Photo credits: ScenTree SAS

Woody > Sandalwood > Milky > Grapefruit > Leather

Sandalore®

3-methyl-5-(2,2,3-trimethyl-1-cyclopent-3-enyl)pentan-2-ol ; Dersantol ; Landasweet ; Pentamethyl cyclopent-3-ene butanol ; Alpha,beta,2,2,3-pentamethyl cyclopent-3-ene-1-butanol ; Sandal pentanol ; Sandal touch ; Sandalorex ; Sandasweet

Photo credits: ScenTree SAS

Company	Ingredient Name	ID	Comments	Naturality	Certifications	MOQ	Purity
	Sandalore - 30 Gr	-	Visit website	-		-	-

Sandalore - 30 Gr

Certifications :

General Presentation

CAS N° :
65113-99-7
EINECS number :
265-453-0
FEMA number :
Donnée indisponible.
FLAVIS number :
Donnée indisponible.

JECFA number :
Donnée indisponible.
Volatility :
Base
Price Range :
€€

Physico chemical properties

Appearance :
Colorless viscous liquid
Density :
0,898
Refractive Index @20°C :
Data not available.
Optical rotation :
Data not available.
Vapor pressure :
Data not available.
Flash Point :
95°C

Molecular formula :
C₁₄H₂₆O
Molecular Weight :
210,36 g/mol
Log P :
4,7
Fusion Point :
<-50°C
Boiling Point :
275°C
Detection Threshold :
Donnée indisponible.

Chemistry & Uses

Uses in perfumery :

Sandalore® is used in sandalwood reproductions, woody notes for bringing volume and trail. Used for a milky and creamy effect in sandalwood notes. To be combined with other sandalwood notes such as Sandela®, Bacdanol® or Polysantol®. Not to be put in candle base. Tends to flatten accords.

Year of discovery :

1976

Natural availability :

Sandalore® is not available in its natural state.

Isomerism :

The isomer of Sandalore® formed during the synthesis has a ramified alcohol function, while Sandalore® has it on its main carbon chain. Sandalore® has two asymmetric carbons. It is therefore a mixture of isomers that is used even when Sandalore® is isolated. Adoxal® is a constitutional isomer of Sandalore®. Its smell is however radically different, as it is marine and aldehydic.

Synthesis precursor :

Sandalore® is not a precursor to the synthesis of another compound of olfactory interest.

Synthesis route :

Sandalore® is synthesized by a condensation of Campholenal with Methyl Ethyl Ketone. Then, two compounds are obtained and catalytically hydrogenated to ensure a selectivity of this hydrogenation (the alcene function of the ring must not be hydrogenated). A mixture of two hydrogenated molecules is obtained. These two isomers can be separated by a fractional distillation, or used together, as their smell is similar. The term Sandalore® refers to only one of these two molecules.

Stability :

Unstable in acid cleaners and in very alkaline products.

Other comments :

Sandalore® is less milky than Sandela® and less potent than Bacdanol®.

Regulations & IFRA

Allergens :

This ingredient does not contain any allergen.

IFRA 51^th :

This ingredient is restricted by the 51th amendment

Restriction type :

RESTRICTION

Cause of restriction :

DERMAL SENSITIZATION

Amendment :

Quantitative limit on the use :

Cat.1	Cat.2	Cat.3	Cat.4	Cat.5 A B C D		Cat.6
0,21 %	0,062 %	1,2 %	1,2 %	0,29 % 0,29 % 0,29 % 0,29 %		0,68 %
Cat.5 A B C D			Cat.6
0,29 % 0,29 % 0,29 % 0,29 %			0,68 %
Cat.7 A B		Cat.8	Cat.9	Cat.10 A B	Cat.11 A B	Cat.12
2,4 % 2,4 %		0,12 %	2,3 %	8,1 % 8,1 %	4,5 % 4,5 %	No Restriction
Cat.10 A B	Cat.11 A B	Cat.12
8,1 % 8,1 %	4,5 % 4,5 %	No Restriction

Sandalore®

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General Presentation

CAS N° :

EINECS number :

FEMA number :

FLAVIS number :

JECFA number :

Volatility :

Price Range :

Physico chemical properties

Appearance :

Density :

Refractive Index @20°C :

Optical rotation :

Vapor pressure :

Flash Point :

Molecular formula :

Molecular Weight :

Log P :

Fusion Point :

Boiling Point :

Detection Threshold :