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75983-36-7

  • Product Name:4,8-dimethyldecanal
  • Molecular Formula:C12H24 O
  • Molecular Weight:184.322
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Product Details

Purity:99%

Manufacturer Sells Best Quality 4,8-dimethyldecanal 75983-36-7 with stock

  • Molecular Formula:C12H24 O
  • Molecular Weight:184.322
  • Vapor Pressure:0.0498mmHg at 25°C 
  • Boiling Point:235.5°C at 760 mmHg 
  • Flash Point:102.1°C 
  • PSA:17.07000 
  • Density:0.82g/cm3 
  • LogP:3.81800 

4,8-dimethyldecanal(Cas 75983-36-7) Usage

General Description

4,8-dimethyldecanal is a naturally occurring organic compound primarily found in citrus fruits, characterized by its strong, sweet, and citrus-like aroma. 4,8-dimethyldecanal belongs to the family of Aldehydes, specifically the Aliphatic Acyclic Aldehydes. 4,8-dimethyldecanal is used in the food and beverage industry to give a fruity and citrus flavor, while in the cosmetic industry, it's used as a fragrance ingredient. This substance is typically synthesized in a laboratory setting for industrial usage, but it is also naturally formed during the ripening process of certain citrus fruits, including oranges and mandarins. Despite its common usage, there are concerns about its potential toxicity and allergenic effects, and therefore its usage is regulated in cosmetics and food products.

InChI:InChI=1/C12H24O/c1-4-11(2)7-5-8-12(3)9-6-10-13/h10-12H,4-9H2,1-3H3

75983-36-7 Relevant articles

PHEROMONES OF INSECTS AND THEIR ANALOGS. XXVII. SYNTHESIS OF 10-HYDROXY-4,8-DIMETHYLDECA-4E,8E-DIENOIC ACID AND OF RACEMIC 4,8-DIMETHYLDECANAL FROM GERANYL ACETATE

Odinokov, V. N.,Ishmuratov, G. Yu.,Ladenkova, I. M.,Muslukhov, R. R.,Tolstikov, G. A.

, p. 234 - 237 (1991)

10-Hydroxy-4,8-dimethyldeca-4E,8E-dienoi...

Pheromone synthesis. Part 259: Synthesis of seven methyl-branched hydrocarbons as the pheromone candidates for female Korean apricot wasp, Eurytoma maslovskii

Mori, Kenji,Yang, Chang Yeol

, p. 4593 - 4607 (2016/07/07)

Seven new methyl-branched hydrocarbons w...

Deuterated analogues of 4,8-dimethyldecanal, the aggregation pheromone of Tribolium castaneum: Synthesis and pheromonal activity

Kim, Junheon,Matsuyama, Shigeru,Suzuki, Takahisa

, p. 921 - 934 (2007/10/03)

To elucidate the deuterium isotope effec...

A CONVENIENT SYNTHESIS OF RACEMIC 4,8-DIMETHYLDECANAL, THE AGGREGATION PHEROMONE OF Tribolium castaneum AND Tribolium confusum

Kovalev, B. G.,Nasser, Fadel Ahmed,Sorochinskaya, A. M.

, p. 569 - 571 (2007/10/02)

A convenient synthesis of racemic 4,8-di...

OZONOLYSIS OF ALKENES AND THE REACTIONS OF POLYFUNCTIONAL COMPOUNDS LII. SELECTIVE OZONOLYSIS OF (E)-2,7-OCTADIENAL AND (E)-3,7-DIMETHYL-2,6-OCTADIENAL IN THE SYNTHESIS OF INSECT PHEROMONES

Odinokov, V. N.,Ishmuratov, G. Yu.,Sokol'skaya, O. V.,Galeeva, R. I.,Muslukhov, R. R.,Tolstikov, G. A.

, p. 19 - 23 (2007/10/02)

The partial ozonolysis of (E)-2,7-octadi...

75983-36-7 Process route

2,6,10-trimethyldodecane-2,3-diol
114088-43-6

2,6,10-trimethyldodecane-2,3-diol

4,8-dimethyldecan-1-al
75983-36-7

4,8-dimethyldecan-1-al

Conditions
Conditions Yield
With periodic acid dihydrate; In tetrahydrofuran; at 0 - 5 ℃; for 0.333333h;
73%
4,8-Dimethyldecan-1-ol
28339-05-1

4,8-Dimethyldecan-1-ol

4,8-dimethyldecan-1-al
75983-36-7

4,8-dimethyldecan-1-al

Conditions
Conditions Yield
With pyridinium chlorochromate; In dichloromethane; for 1h; Ambient temperature;
68%
With pyridinium chlorochromate; In dichloromethane; at 20 - 22 ℃; for 3h;
67%
With pyridinium chlorochromate; In dichloromethane; for 1h; Yield given; Ambient temperature;
With pyridinium chlorochromate; In dichloromethane;

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