18485-38-6

Basic information

• Product Name: 2 4-DODECADIEN-1-OL
• Synonyms: (e,e)-4-dodecadien-1-ol;(2E,4E)-dodeca-2,4-dienol;Dodecadien-1-ol;2,4-Dodecadien-1-ol, (2E,4E)-;2,4-DODECADIENE-1-OL (MIXTURE OF STEREOISOMERS);(2E,4E)-2,4-Dodecadien-1-ol;(E,E)-2,4-Dodecadien-1-ol;2,4-Dodecadien-1-ol, (E,E)-
• CAS NO: 18485-38-6
• Molecular Formula: C₁₂H₂₂O
• Molecular Weight: 182.30248
• EINECS: 242-372-9
• Product Categories: Biochemistry;Higher Fatty Acids & Higher Alcohols;Unsaturated Higher Alcohols
• Mol File: 18485-38-6.mol

Chemical Properties

• Melting Point: 27 °C
• Boiling Point: 274.9°Cat760mmHg
• Flash Point: 109 °C
• Appearance: /
• Density: 0.862g/cm³
• Vapor Pressure: 0.000664mmHg at 25°C
• Refractive Index: 1.473
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2 4-DODECADIEN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 2 4-DODECADIEN-1-OL(18485-38-6)
• EPA Substance Registry System: 2 4-DODECADIEN-1-OL(18485-38-6)

Safety Data

• Hazardous Substances Data: 18485-38-6(Hazardous Substances Data)

Usage

Uses

Used in Fragrance and Flavor Industry:
2,4-Dodecadien-1-ol is used as a key component in the synthesis of various scents and flavors, contributing to the creation of unique and appealing aromas and tastes in a wide range of products.
Used in Pheromone Research and Applications:
In the field of entomology, 2,4-Dodecadien-1-ol is utilized for its natural occurrence in insect pheromones, particularly in the peach fruit fly. 2 4-DODECADIEN-1-OL plays a crucial role in research and applications related to insect behavior, mating, and population control strategies.

InChI:InChI=1/C12H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h8-11,13H,2-7,12H2,1H3/b9-8+,11-10+

Upstream product

• 3913-81-3 (E)-2-decenal 
• 24738-46-3 methyl (E,E)-dodeca-2,4-dienoate 
• 124-13-0 Octanal 
• 39924-20-4 (2E,4E)-dodecadien-2,4-oic acid ethyl ester 
• 67629-62-3 methyl 4-(diethylphosphono)crotonate 

Downstream Products

• 1379589-85-1 C₂₃H₃₄N₂O₃ 
• 1379591-08-8 C₂₅H₄₀N₂O₃ 
• 24738-48-5 2,4-dodecadienoic acid 
• 24738-51-0 (2E,4E)-N-isobutyldodeca-2,4-dienamide 
• 21662-16-8 trans,trans-2,4-dodecadienal 

Relevant articles and documents

Synthesis of (2E,4E)-dodeca-2,4-dien-1-yl isovalerate, the main component of rootstock oil of Echinacea purpurea

By phosphine-free Heck reaction a stereoselective synthesis was performed of (2E,4E)-dodeca-2,4-dien-1-yl isovalerate, the main component of the rootstock oil of Echinacea purpurea.

NOVEL 1,3-BENZOXAZOL-2(3H)-ONES AND THEIR USE AS MEDICAMENTS AND COSMETICS

The present invention relates to a novel class of 1,3-benzoxazol-2(3H) -ones of formula (1) and their use as a medicament, preferably as a dermatologic agent, and as a cosmetic. These novel compounds are particularly useful in treating and/or preventing inflammation, irritation, itching, pruritus, pain, oedema and/or pro-allergic or allergic conditions in a patient. Usually they are topically applied to the skin or mucosa in the form of a pharmaceutical or cosmetic composition comprising the compound and a pharmaceutically and/or cosmetically acceptable carrier.

NOVEL E,E-DIENE COMPOUNDS AND THEIR USE AS MEDICAMENTS AND COSMETICS

The present invention relates to a novel class of E,E-diene compounds and their use as a medicament, preferably as a dermatologic agent, and as a cosmetic. These novel compounds are particularly useful in treating and/or preventing inflammation, irritation, itching, pruritus, pain, oedema and/or pro-allergic or allergic conditions in a patient. Usually they are topically applied to the skin or mucosa in the form of a pharmaceutical or cosmetic composition comprising the compound and a pharmaceutically and/or cosmetically acceptable carrier.

Chiral aggregates formed from methylated tetraenoic fatty acids: Formation of both antipodes of chiral aggregates from a single enantiomer and time-dependent stereomutation

(Chemical Equation Presented) Formation and behaviors of chiral aggregates of methylated tetraenoic fatty acids (TE-FAs) were reported. In the C-24 TE-FA series, the aggregate prepared by dispersing an ethanol stock solution of C-24 TE-FA 1b into sodium phosphate buffer gave a strong positive Cotton effect, whereas the aggregate prepared from a methanol stock solution gave a negative Cotton effect. In the C-20 TE-FA series, the aggregate prepared from an ethanol stock solution of C-20 TE-FA 2b exhibited time-dependent chirality inversion.

Aggregation behavior of tetraenoic fatty acids in aqueous solution

(Chemical Equation Presented) Why so blue? Unique blue-shifted UV absorptions were used to follow the aggregation of C24 tetraene fatty acids in aqueous solution. Aggregation takes place through three distinct states (i.e. K→T1→T2; see picture). It is suggested that all of these aggregates are lamellar-type in a local sense but differ in the packing mode of the fatty acid backbone.

Copper(II) chloride dihydrate: A catalytic agent for the deprotection of tetrahydropyranyl ethers (THP ethers) and 1-ethoxyethyl ethers (EE ethers)

Tetrahydropyranyl ethers (THP groups) and 1-ethoxyethyl ethers (EE groups) are removed upon refluxing in 95% EtOH or Me2CO-H2O (95:5) in the presence of a catalytic amount of copper(II) chloride dihydrate (2-5 mol%).

Identification and synthesis of the sex pheromone of Phtheochroa cranaodes (Lepidoptera: Tortricidae)

The pheromone of Phtheochroa cranaodes (Lepidoptera: Tortricidae) was identified as (3E,5Z)-3,5-dodecadienyl acetate (5) by GC-MS analysis of female gland extracts and field trapping of males with synthetic compound.