and 50 mol of N-methylimidazole hydrochloride to methanol and stir to dissolve. Heat to 50°C, add 65 moles of aluminum chloride, stir and dissolve, continue the reaction for 2 hours, raise the temperature to 80°C, evaporate the solvent, and filter to remove the insoluble matter to obtain quaternary ammonium salt and N-alkyl imidazole salt composite aluminum acid. Salt ionic liquid. Add 2 kg of the aluminate ionic liquid prepared in step S1 to the reaction kettle equipped with a reflux device, then add 264 g of perfluoropentanoic acid and raise the temperature to 80°C. Slowly add 2.5 mol of iodine ethanol solution dropwise within 5 hours. After the dropwise addition is completed, heat to 100°C for 8 hours. The reaction solution was allowed to stand and separated into layers to separate the aluminate ionic liquid and product layers. The product layer was purified by distillation to obtain 336g of Perfluorobutyl iodide.

Perfluorobutyl iodide 준비 용품 및 원자재

원자재

준비 용품


Perfluorobutyl iodide 공급 업체

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