CITRONELLOL
|
|
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
- n
20/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)
그림문자(GHS): | |||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
신호 어: | Warning | ||||||||||||||||||||||||
유해·위험 문구: |
|
||||||||||||||||||||||||
예방조치문구: |
|
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
글로벌( 41)공급 업체
공급자 | 전화 | 이메일 | 국가 | 제품 수 | 이점 |
---|---|---|---|---|---|
Hubei Jusheng Technology Co.,Ltd. | 18871490254 |
linda@hubeijusheng.com | CHINA | 28172 | 58 |
Career Henan Chemica Co | +86-0371-86658258 +8613203830695 |
laboratory@coreychem.com | China | 30239 | 58 |
Mainchem Co., Ltd. | +86-0592-6210733 |
sale@mainchem.com | China | 32343 | 55 |
3B Pharmachem (Wuhan) International Co.,Ltd. | 821-50328103-801 18930552037 |
3bsc@sina.com | China | 15839 | 69 |
Zhengzhou Acme Chemical Co., Ltd. | 0371-037163312495,13303845143 13303845143 |
3001379618@qq.com | China | 10386 | 58 |
Hebei Zhenjia new material Co., LTD | 0319-5925599 13315915972 |
13313090628@163.com | China | 2916 | 58 |
CITRONELLOL 관련 검색:
게라니올 로디놀 초산 시트로넬릴 시트로넬롤
RHODINOL
SPECIAL RHODINOL
RHODINOL EX GERANIUM
Rhodinol, (S)-3,7-Dimethyl-6-octen-1-ol,B-Rhodinol,β-Rhodinol, (S)-(-)-β-Citronellol, (S)-3,7-Dimethyl-6-octen-1-ol,BETA-RHODINOL,L-RHODINOL
Cyclomethylene rhodinol
RHODINOL G,RHODINOL 70,RHODINOL
RHODINOL EX GERANIUM OIL
Natural rhodinol, butylated