Odowell is a professional 2-octanone manufacturers and 2-octanone suppliers in China . Odowell is ploughing in Flavors & Fragrances industry since 2012, constantly R&D new raw materials and new technology to fulfill perfumers and flavorists’ growing pursuit of product variety and quality. Our 2-octanone cas 111-13-7 have a good price advantage, premium quality with liquid appearance, production capacity of 150 tons per year and popular in European and American markets.
2-Octanone is used in perfumes, high-boiling solvent, especially for epoxy resin coatings and in leather finishes. It is used in flavoring, odorant. It can act as antiblushing agent for nitrocellulose lacquers. 2-Octanone may be used as an analytical reference standard for the quantification of the analyte in sugar-cane spirits and rum samples and whey protein concentrate using chromatography based techniques.
Reported found in apple, apricot, banana, cranberry, grape, raisin, papaya, peach, raspberry, strawberry, leek, peas, clove, wheat bread, many cheeses, butter, milk, cooked egg, yogurt, caviar, fatty fish, meats, beer, hop oil beer, cognac, rum, grape wines, cocoa, coffee, tea, roasted filberts and peanuts, pecans, potato chips, oats, soybean, olive, beans, walnut, trassi, mushroom, fig, rice, buckwheat, quince, sweet corn, corn oil, malt, wort, krill, Bourbon vanilla, mountain papaya, shrimp, crab, crayfish, clam, truffle, maté and mastic gum oil.
2-octanone Cas 111-13-7
2-Octanone is also Methyl n-hexyl ketone. 2-Octanone has a floral and bitter, green, fruity (unripe apple) odor with a bitter camphoraceous taste. May be synthesized by the oxidation of methyl hexyl carbinol with K2Cr2O7 and sulfuric acid; also by oxidation of 2-octanol over zinc oxide at 330 - 340°C. It’s a colorless liquid; pleasant odor; cam-phor taste. Insoluble in water; solublein alcohol, hydrocarbons, ether, esters, etc. Com-bustible.
2-Octanone can be produced by oxidation of methyl hexyl carbinol, 2-octanol, or 1-octene or by reductive condensation of acetone with pentanol. Commercial samples can have a purity of 98%.
Premium quality 2-Octanone with clear colorless liquid appearance, Odowell 2-Octanone with high quality in stock and free Sample for testing. Production capacity: 150 Tons annually manufacturing for European countries and American market.
2-Octanone (Specification)
Product Name: |
2-Octanone |
Synonyms: |
femanumber2802;n-C6H13COCH3;octan-2-;Octan-2-one;2-OCTANONE 98+% FCC;2-OCTANONE OEKANAL;2-OCTANONE REAGENT GRADE 98%;2-OCTANONE, STANDARD FOR GC |
CAS: |
111-13-7 |
MF: |
C8H16O |
MW: |
128.21 |
EINECS: |
203-837-1 |
Product Categories: |
|
Mol File: |
111-13-7.mol |
2-Octanone Feature And Application
2-Octanone is a volatile flavor compound reported to be found in blue cheese, acerola fruit, blue crab and cray fish. c is a kind of natural ketone found in many sources such as coco, baked peanuts, potato, cheese, beer, banana and oranges. It can be used as a flavor and fragrance ingredient. It is used in the field of fiber, medicine, pesticides and spices for the synthesis of fiber oil, defoamer and the preparation of surfactants, coal flotation agent.
Methyl n-hexyl ketone is used as solvent for vinyl compounds and dyes and is suitable for dispersing dyes in light-weight petroleum oils for newsprint inks. Poison by ingestion. Moderately toxic by intraperitoned route. A sktn irritant. Flammable liquid when exposed to heat, flame, or oxidizers. To fight fire, use foam, alcohol foam. When heated to decomposition it emits acrid smoke and irritating fumes. See also ETHER and KETONES.
2-octanone Details
1-Octyne (7.5 g) and formic acid (100 mL) were heated in an oil bath at 100 ºC until all starting material was consumed. The progress of the reaction was monitored by GC analysis of the reaction solution. Quantitative GC analysis at the end of the reaction (6 h) indicated 92% yield of 2-octanone. The cooled reaction mixture was taken up with CH2Cl2 (170 mL), and the solution was washed with water, sodium carbonate solution, and water, dried over MgSO4, and evaporated in vacuo. The residue was distilled (bp 171–173 ºC) to give 2-octanone (7.42 g, 85%).
Reference: Menashe, N.; Reshef, D.; Shvo, Y. J. Org. Chem. 1991, 56, 2912–2914.
Chemical Properties
Melting point |
-16 °C |
Boiling point |
173 °C(lit.) |
density |
0.819 g/mL at 25 °C(lit.) |
vapor pressure |
1.8-2.614hPa at 20-25℃ |
FEMA |
2802 | 2-OCTANONE |
refractive index |
n20/D 1.416(lit.) |
Fp |
133 °F |
storage temp. |
Sealed in dry,2-8°C |
solubility |
0.9g/l |
form |
Liquid |
color |
Clear colorless to very slightly yellow |
Odor |
at 10.00 % in dipropylene glycol. earthy weedy natural woody herbal |
Odor Type |
earthy |
Water Solubility |
0.9 g/L |
Merck |
14,4711 |
JECFA Number |
288 |
BRN |
635843 |
Stability: |
Stable. Incompatible with strong oxidizing agents. Flammable. |
LogP |
1.95-2.37 at 25℃ |
CAS DataBase Reference |
111-13-7(CAS DataBase Reference) |
NIST Chemistry Reference |
2-Octanone(111-13-7) |
EPA Substance Registry System |
2-Octanone (111-13-7) |
Safety Information
Hazard Codes |
Xn |
Risk Statements |
21-10 |
Safety Statements |
36/37-16 |
RIDADR |
UN 1224 3/PG 3 |
WGK Germany |
1 |
RTECS |
RH1484000 |
TSCA |
Yes |
HazardClass |
3 |
PackingGroup |
III |
HS Code |
29141990 |
Hazardous Substances Data |
111-13-7(Hazardous Substances Data) |
toxicity |
Both the acute oral LD50 in rats and the acute dermal LD50 in rabbits exceeded 5 g/kg (Moreno, 1973). |
Quality Certificates
Our company meet the highest quality requirements as stipulated in ISO9001.