p-페닐페놀

p-페닐페놀
p-페닐페놀 구조식 이미지
카스 번호:
92-69-3
한글명:
p-페닐페놀
동의어(한글):
키세놀;4-페닐페놀;p-페닐페놀;하이드록시비페닐
상품명:
4-Phenylphenol
동의어(영문):
BIPHENYL-4-OL;P-HYDROXYBIPHENYL;[1,1'-Biphenyl]-4-ol;P-PHENYLPHENOL;4-pp;4-HYDROXYBIPHENYL;4-HYDROXYDIPHENYL;p-Xenol;PARAXENOL;2-DIPHENYLOL
CBNumber:
CB8197379
분자식:
C12H10O
포뮬러 무게:
170.21
MOL 파일:
92-69-3.mol
MSDS 파일:
SDS

p-페닐페놀 속성

녹는점
164-166 °C (lit.)
끓는 점
321 °C (lit.)
밀도
1.0149 (rough estimate)
증기압
0Pa at 25℃
굴절률
1.6188 (estimate)
인화점
330 °F
저장 조건
Sealed in dry,Room Temperature
용해도
메탄올: 용해성50mg/mL, 투명, 무색
물리적 상태
플레이크
산도 계수 (pKa)
9.55(at 25℃)
색상
흰색에서 약간 노란색
수소이온지수(pH)
7 (0.7g/l, H2O, 20℃)
수용성
0.7g/L(20℃)
Merck
14,7305
BRN
1907452
안정성
안정적인. 강산화제, 강염기, 할로겐과 호환되지 않습니다. 타기 쉬운.
LogP
3.6 at 25℃
CAS 데이터베이스
92-69-3(CAS DataBase Reference)
NIST
p-Hydroxybiphenyl(92-69-3)
EPA
4-Phenylphenol (92-69-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi,N
위험 카페고리 넘버 36/37/38-51/53-38
안전지침서 26-36/37-61-36
유엔번호(UN No.) UN3077
WGK 독일 2
RTECS 번호 DV5850000
TSCA Yes
위험 등급 9
포장분류 III
HS 번호 29071900
유해 물질 데이터 92-69-3(Hazardous Substances Data)
독성 LD50 ipr-mus: 150 mg/kg NTIS** AD691-490
기존화학 물질 KE-02871
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H317 알레르기성 피부 반응을 일으킬 수 있음 피부 과민성 물질 구분 1 경고 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H411 장기적 영향에 의해 수생생물에 유독함 수생 환경유해성 물질 - 만성 구분 2
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P272 작업장 밖으로 오염된 의복을 반출하지 마시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
NFPA 704
0
2 0

p-페닐페놀 MSDS


4-Hydroxybiphenyl

p-페닐페놀 C화학적 특성, 용도, 생산

화학적 성질

light tan solid (odour threshold detection limit 0.7 ppm)

용도

Fluorescence and phosphorescence quantum yields and fluorescence and phosphorescence lifetimes were obtained for 4-phenylphenol adsorbed on filter paper with either NaCl, NaBr, or NaI at 296 and 93 K. The solid-surface fluorescence and phosphorescence quantum yield values and phosphorescence lifetime values were obtained for p-aminobenzoic acid (PABA) and 4-phenylphenol adsorbed on α-cyclodextrin/NaCl mixtures. 4-Phenylphenol is used as an antioxidant and is a potential EDC.

제조 방법

4-phenylphenol synthesis: Add to a 50 ml round-bottom flask, in this order, 122 mg of phenylboronic acid, 414 mg of potassium carbonate, 220 mg of 4-iodophenol, and 10 ml of deionized water. Weigh in a suitably sized container 3 mg Pd on C 10%, add 1 ml of deionized water, and stir gently by hand to form a slurry that is then transferred to the reaction flask.
synthesis of 4-phenylphenol
Couple the flask to a water-jacketed condenser, and reflux the mixture on a hot plate with a magnetic stirrer vigorously for 30 min (until a precipitate appears). After this time, switch off the plate and allow to cool to r.t. Add HCl 2 M to an acidic pH (check with indicator paper). Separate the resulting solid, still containing the catalyst, by filtering with a Hirsch funnel. Wash the solid with 10 ml of water. Then, in a Hirsch funnel, add 10 ml of MeOH, and collect the filtrate in a clean container. Add to the resulting MeOH solution 10 ml of deionized water to obtain the precipitate of the product. Purify by recrystallization, heating in a water bath container with the precipitate and the MeOH/H2O mixture. If necessary, add 1 to 2 ml more of hot MeOH, to finish dissolving the solid. Filter under vacuum with a Hirsch funnel, air dry the solid (can recover the next day). Weigh and calculate the yield.

정의

ChEBI: 4-Phenylphenol is a member of the class of hydroxybiphenyls that is biphenyl carrying a hydroxy group at position 4.

일반 설명

4-Phenylphenol undergoes enzymatic polymerization and polymer developed is characterized by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. It is the intermediate in manufacture of 4-alkyl substituted phenol-formaldehyde resins.

Safety Profile

Acute poison by intraperitonealroute. Questionable carcinogen with experimentalcarcinogenic and tumorigenic data. When heated todecomposition it emits acrid, irritating fumes.

Purification Methods

Crystallise the phenol from aqueous EtOH, *C6H6, and dry it in a vacuum over CaCl2 [Buchanan et al. J Am Chem Soc 108 7703 1986]. [Beilstein 6 IV 4600.]

p-페닐페놀 준비 용품 및 원자재

원자재

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