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Merck

M4031

Sigma-Aldrich

对薄荷烷-1,8-二醇 一水合物

别名:

反式-4-(1-羟基-1-甲基乙基)-1-甲基环己-1-醇

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About This Item

经验公式(希尔记法):
C10H20O2 · H2O
CAS号:
分子量:
190.28
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

SMILES 字串

O.CC(C)(O)[C@@H]1CC[C@](C)(O)CC1

InChI

1S/C10H20O2.H2O/c1-9(2,11)8-4-6-10(3,12)7-5-8;/h8,11-12H,4-7H2,1-3H3;1H2/t8-,10+;

InChI 密鑰

JGKJMBOJWVAMIJ-OFAZAQPOSA-N

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儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Makiko Fujii et al.
Drug development and industrial pharmacy, 30(6), 673-677 (2004-08-03)
The enhancing effect of p-Menthane-3,8-diol (MDO) on skin permeation of antipyrine (ANP) and indomethacin (IM) through Yucatan micropig skin in vitro was compared with 1-menthol. p-Menthane-3,8-diol is a metabolite of 1-menthol and has little odor. It is easy to combine
Scott P Carroll et al.
Journal of the American Mosquito Control Association, 22(3), 507-514 (2006-10-28)
para-Menthane-3,8-diol(PMD) is a monoterpene spent product of the distillation of leaves of the Australian lemon-scented gum tree (updated nomenclature Corymbia citriodora ssp. citriodora). In April 2005, the U.S. Centers for Disease Control and Prevention (CDC) endorsed two non-deet mosquito repellents
Jeremy Drapeau et al.
Chemistry & biodiversity, 6(6), 934-947 (2009-06-25)
The aim of this work is to develop a new generation of repellent products with a long-lasting protection based on a natural component, para-menthane-3,8-diol (PMD). The active is first rendered soluble in a surfactantless microemulsion (H(2)O/(i)PrOH/PMD) and then in classical
S P Bhatia et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 46 Suppl 11, S171-S175 (2008-07-22)
A toxicologic and dermatologic review of geranodyle when used as a fragrance ingredient is presented.
Stephen S Barasa et al.
Journal of medical entomology, 39(5), 736-741 (2002-09-28)
Four stereoisomers of p-menthane-3,8-diol, which make up the natural product obtained from Eucalyptus citriodora, were synthesized through stereoselective procedures. Repellency assays showed that all the four were equally active against Anopheles gambiae s.s. Racemic blends and the diastereoisomeric mixture of

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