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1 See also  





2 References  














Rhodinol






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From Wikipedia, the free encyclopedia
 


Rhodinol
Rhodinol molecule
Names
Preferred IUPAC name

(3S)-3,7-Dimethyloct-7-en-1-ol

Other names

α-Citronellol, 3,7-Dimethyl-(6- or 7-)octen-1-ol, 3,7-Dimethyl-7-octen-1-ol, 1-Citronellol

Identifiers

CAS Number

3D model (JSmol)

ChEMBL
ChemSpider
ECHA InfoCard 100.004.977 Edit this at Wikidata
EC Number
  • 229-887-4
  • 205-473-9
  • PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • C[C@H](CCO)CCCC(C)=C

    Properties

    Chemical formula

    C10H20O
    Molar mass 156.269 g·mol−1
    Hazards
    GHS labelling:

    Pictograms

    GHS02: FlammableGHS07: Exclamation markGHS09: Environmental hazard

    Signal word

    Danger

    Hazard statements

    H315, H317, H318, H319, H411

    Precautionary statements

    P261, P264, P272, P273, P280, P302+P352, P305+P351+P338, P310, P321, P332+P313, P333+P313, P337+P313, P362, P363, P391, P501

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Rhodinol is the chemical compound 3,7-dimethyloct-7-en-1-ol. As the (3S) isomer it is CAS 6812-78-8, and as the racemate it is CAS 141-25-3.

    In the field of perfumery materials, the term may refer to L-citronellol, to mixtures comprising mostly L- or racemic citronellol and geraniol, or to mixtures comprising mostly racemic 3,7-dimethyloct-7-en-1-ol and racemic citronellol.

    Two example synthetic Rhodinol products are Rhodinol 70, a racemic mixture comprising 40–60% 3,7-dimethyloct-7-en-1-ol and 40–60% citronellol, and Sigma-Aldrich Rhodinol, which consists of L-citronellol and geraniol.

    Rhodinol is also provided in perfumery in natural grades as materials extracted from geraniumorcitronella, comprising principally citronellol and geraniol.

    Rhodinol products are used in cosmetics and perfumery to impart flowery odors, particularly but not limited to being a component of rosy odor.[1]

    3,7-Dimethyloct-7-en-1-ol does not appear substantively in nature.[2]

    See also

    [edit]

    References

    [edit]
    1. ^ Rhodinol The Good Scents Company
  • ^ The Citronellol Problem and the Isolation of α-Citronellol Journal of the American Chemical Society
  • t
  • e
  • t
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  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Rhodinol&oldid=1224730450"

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