Photo credits: ScenTree SAS

Fruity > Green Fruits > Tropical Fruits > Juicy Fruits

Manzanate®

Applinate ; Ethyl 2-methyl pentanoate ; Ethyl 2-methyl valerate ; Ethyl 2-methyl-4-pentanoate ; Mazanate ; Melon valerate

Photo credits: ScenTree SAS

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

Manzanate - 30 Gr

Certifications :

General Presentation

CAS N° :
39255-32-8
EINECS number :
254-384-1
FEMA number :
3488
FLAVIS number :
09.526

JECFA number :
214
Volatility :
Head
Price Range :
€€

Physico chemical properties

Appearance :
Colorless liquid
Density :
0,86
Refractive Index @20°C :
Data not available.
Optical rotation :
Data not available.
Vapor pressure :
Data not available.
Flash Point :
41°C

Molecular formula :
C₈H₁₆O₂
Molecular Weight :
144,21 g/mol
Log P :
2,65
Fusion Point :
Donnée indisponible.
Boiling Point :
153°C
Detection Threshold :
0,003 ppb (0,0000000000003 %)

Chemistry & Uses

Uses in perfumery :

Manzanate® is a key molecule in masculine perfumes. It is often used in small quantities to bring a strong fruity and addictive impact from the top note of the perfume, with a metallic and green note. Also used in apple, pineapple, exotic fruits and yellow fruits notes, to bring a heady and green effect.

Year of discovery :

1974

Natural availability :

Manzanate® is not reported as found in nature.

Isomerism :

Manzanate® has one asymmetric carbon in its strcture. (R)-2-methylpentanoate and (S)-2-methylpentanoate both exist. Manzanate® is a mixture of these two enantiomers. They are not used separately. On the other hand, Ethyl Caproate is a positional isomer of Manzanate®. Its smell is less elegant and closer to ripe pineapple, less green.

Synthesis precursor :

Manzanate® is not a precursor for the synthesis of another compound used in perfumes.

Synthesis route :

Manzanate® can be synthesized by an esterification reaction between 2-methylpentanoic acid and ethanol. This reaction can be catalyzed by the presence of a strong acid in a low quantity as concentrated sulfuric acid, to enhance the reaction yield. The use of chloro-2-methylpentanoic acid can also be a help.

Stability :

Only stable in Fabric conditioner, APC and shampoo bases. Particularly unstable in liquid fabric detergent and liquid bleach

Other comments :

Manzanate® is one of the commercial keys of modern perfumery. At the right dosage, it makes the perfume more addictive, wheither it is a functional or fine fragrance. Among these keys, Verdox®, Styrallyle acetate® and Ambroxan® can also be quoted.

Manzanate®

I buy this ingredient

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 :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51^th :

Manzanate®

I buy this ingredient

I buy this ingredient

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 :

Chemistry & Uses

Uses in perfumery :

Year of discovery :

Natural availability :

Isomerism :

Synthesis precursor :

Synthesis route :

Stability :

Other comments :

Regulations & IFRA

Allergens :

IFRA 51th :

IFRA 51^th :