Molecular Formula | C10H16O |
Molar Mass | 152.23 |
Density | d420 0.8860 |
Boling Point | bp2.6 91-92° |
Water Solubility | 289mg/L(25 ºC) |
Refractive Index | nD20 1.4869 |
Physical and Chemical Properties | EPA Chemical Information 2,6-Octadienal, 3,7-dimethyl-, (2Z)- (106-26-3) |
UN IDs | 1760 |
Hazard Class | 8 |
Packing Group | III |
Raw Materials | (2Z)-3,7-Dimethyl-2,6-octadienoic acid NEROL |
Downstream Products | 2,6-Octadienoic acid, 3,7-dimethyl-, (E)- (+)-CITRONELLAL (-)-CITRONELLAL |
(Z) 3,7-dimethyl-2,6-octadienal is an organic compound, and the following is an introduction to its properties, uses, preparation methods, and safety information:
nature:
1. It is a colorless liquid with a unique aromatic odor.
2. Soluble in various organic solvents such as ethanol, ether, and chlorinated hydrocarbons.
Manufacturing method:
1. Produced through the oxidation reaction of styrene.
2. A common preparation method is to expose styrene to oxygen and add appropriate catalysts such as palladium, platinum, or cobalt.
Security information:
1. It is generally safe under normal usage conditions.
2. It may be irritating to the human body and should be avoided from contact with the skin and eyes.
3. Suitable protective equipment such as gloves and goggles should be worn during use.
4. It should be stored away from sources of fire and flammable materials, and ensure that the storage container is well sealed.
5. If accidentally swallowed or inhaled, please seek medical assistance immediately.
FEMA | 2303 | CITRAL |
add (z)-3,7-dimethyl -2,6-octadiene -1-alcohol (nerol)(2)5.7mL(32.5mmol), acetonitrile 28mL,PH7 buffer 8mL (purchased from Fluka company),2,2,6,6-tetramethylpiperidine oxide (TEMPO)490mg(3.24mmol) into the reaction bottle equipped with a stirrer, iodobenzene diacetate 11.49g(35.71mmol). The reaction was stirred at 0 ℃ until TLC detection no longer showed the raw material absorption spots of nerol (the reaction went on very quickly, and the reaction basically ended in about 20min). Add 100mL of ether, transfer into a separatory funnel, and wash twice with sodium thiosulfate solution. The organic layer is separated, and the water layer is extracted 3 times with ether. The organic layers are combined and washed with saturated sodium bicarbonate and saturated brine in turn. Anhydrous sodium sulfate is dried, filtered, solvent is distilled under reduced pressure, the residue is purified by silica gel column, ether-hexane (1:9) is eluted, and finally colorless oily liquid (1) ① 4.30~4.39g is obtained with a yield of 87% ~ 89%.