CITRONELLOL

CITRONELLOL 구조식 이미지
카스 번호:
26489-01-0
상품명:
CITRONELLOL
동의어(영문):
FEMA 2307;FEMA 2309;CITRONELLOL AJ;CITRONELLOL 96;CITRONELLOL 80;DL-CITRONELLOL;DL-B-CITRONELLOL;CITRONELLOL PRIME;CITRONELLOL EXTRA;CITRONELLOL 90/92
CBNumber:
CB3377987
분자식:
C10H20O
포뮬러 무게:
156.27
MOL 파일:
26489-01-0.mol

CITRONELLOL 속성

녹는점
77-83 °C(lit.)
끓는 점
225 °C(lit.)
밀도
0.857 g/mL at 25 °C(lit.)
증기 밀도
5.4 (vs air)
증기압
~0.02 mm Hg ( 25 °C)
굴절률
n20/D 1.456(lit.)
인화점
209 °F
저장 조건
2-8°C
CAS 데이터베이스
26489-01-0(CAS DataBase Reference)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 26-36
WGK 독일 1
RTECS 번호 RH3400000
그림문자(GHS): GHS 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
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.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P321 (…) 처치를 하시오.
P332+P313 피부 자극이 생기면 의학적인 조치· 조언을 구하시오.
P333+P313 피부자극성 또는 홍반이 나타나면 의학적인 조치·조언를 구하시오.
P362 오염된 의복을 벗고 세척 후에 재사용하기
P363 다시 사용전 오염된 의류는 세척하시오.
P501 ...에 내용물 / 용기를 폐기 하시오.

CITRONELLOL C화학적 특성, 용도, 생산

화학적 성질

The enantiomers (3R)-(+)-citronellol and (3S)-(?)-citronellol occur in many essential oils.
(?)-Citronellol isolated from natural sources is often named rhodinol. At present, the name rhodinol is also used for the isopropenyl isomer α-citronellol or a mixture of the two isomers.
In many natural products, citronellol occurs as a mixture of its two enantiomers; the pure (+) or (?) formis seldom found. (?)-Citronellol is the predominant enantiomer in geranium and rose oils, both of whichmay contain up to 50% citronellols. Citronellol is a colorless liquid with a sweet rose-like odor. The odor of (?)- citronellol is more delicate than that of (+)-citronellol.
Citronellol undergoes the typical reactions of primary alcohols. Compared with geraniol, which contains one more double bond, citronellol is relatively stable. Citronellol is converted into citronellal by dehydrogenation or oxidation; hydrogenation yields 3,7-dimethyloctan-l-ol. Citronellyl esters are easily prepared by esterification with acid anhydrides.

제조 방법

(?)-Citronellol is still obtained mainly from geranium oil by saponification followed by fractional distillation (“rhodinol”). Although of high odor quality, this grade does not possess the true (?)-citronellol odor due to impurities. Much larger quantities of (+)-citronellol and racemic citronellol are used and are prepared by partial or total synthesis.
1) Synthesis from citronellal: Citronellal can be hydrogenated to citronellol by the use of special catalysts and/or special hydrogenation techniques, for example, [122]. The citronellal that is used as the starting material may originate from synthetic production or from isolation of essential oils. Citronellal from citronella oil yields (+)-citronellol; the corresponding material from citronellal from Eucalyptus citriodora oil is racemic. Pure (+)-citronellol is also obtained from (+)-citronellal, which is produced as an intermediate of (?)-menthol. By this asymmetric technology, pure (?)-citronellal and, therefore, pure (?)-citronellol are also available.
2) Synthesis of racemic or slightly dextrorotatory citronellol from geraniol fractions of essential oils: This citronellol is produced by catalytic hydrogenation of saponified geraniol fractions (also containing (+)- citronellol) obtained from Java citronella oil, followed by fractional distillation. Selective hydrogenation of the double bond in the 2-position of geraniol in geraniol–citronellol mixtures isolated from essential oils can be achieved by using Raney cobalt as a catalyst; overhydrogenation to 3,7-dimethyloctan-l-ol can be largely avoided by this method.
3) Synthesis of racemic citronellol from synthetic geraniol, nerol, or citral: A considerable amount of commercial synthetic racemic citronellol is produced by partial hydrogenation of synthetic geraniol and/or nerol. Another starting material is citral, which can be hydrogenated, for example, in the presence of a catalyst system consisting of transition metals and amines.
4) Preparation of (?)-citronellol from optically active pinenes: (+)-cis-Pinane is readily synthesized by hydrogenation of (+)-α-pinene or (+)-β-pinene and is then pyrolyzed to give (+)-3,7-dimethyl-1,6-octadiene. This compound can be converted into (?)-citronellol (97% purity) by reaction with triisobutylaluminumor diisobutylaluminumhydride, followed by air oxidation and hydrolysis of the resulting aluminum alcoholate.

색상 색인 번호

L-Citronellol is a constituent of rose and geranium oils. d-Citronellol occurs in Ceylon and Java citronella oils. As a fragrance allergen, citronellol has to be mentioned by name in cosmetics within the EU.

CITRONELLOL 준비 용품 및 원자재

원자재

준비 용품


CITRONELLOL 공급 업체

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