Mandarin aldehyde (CAS N° 20407-84-5)​

Photo credits: ScenTree SAS

Mandarin aldehyde

Aldehydes > Mandarin

Trans-2-Dodécénal ; Mandarine Aldehyde ; Trans-3-nonyl acrolein ; Valencial®

Mandarin aldehyde (CAS N° 20407-84-5)​

Photo credits: ScenTree SAS



Company Ingredient Name Learn more Naturality Certifications MOQ Purity
PCW logo MANDARINE ALDEHYDE (10%CE)
ALDM-1
Discover - 10 grs -
PCW logo TRANS 2 DODECENAL
T2DO-1
Discover - 10 grs -
Quosentis logo Aldéhyde Mandarine - 30gr Discover - 30grs -
dsm-firmenich logo MANDARIN ALDEHYDE 10 TEC
965765
Discover Molecules - -
MANE logo TRANS-2-DODECENAL
M_0062898
Discover Naturel - -
PCW logo
MANDARINE ALDEHYDE (10%CE)

ALDM-1

Discover
PCW logo
TRANS 2 DODECENAL

T2DO-1

Discover
Quosentis logo
Aldéhyde Mandarine - 30gr
Discover
dsm-firmenich logo
MANDARIN ALDEHYDE 10 TEC

965765

Discover
MANE logo
TRANS-2-DODECENAL

M_0062898

Discover
General Presentation

General Presentation

  • CAS N° :

    20407-84-5
  • EINECS number :

    243-797-2
  • FEMA number :

    2402
  • FLAVIS number :

    5,144
  • JECFA number :

    1350
  • Volatility :

    Head/Heart
  • Price Range :

    €€€
Physico-chemical properties

Physico-chemical properties

  • Appearance :

    Pale yellow liquid
  • Density :

    0,841 - 0,849 @25°C
  • Refractive Index @20°C :

    1,455 – 1,459 @20°C
  • Optical rotation :

    Donnée indisponible.
  • Vapor pressure :

    0,01 mmHg @20°C 0,0105 mmHg @25°C
  • Flash Point :

    113°C (235,4°F)
  • Molecular formula :

    C12H22O
  • Molecular Weight :

    182,31 g/mol
  • Log P :

    4,53
  • Fusion Point :

    Donnée indisponible.
  • Boiling Point :

    126°C (258,8°F)
  • Detection Threshold :

    Donnée indisponible.
Chemistry & Uses

Chemistry & Uses

Uses in perfumery :

Mandarin Aldehyde is used for all types of perfumes, for fresh notes. Used in floral-aldehydic, coniferous, ambery notes, for a contribution of a characteristic aldehydic note. Brings freshness, boosts the head and gives tenacity to citrus notes.

Year of discovery :

Data not available.

Natural availability :

Mandarin Aldehyde can be extracted from Coriander Leaf EO in its natural state, where it is present at about 20%.

Isomerism :

Mandarin Aldehyde has two diastereoisomers (Z) and (E). The isomer (E) in most often used in perfumery, to the detriment of the isomer (Z). Concentration of trans isomer is minimum 93%

Synthesis precursor :

Mandarin Aldehyde forms a Schiff base by reaction with Methyl Anthranilate or Indole for example.

Synthesis route :

Mandarin Aldehyde is an aliphatic aldehyde. As other aldehydes, it can be synthesized by reacting dodecenyl halides (chloride for example) with dimethyl sulfoxide (DMSO), followed by an alkaline treatment with sodium bicarbonate. Other synthesis routes exist using a Rosenmund reaction from dodecenic acid and an acid chloride.

Stability :

Aldehydes may form diethylacetals in alcoholic perfumes, with no real impact on their smell

Other comments :

comparing it to other aldehydesas Aldehyde C-12 lauric, Mandarin Aldehyde has a more fuity smell of Mandarin Yellow EO.

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