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M4031

Sigma-Aldrich

p-Menthane-1,8-diol monohydrate

Synonym(s):

cis-4-Hydroxy-α,α,4-trimethylcyclohexanemethanol monohydrate, cis-Terpin monohydrate, cis-p-Menthane-1,8-diol monohydrate

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About This Item

Empirical Formula (Hill Notation):
C10H20O2 · H2O
CAS Number:
2451-01-6
Molecular Weight:
190.28
EC Number:
201-288-2
MDL number:
MFCD00149225
UNSPSC Code:
12352100
PubChem Substance ID:
57654382
NACRES:
NA.22

SMILES string

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 key

JGKJMBOJWVAMIJ-OFAZAQPOSA-N

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Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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.
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
Donald R Barnard et al.
Journal of medical entomology, 39(6), 895-899 (2002-12-24)
IR3535, KBR3023, para-Menthane-3,8-diol (PMD), and deet were evaluated in controlled studies with human subjects (n = 5) for repellency to black salt marsh mosquitoes (Ochlerotatus taeniorhynchus Wiedemann), in the Everglades National Park, FL. In tests of 6-h duration, with an
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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