펜에틸 벤조에이트

펜에틸 벤조에이트
펜에틸 벤조에이트 구조식 이미지
카스 번호:
94-47-3
한글명:
펜에틸 벤조에이트
동의어(한글):
페네틸벤조산;펜에틸벤조에이트;페네틸벤조에이트;페네틸 벤조산
상품명:
FEMA 2860
동의어(영문):
FEMA 2860;202-284-3;Phenethylbenzoat;PHENETHYL BENZOATE;PHENYLETHYLBENZOAT;FEMA 2860 USP/EP/BP;PHENYLETHYL BENZOATE;2-Phenethyl benzoate;2-phenylethylbenzoate;2-Phenylethyl benzoate
CBNumber:
CB1283363
분자식:
C15H14O2
포뮬러 무게:
226.27
MOL 파일:
94-47-3.mol
MSDS 파일:
SDS

펜에틸 벤조에이트 속성

끓는 점
182 °C12 mm Hg(lit.)
밀도
1.093 g/mL at 25 °C(lit.)
증기압
0.015Pa at 25℃
굴절률
n20/D 1.56(lit.)
FEMA
2860 | PHENETHYL BENZOATE
인화점
>230 °F
물리적 상태
액체
색상
무색의
냄새
100.00%에서. 부드러운 장미 발삼 꿀 꽃무늬
?? ??
꽃향기
수용성
207.21mg/L at 25℃
LogP
3.815 at 25℃
CAS 데이터베이스
94-47-3
EPA
Benzoic acid, 2-phenylethyl ester (94-47-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
WGK 독일 2
RTECS 번호 DH6288000
HS 번호 29163100
독성 The acute oral LD50 in rats was reported to be 5 g/kg and the acute dermal LD50 in rabbits exceeded 5 g/kg (Wohl 1974).
기존화학 물질 KE-02708
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
1 0

펜에틸 벤조에이트 C화학적 특성, 용도, 생산

화학적 성질

Clear colorless liquid

출처

Reported found in the essential oil from flowers of rose and orange, in bilberry, cinnamon leaf, cassia leaf, malay apple and sea buckthorn.

용도

Phenethyl Benzoate is a building block used in the synthetic preparation of esters using Bi(OTf)3 catalyzed acylation of alcohols with acid anhydrides.

제조 방법

From phenethyl alcohol and benzoyl chloride in the presence of NaOH; from phenylethyl alcohol and methylbenzoate; by esterification of phenylethyl acohol with benzoic acid.

신진 대사

The metabolism of benzoic acid has been extensively studied in more than 20 species, including man (Williams, 1959). Depending on species and other factors, such as availability of glycine, benzoic acid may be excreted in the urine as hippuric acid, benzoyl glucuronide or other compounds (see, for example, Bridges. French. Smith & Williams, 1970; Irjala, 1972; Kato, 1972; Martin, 1966; Runyan, 1971; Strahl & Barr, 1971; Wan & Riegelman, 1972). The major route of biotransformation of benzoic acid in man is conjugation with glycine to form hippuric acid, the rate-limiting factor in this reaction being the availability of glycine (Amsel & Levy. 1969). In man at a dose of 1 mg/kg, benzoic acid is excreted entirely as hippuric acid (Bridges et al. 1970). Phenylethyl alcohol is oxidized almost entirely to phenylacetic acid (Williams, 1959). In rabbits, a small amount of benzoic acid is also formed; the phenylacetic acid is excreted mainly as phenaceturic acid (Smith, Smithies & Williams, 1954).

펜에틸 벤조에이트 준비 용품 및 원자재

원자재

준비 용품


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