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Cetyl Alcohol → Menthol

HRID 34261
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인쇄 미리보기

반응식

HRID 34261 반응식
C(O)(=[O:19])CCCCCCC/C=C\C/C=C\CCCCC.C(OC(C)C)(=[O:35])CCCCCCCCCCCCC.C(O)CCCCCCCCCCCCCCC.[CH3:57][C:58]1([CH3:67])[O:63][C:62]2([CH3:66])[CH2:64][CH2:65][CH:59]1[CH2:60][CH2:61]2>>[CH:62]1([CH3:66])[CH2:64][CH2:65][CH:59]([CH:58]([CH3:67])[CH3:57])[CH:60]([OH:19])[CH2:61]1.[CH3:57][C:58]1([CH3:67])[O:63][C:62]2([CH3:66])[CH2:64][CH2:65][CH:59]1[CH2:60][CH2:61]2.[C:62]12([CH3:66])[C:58]([CH3:67])([CH3:57])[CH:59]([CH2:65][CH2:64]1)[CH2:60][C:61]2=[O:35]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 2682Cetyl AlcoholHCID 27581,8-CineoleHCID 8042Isopropyl MyristateHCID 5280450Linoleic Acid

생성물 3

HCID 1254MentholHCID 2537CamphorHCID 27581,8-Cineole

실험 절차

Linoleic acid (5 parts) and isopropyl myristate (2 parts) are added to cetyl alcohol (70 parts) molten at 50° C. A solution obtained by successively dissolving menthol (0.25 part), eucalyptol (0.5 part) and camphor (0.25 part) in cineol (3 parts), at a temperature of the order of 20° C., is added to the resulting solution. This gives a phase φ1.

후처리

  1. custommolten at 50° C

출처 및 근거

ORD 기록
ord-7d966831b1e5421f9d8b486f7d7cf4f3
출처 데이터셋
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04761407

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