에틸트라이메틸벤조일페닐포스피네이트

에틸트라이메틸벤조일페닐포스피네이트
에틸트라이메틸벤조일페닐포스피네이트 구조식 이미지
카스 번호:
84434-11-7
한글명:
에틸트라이메틸벤조일페닐포스피네이트
동의어(한글):
에틸트라이메틸벤조일페닐포스피네이트
상품명:
Ethyl (2,4,6-trimethylbenzoyl) phenylphosphinate
동의어(영문):
TPO-L;BENZOPHENONE-1;Photoinitiator TPO-L;ethyl trimethylbenzoyl phenylphosphinate;ethyl phenyl(2,4,6-trimethylbenzoyl)phosphinate;IHT-PI TPO-L;4-BENZORESORCINOL;2,4,6-Trimethylbenzoyldi-Phenylphosphinate;2,4,6-TRIMETHYLBENZOYLPHENYLPHOSPHINIC ACID ETHYL ESTER;SYNSORB
CBNumber:
CB9855469
분자식:
C18H21O3P
포뮬러 무게:
316.33
MOL 파일:
84434-11-7.mol
MSDS 파일:
SDS

에틸트라이메틸벤조일페닐포스피네이트 속성

녹는점
144.5-147 °C(lit.)
끓는 점
456.0±55.0 °C(Predicted)
밀도
1.14
증기압
0Pa at 20℃
저장 조건
under inert gas (nitrogen or Argon) at 2-8°C
용해도
71.8g/L in organic solvents at 20 ℃
물리적 상태
Oil to Thick Oil
색상
무색~황색
수용성
35mg/L at 25℃
InChI
InChI=1S/C18H21O3P/c1-5-21-22(20,16-9-7-6-8-10-16)18(19)17-14(3)11-13(2)12-15(17)4/h6-12H,5H2,1-4H3
InChIKey
ZMDDERVSCYEKPQ-UHFFFAOYSA-N
SMILES
P(C1=CC=CC=C1)(C(=O)C1=C(C)C=C(C)C=C1C)(OCC)=O
LogP
2.91 at 25℃
CAS 데이터베이스
84434-11-7(CAS DataBase Reference)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36
안전지침서 26
WGK 독일 2
RTECS 번호 DJ0700000
기존화학 물질 2004-3-2701
그림문자(GHS): GHS 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
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.

에틸트라이메틸벤조일페닐포스피네이트 C화학적 특성, 용도, 생산

Synthesis

0.1 mol phenylphosphinic acid and 100 mL chlorobenzene were added to the reaction vessel. 0.11 mol 2,4,6-trimethylbenzaldehyde was added dropwise under controlled temperature, followed by 2 hours of incubation at 100-120°C. After cooling, pH was adjusted to 4-6 with hydrochloric acid, then 0.13 g vanadium acetylacetonate was added as a catalyst. 0.15 mol of 35% hydrogen peroxide was added dropwise at a rate of 5-10 drops per minute, with the mixture insulated at 5-10°C. The reaction was monitored by TLC until completion.
The reaction mixture was diluted with 100 mL water, neutralized with saturated sodium bicarbonate, and the organic layer was separated and washed twice with water. Excess oxidant was reduced with aqueous sodium sulfite, and the organic layer was separated and washed again. The mixture was dehydrated with anhydrous sodium sulfate, filtered to remove the desiccant.
To the dehydrated organic layer, 0.11 mol sodium hydroxide was added, followed by dropwise addition of 0.55 mol diethyl sulfate at 60-80°C. After the reaction was complete, the mixture was adjusted to pH 8-10 with sodium hydroxide, washed with water, and the organic layer was separated. The organic layer was dried over anhydrous sodium sulfate, filtered, and the solvent was evaporated under reduced pressure to yield Ethyl phenyl(2,4,6-trimethylbenzoyl)phosphinate.

에틸트라이메틸벤조일페닐포스피네이트 준비 용품 및 원자재

원자재

준비 용품


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