Dihydromyrcenol

한글명:Dihydromyrcenol

카스 번호53219-21-9

상품명:Dihydromyrcenol

CBNumberCB2161684

분자식C10H20O

포뮬러 무게156.27

MOL 파일53219-21-9.mol

화학적 성질

끓는 점	91 °C(Press: 10 Torr)
색상	무색의 약간 점성이 있는 오일
CAS 데이터베이스	53219-21-9
EPA	7-Octen-2-ol, 2-methyl-6-methylene-, dihydro deriv. (53219-21-9)

위험 및 안전 성명

위험품 표기

위험 카페고리 넘버

안전지침서

독성

The acute oral LD₅₀ in rats was reported as 3.6 g/kg (3.0-4.2 g/kg) (Mor eno, 1973). The acute dermal LD₅₀ value in rabbits exceeded 5 g/kg (Moreno, 1973).

NFPA 704:

	2
1		0

그림문자(GHS)

Dihydromyrcenol MSDS

Dihydromyrcenol 화학적 특성, 용도, 생산

개요
Dihydromyrcenol is a colorless liquid with a fresh citrus-like odor and a lavender note. It is obtained from 3,7-dimethyl-1,6- octadiene (citronellene), the pyrolysis product of cis-pinane and can be prepared by three different processes: (i) by addition of hydrogen chloride and subsequent hydrolysis of the resulting 2,6-dimethyl-2-chloro-7-octene; or (ii) by addition of formic acid and subsequent saponification of the resulting dihydromycrenyl formate; or (iii) by direct hydroxylation with 60–80% sulfuric acid.Dihydromyrcenol is used in fine fragrances as well as in soap and detergent perfumes for fresh lime and citrus-like floral notes.
화학적 성질
Clear Colorless liquid, insoluble in water, soluble in 4-6 volumes of 55% ethanol or 1-2 volumes of 70% ethanol, also soluble in oily fragrances. The aroma is sweet and powerful, with fresh and spicy citrus, pine and cypress, lavender, fruity, floral, sweet and sour aromas, and has white lemon and cologne flavors.
출처
Has apparently not been reported to occur in nature.
용도
Dihydromyrcenol is an organic compound from the group of the acyclic terpenoidal alcohols. It is a fragrance with a powerful, fresh, lavender like, sweet citrus and floral fragrance, which is synthetically prepared. The pure substance appears as a colorless viscous liquid, which is practically insoluble in water.
제조 방법
Dihydromyrcenol is prepared by addition of dihydromyrcene (generated from the cleavage of pinane, the hydrogenation product of pinene), with water and formic acid under acid catalysis.
By controlled, partial hydrogenation of myrcenol (Arctander, 1969).

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