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| Company | Ingredient Name | ID | Comments | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|---|
|
ROSALVA | - |
Visit website
|
- | 10 grs | - |
General Presentation
-
CAS N° :
13019-22-2 -
EINECS number :
235-878-6 -
FEMA number :
Donnée indisponible. -
FLAVIS number :
02.138
-
JECFA number :
Donnée indisponible. -
Volatility :
Head/Heart -
Price Range :
€€
Physico-chemical properties
-
Appearance :
Colorless liquid -
Density :
0,845 -
Refractive Index @20°C :
Data not available. -
Optical rotation :
Data not available. -
Vapor pressure :
0.0060 mmHg @23°C -
Flash Point :
99°C (210,2°F)
-
Molecular formula :
C10H20O -
Molecular Weight :
156,27 g/mol -
Log P :
3,7 -
Fusion Point :
Donnée indisponible. -
Boiling Point :
236°C (456,8°F) -
Detection Threshold :
1,6 ng/l air
Chemistry & Uses
Uses in perfumery :
Rosalva® is used in marine, violet flower, aldehydic, green and aromatic notes. Used more generally in floral notes.
Year of discovery :
Data not available.
Natural availability :
Rosalva® is found in Cardamom EO and in trace amounts in cognac, but it is not extracted naturally. Only the synthetic compound is used in perfumery.
Isomerism :
One of the isomers of Rosalva® is used in perfumery: 2-decenol (the alcene function is placed on carbon 2 rather than 9), which smell is more waxy and ozonic. Therefore, two positional isomers can have a very different smell. Rosalva® is a constitutional isomer of Patchone, L-Menthol, Dihydromyrcenol and Citronellol, although it has a much more rosy and honeyed smell.
Synthesis precursor :
Rosalva® is not a precursor to the synthesis of another compound of olfactory interest.
Synthesis route :
Rosalva® is an aliphatic alcohol synthesized by a partial dehydration of 1,10-decandiol.
Stability :
Stable in perfumes and diverse functional bases
Other comments :
Comparing it to Rosyrane Super®, Rosalva® has a distinctive mushroom note.
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment
