Tetrahydrolinalool (CAS N° 78-69-3)​

Photo credits: ScenTree SAS

Tetrahydrolinalool

Floral > Fresh Flowers > Zesty

3,7-Dimethyloctan-3-ol

Tetrahydrolinalool (CAS N° 78-69-3)​

Photo credits: ScenTree SAS

Company Ingredient Name ID Comments Naturality Certifications MOQ Purity
BASF logo
Tetrahydrolinalool 30786547 Visit website Je me procure cet ingrédient Molecule - -
BASF logo
Tetrahydrolinalool BMBcert™ 30786547 Visit website Je me procure cet ingrédient Molecule - -
PCW logo
TETRAHYDROLINALOOL TETL-1 Visit website Je me procure cet ingrédient - 10 grs 99.0 - 100.0

Tetrahydrolinalool

ID : 30786547

Certifications :

Tetrahydrolinalool BMBcert™

ID : 30786547

Certifications :

TETRAHYDROLINALOOL

ID : TETL-1

Chine

Certifications :

Information Générales

General Presentation

  • CAS N° :

    78-69-3
  • EINECS number :

    201-133-9
  • FEMA number :

    3060
  • FLAVIS number :

    Donnée indisponible.
  • JECFA number :

    357
  • Volatility :

    Head
  • Price Range :

    Data not available.
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Colorless liquid
  • Density :

    0,826
  • Refractive Index @20°C :

    Donnée indisponible.
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,75 mmHg @20°C 2,25 mmHg @50°C
  • Flash Point :

    77°C (170,6°F)
  • Molecular formula :

    C10H22O
  • Molecular Weight :

    158,28 g/mol
  • Log P :

    3,3
  • Fusion Point :

    197°C (386,6°F)
  • Boiling Point :

    197°C (386,6°F)
  • Detection Threshold :

    0,02 μg/l
Utilisation

Chemistry & Uses

Uses in perfumery :

Tetrahydrolinalool is a product used mainly to replace linalool in applications where the latter may not be stable enough. It serves as a more stable alternative to linalool, although it has a fresher and more technical scent.

Year of discovery :

Data not available.

Natural availability :

Tetrahydrlinalool is present in nature.

Isomerism :

Data not available.

Synthesis precursor :

Tetrahydrolinalool is not used to prepare other products used in perfumery

Synthesis route :

May be prepared by hydrogenation of linalool

Stability :

Tetrahydrolinalool is very stable is all kind of commun application, it is more stable than the linalol itself.

Other comments :

Data not available.

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