암브록스DL

암브록스DL
암브록스DL 구조식 이미지
카스 번호:
3738-00-9
한글명:
암브록스DL
동의어(한글):
암브록스DL
상품명:
AMBROX DL
동의어(영문):
Cetalox;Ambermor;AMBERLYN;AMBROX DL;Ambraoxide;AMBERLYN 50;Iridium ether;CETALOX 922560;amber naphthofuran;AMBROX DL, FIRMENICH
CBNumber:
CB9272233
분자식:
C16H28O
포뮬러 무게:
236.39
MOL 파일:
3738-00-9.mol

암브록스DL 속성

녹는점
75-76 °C
끓는 점
273.9±8.0 °C(Predicted)
밀도
0.939±0.06 g/cm3(Predicted)
FEMA
3471 | 1,5,5,9-TETRAMETHYL-13-OXATRICYCLO(8.3.0.0(4,9))TRIDECANE
냄새
디프로필렌 글리콜 중 10.00%. 드라이 우디 앰버 앰버그리스 머스크 스위트
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호박색
JECFA Number
1240
LogP
5.41
EPA
Naphtho[2,1-b]furan, dodecahydro-3a,6,6,9a-tetramethyl- (3738-00-9)

안전

기존화학 물질 KE-12820

암브록스DL C화학적 특성, 용도, 생산

화학적 성질

3a,6,6,9a-Tetramethyldodecahydronaphtho[2,1-b]furan is a crystalline autoxidation product of ambrein with a typical ambergris odor. It is prepared from (?)-sclareol, a diterpene alcohol obtained from extraction of clary sage plants. Oxidative degradation to a lactone (“sclareolide”), hydrogenation of the latter to the corresponding diol, and dehydration yield the title compound.

출처

Reported found in clary sage oil.

제조 방법

Racemic sclareolide can be prepared by cyclization of homofarnesic acid in the presence of SnCl4 as a catalyst . Pure diastereomers are obtained by acid cyclization of (E)- and (Z)-4-methyl-6-(2,6,6-trimethylcyclohex-l(2)-enyl)-3- hexen-1-ol, prepared from 2-methyl-4-(2,6,6-trimethylcyclohex-l(2)-enyl)-2- butenal [394]. If the racemic sclareolide mixture is resolved into its enantiomers, the (–)-oxide may also be obtained by a totally synthetic route

상품명

Compound starting from natural sclareol: Ambermore, Ambermore-DL, Ambermore-EX (Aromor), Ambrox® Super (Firmenich), Ambroxan® (Kao), Ambroxide (Symrise); compound starting from homofarnesic acid derivatives: Ambrox® DL (Firmenich); compound starting from 2-methyl- 4-(2,6,6-trimethylcyclohex-l(2)enyl)-2-butenal: Cetalox® (Firmenich), Cetalor (Aromor).

암브록스DL 준비 용품 및 원자재

원자재

준비 용품


암브록스DL 공급 업체

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