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Home > Products >  1-Caprylene-3-alcoholCAS NO.: 3391-86-4

1-Caprylene-3-alcoholCAS NO.: 3391-86-4 CAS NO.3391-86-4

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Keywords

  • 1-Octen-3-ol
  • 1-OCTYLENE-3-OL
  • 1-OCTEN-3-OL

Quick Details

  • ProName: 1-Caprylene-3-alcoholCAS NO.: 3391-86-...
  • CasNo: 3391-86-4
  • Molecular Formula: C8H16O
  • Appearance: powder
  • Application: Synthetic fragrances
  • DeliveryTime: In stock
  • PackAge: drum
  • Port: China main port
  • ProductionCapacity: 10000 Gram/Day
  • Purity: 99%
  • Storage: Room temperature
  • Transportation: By sea or by air
  • LimitNum: 1 Gram
  • first class: 1-10

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Details

Product Name: 1-Octen-3-ol
Synonyms: 1-OCTEN-3-OL, (AMYL VINYL CARBINOL) FCC;1-OCTYLENE-3-OL;1-OCTEN-3-OL;AMYL VINYL CARBINOL (1-OCTEN 3-OL);1-OCTEN-3-OL 98+% FCC;n-Pentylvinylcarbinol;1-Octen-3-ol,98%;octenol,1-octen-3-ol
CAS: 3391-86-4
MF: C8H16O
MW: 128.21
EINECS: 222-226-0
Product Categories: -;API intermediates;alcohol Flavor;Flavors and Fragrances
Mol File: 3391-86-4.mol
1-Octen-3-ol Structure
 
1-Octen-3-ol Chemical Properties
Melting point  -49°C
Boiling point  84-85 °C25 mm Hg(lit.)
density  0.837 g/mL at 20 °C
vapor pressure  1 hPa (20 °C)
FEMA  2805 | 1-OCTEN-3-OL
refractive index  n20/D 1.437(lit.)
Fp  142 °F
storage temp.  Store below +30°C.
pka 14.63±0.20(Predicted)
form  Liquid
color  Clear colorless to pale yellow
Specific Gravity 0.84
explosive limit 0.9-8%(V)
Water Solubility  Not miscible or difficult to mix in water.
JECFA Number 1152
BRN  1744110
InChIKey VSMOENVRRABVKN-UHFFFAOYSA-N
CAS DataBase Reference 3391-86-4(CAS DataBase Reference)
NIST Chemistry Reference 1-Octen-3-ol(3391-86-4)
EPA Substance Registry System 1-Octen-3-ol (3391-86-4)
 
Safety Information
Hazard Codes  Xn
Risk Statements  22-36/38-20/21/22
Safety Statements  26-36
RIDADR  2810
WGK Germany  3
RTECS  RH3300000
Autoignition Temperature 245 °C
TSCA  Yes
HazardClass  6.1(b)
PackingGroup  III
HS Code  29052990
Toxicity LD50 orally in Rabbit: 340 mg/kg LD50 dermal Rabbit 3300 mg/kg
MSDS Information
Provider Language
1-Octen-3-ol English
SigmaAldrich English
ACROS English
ALFA English
 
1-Octen-3-ol Usage And Synthesis
Description 1-octen-3-ol, octenol (also known as mushroom alcohol) is a kind of secondary alcohol. It can emit special smell that can attract the biting insects such as mosquitoes. It is contained in the breath and sweat of mammals, and seems to be appreciated by insects such as mosquitoes. It is mainly produced by some plants and fungi including mushrooms and lemon balm through oxidative breakdown of linoleic acid. It can be used in combination with carbon dioxide to attract the insects to kill them. In addition, it can also be used as a food additive and used in certain perfumes. However, in animal study, it could disrupt dopamine homeostasis, and might be potentially involved in Parkinsonism.
Chemical Properties 1-Octen-3-Ol is a colorless to yellow liquid with a mushroom, green, vegetable, and fatty odor. It is used in edible flavor blends such as mushroom, tomato, potato, milk, and nut.It is a secondary alcohol derived from 1-octene. It is an unsaturated alcohol that exists as two enantiomers, the (R)-(–)-form and the (S)-(+)-form. It is found most often as the racemic mixture.
Common Applications
  • cheese
  • lavender
  • potato
  • savoury
  • asparagus
  • carrot
  • cucumber
  • mushroom
Natural occurrence: Clover, cooked artichoke, fish, mushroom, peas, soybeans, wheat bread, tea, and beef.
Uses
  1. 1-Octen-3-ol is a chemical that attracts biting insects such as mosquitoes. It occurs naturally in some plants, fungi, and molds; and it is a metabolite of linoleic acid. It is also found in human breath and sweat, which is unfortunate because it attracts mosquitoes and other biting insects and it was once believed that insect repellent DEET works by blocking the insects' octenol odorant receptors.
  2. Used as a flavoring agent in cheese and chocolate.
  3. Used as a perfuming agent in cosmetic industry.
  4. Since the discovery in the early 1980s that 1-octen-3-ol, isolated from oxen breath, attracts tsetse fly, there has been growing interest in exploring the use of this semiochemical as a possible generic lure for trapping host-seeking mosquitoes. Intriguingly, traps baited with 1-octen-3-ol captured significantly more females of the malaria mosquito, Anopheles gambiae, and the yellow fever mosquito, Aedes aegypti, than control traps, but failed to attract the southern house mosquito, Culex quinquefasciatus.
References
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Description l-Octen-3-ol has a powerful, sweet, earthy odor with a strong, herbaceous note reminiscent of lavender-lavandin, rose, and hay. It has a sweet, herbaceous taste. May be prepared from magnesium amyl bromide and acrolein.
Chemical Properties 1-Octen-3-ol has a powerful, sweet, earthy odor with a strong, herbaceous note reminiscent of lavender–lavandin, rose and hay. It has a sweet, herbaceous taste.
Chemical Properties 1-Octen-3-ol may occur in the optically active form. It is found, for example, in lavender oil and is a steam-volatile component of mushrooms. l-Octen-3-ol is a liquid with an intense mushroom, forest–earthy odor that can be prepared by a Grignard reaction from vinylmagnesium bromide and hexanal. It is used in lavender compositions and in mushroom aromas.
Occurrence Originally reported found in the mushroom Armillaria matsutake, a parasite growing on the radical hairs of Pinus densiflora in the forests of Japan; it has been isolated also in the essential oils of Mentha pulegium L., lavender and Mentha timjia. Also reported found in over 160 foods and beverages including banana, kumquat peel oil, berries, currants, guava, grapes, raisin, melon, pineapple, asparagus, potato, tomato, Mentha oils, thyme, wheat bread, cheeses, buttermilk, boiled egg, fish, cooked meats, hop oil, beer, cognac, rum, grape wines, cocoa, coffee, tea, pecans, plum, oats, soybean, olive, cloudberry, plums, beans, mushroom, marjoram, starfruit, sesame seed, fig, kelp, rice, beans, litchi, calamus, dill, licorice, pumpkin, buckwheat, sweet corn, corn tortilla, malt, rice, wort, krill, rosemary, Bourbon vanilla, mountain papaya, endive, lemon balm, shrimp, oyster, crab, clam, scallop, truffle, winter savory, anise hyssop and maté.
Preparation From magnesium amyl bromide and acrolein.
Definition ChEBI: An alkenyl alcohol with a structure based on a C8 unbranched chain with the hydroxy group at C-2 and unsaturation at C-11C-2.
Aroma threshold values Detection: 14 ppb; recognition: 25 ppb
Taste threshold values Taste characteristics at 10 ppm: mushroom, earthy, fungal, green, oily, vegetative, umami sensation and savory-brothy.
Trade name Matsutakeol (Takasago).
Safety Profile Poison by ingestion and intravenous routes. Moderately toxic by skin contact. When heated to decomposition it emits acrid smoke and irritating fumes.

 

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