1-OCTENE CAS Number: 111-66-0

Product 1-OCTENE
CAS 111-66-0
MF C8H16
Formula Octene-1 (99%;1-OCTENE, 1000MG, NEAT;1-OCTENE, STANDARD FOR GC;Octene, linear;1-Octene, 99+%;1-N-OCTENE;n-Octen-1;OCTEN-1

product description

Basic Info.

Model NO. : 111-66-0
EINECS : 203-896-3
Source : Ester & Derivative
Appearance : Liquid
Grade Standard : Industrial Grade
Colour : Transparent
Sample : Available
Storage : Cool Place
Moisture : ≤0.2
Purity : 99.5%Min
Shelf Life : 24 Months
Transport Package : Steel Drums, IBC Totes, Customized
Trademark : ACF
Origin : China
Production Capacity : 20000 Tons/Year

1-OCTENE Properties

Melting point -101 °C (lit.)
Boiling point 122-123 °C (lit.)
Density 0.715 g/mL at 25 °C (lit.)
vapor density 3.9 (vs air)
vapor pressure 36 mm Hg ( 38 °C)
refractive index n20/D 1.408(lit.)
FEMA 4293 | 1-OCTENE
Flash point 70 °F
storage temp. Store below +30°C.
solubility Soluble in acetone, benzene, and chloroform (Weast, 1986). Miscible with alcohol, ether (Windholz et al., 1983), and many aliphatic hydrocarbons.
form Liquid
pka >14 (Schwarzenbach et al., 1993)
color Clear
Specific Gravity 0.714
Odor gasoline
Odor Threshold 0.001ppm
biological source synthetic
Viscosity 0.66mm2/s
explosive limit 0.7-6.8%(V)
Water Solubility Miscible with water, ether, alcohol and acetone.
Merck 14,1764
JECFA Number 2191
BRN 1734497
Henry’s Law Constant 0.952 at 25 °C (Hine and Mookerjee, 1975)
Dielectric constant 2.1(20℃)
Stability Stable. Highly flammable. Incompatible with strong oxidizing agents, acids.
Major Application cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care
petroleum
Cosmetics Ingredients Functions SOLVENT
InChI 1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3
InChIKey KWKAKUADMBZCLK-UHFFFAOYSA-N
SMILES CCCCCCC=C
LogP 4.47 at 20℃
CAS DataBase Reference 111-66-0(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) 1-OCTENE
FDA UNII E5VK21B9RC
EPA Substance Registry System 1-Octene (111-66-0)
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS08,GHS09
Signal word Danger
Hazard statements H225-H304-H410
Precautionary statements P210-P233-P240-P273-P301+P310-P331
PPE Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes F,Xn,N
Risk Statements 11-51/53-65-10-66-50/53-38
Safety Statements 16-60-62-61
RIDADR UN 3295 3/PG 2
WGK Germany 1
RTECS RH2207000
Autoignition Temperature 446 °F
TSCA TSCA listed
HazardClass 3
PackingGroup II
HS Code 29012990
Storage Class 3 – Flammable liquids
Hazard Classifications Aquatic Acute 1
Aquatic Chronic 1
Asp. Tox. 1
Flam. Liq. 2
Hazardous Substances Data 111-66-0(Hazardous Substances Data)
Toxicity LD50 orally in Rabbit: > 5000 mg/kg LD50 dermal Rabbit > 2000 mg/kg
Limited Quantities 1.0 L (0.3 gallon) (liquid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)

1-OCTENE Chemical Properties,Uses,Production

Chemical Properties

colourless liquid

Chemical Properties

Colorless, clear liquid; gasoline aroma.

Physical properties

Clear, colorless, flammable liquid with a mild but unpleasant hydrocarbon odor. Based on a triangle bag odor method, an odor threshold concentration of 1.0 ppbv was reported by Nagata and Takeuchi (1990).

Uses

Plasticizer; surfactants. Used as a comonomer in the production of high density polyethylene and linear low density polyethylene. Starting material for synthesis of a variety of compounds including nananoic acid.

Uses

1-Octene acts as a comonomer used in the preparation of polyethylene, especially high-density polyethylene (HDPE) and linear low-density polyethylene(LLDPE) resins. It is also used in organic synthesis, surfactants and plasticizers. Further, it is used in process regulators and viscosity adjustors. In addition to this, it is used in the preparation of linear aldehyde through the oxo synthesis (hydroformylation) to get the nonanal.

Uses

1-Octene is a linear α-olefin mainly used as a comonomer in the synthesis of linear low-density polyethylene (LLDPE). Extensive work has been reported on the hydroformylation of 1-octene using various catalysts. It is also an important source to synthesize important petrochemical building blocks via epoxidation reaction.

Production Methods

Production method: 1) from Allyl chloride and n-Amyl magnesium bromide. 2) from Octanol with Iodine and red phosphorus. 3) from Monosodium acetylene with Octyl iodide in liquid Ammonia at 40” C. under pressure.

Definition

ChEBI: An octene with an unsaturation C-1.

Aroma threshold values

High strength odor; recommend smelling in a 1.00% solution or less.

Synthesis Reference(s)

Journal of the American Chemical Society, 93, p. 1487, 1971 DOI: 10.1021/ja00735a030
Tetrahedron Letters, 25, p. 1283, 1984 DOI: 10.1016/S0040-4039(01)80135-0

General Description

A colorless liquid. Flash point 70°F. Insoluble in water and less dense (at about 6 lb / gal) than water. Hence floats on water. Vapors are heavier than air and may settle in depressions. Reported to biodegrade very slowly. Used in organic synthesis, surfactants, and plasticizers.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

1-OCTENE may react vigorously with strong oxidizing agents. May react exothermically with reducing agents to release hydrogen gas. In the presence of various catalysts (such as acids) or initiators, may undergo exothermic addition polymerization reactions.

Health Hazard

Generally low toxicity. Mildly anesthetic at high vapor concentrations. May irritate eyes.

Source

Identified as one of 140 volatile constituents in used soybean oils collected from a processing plant that fried various beef, chicken, and veal products (Takeoka et al., 1996).

Environmental Fate

Biological. Biooxidation of 1-octene may occur yielding 7-octen-1-ol, which may oxidize to 7- octenoic acid (Dugan, 1972).
Photolytic. Atkinson and Carter (1984) reported a rate constant of 8.1 x 10-18 cm3/molecule?sec for the reaction of 1-octene and OH radicals in the atmosphere.
Chemical/Physical. The reaction of ozone and OH radicals with 1-octene was studied in a flexible outdoor Teflon chamber (Paulson and Seinfeld, 1992). 1-Octene reacted with ozone producing heptanal, a thermally stabilized C7 biradical, and hexane at yields of 80, 10, and 1%, respectively. With OH radicals, only 15% of 1-octene was converted to heptanal. In both reactions, the remaining compounds were tentatively identified as alkyl nitrates (Paulson and Seinfeld, 1977). Grosjean et al. (1996) investigated the atmospheric chemistry of 1-octene with ozone and an ozone-nitrogen oxide mixture under ambient conditions. The reaction of 1-octene and ozone in the dark yielded formaldehyde, hexanal, heptanal, cyclohexanone, and a compound tentatively identified as 2-oxoheptanal. The sunlight irradiation of 1-octene with ozone-nitrogen oxide yielded the following carbonyls: formaldehyde, acetaldehyde, propanal, 2-butanone, butanal, pentanal, glyoxal, hexanal, heptanal, and pentanal.
Chemical/Physical. Complete combustion in air yields carbon dioxide and water.

Purification Methods

Distil 1-octene under nitrogen from sodium which removes water and peroxides. Peroxides can also be removed by percolation through dried, acid washed, alumina. Store it under N2, or Ar in the dark. [Strukul & Michelin J Am Chem Soc 107 7563 1985, Beilstein 1 H 221, 1 II 199, 1 IV 874.]

629-05-0
111-66-0
Synthesis of 1-OCTENE from 1-Octyne

1-OCTENE Preparation Products And Raw materials

FAQ

 

Q1: About the after-sale service of products
A: After purchasing the products from our factory, we have A professional technical team and after-sales team to serve you and solve all your problems in the future.

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Q5: What is your MOQ?
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But usually we can accept a smaller quantity, say 100g, at the cost of 100% sample charge.

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             ACF Chemical Co., Ltd.

Leon 

phone/whatsapp:008615950692266

email:md@acfchemical.com

No. 45 Pengwan Road, Qianwan Bonded Port Area, Qingdao Area, China (Shandong)
welcome to vist our factory.
sample is free
ACF Chemical Qingdao Co., Ltd. was established in 1987. the company has over decades of experience in the production of methacrylate and acrylate series products, as well as high-efficiency polymerization inhibitors and rubber and plastic antioxidant series products. The company’s leading products are high-efficiency polymerization inhibitor series products, with an annual production capacity of 1,000 tons of tert-butylhydroquinone (TBC), 800 tons of polymerization inhibitor TH-701, 500 tons of polymerization inhibitor TH-A294, 500 tons of polymerization inhibitor TH-100BE, 500 tons of phenothiazine, and 200 tons of hydroquinone.

DMEA 108-01-0
Dodecyl trimethyl ammonium chloride 112-00-5
N-Hexadecyltrimethylammonium chloride 112-02-7
1831 112-03-8
1631Br 57-09-0
D821 5538-94-3
D8/1021 68424-95-3
D1021 7173-51-5
D1821 61789-80-8
TEP88 157905-74-3
1227 C12 139-07-1
DMPT(N,N-Dimethyl-p-toluidine) 99-97-8
NDPT(N,N-dihydroxyethyl-p-toluidine) 3077-12-1.
DMA(N,N-dimethylaniline) 121-69-7
N,N-Diethylaniline 91-66-7
MT(M-Toluidine) 108-44-1
PT(P-Toluidine) 106-49-0
O-Toluidine  OT 95-53-4
Dimethyl(octyl)amine 7378-99-6/1120-24-7
C16-18-alkyldimethyl   Octadecyl/Hexadecyl dimethylamines 68390-97-6
Octadecyl/behenyl dimethylamines 124046-42-0
N,N-dimethyldocosylamine 21542-96-1
N-Methyldioctylamine 4455-26-9
Di(octyl/decyl) methylamines 308062-61-5
Didecyl methylamine 7396-58-9
N-methyldidodecylamine 2915-90-4
Dipalmitamine 16724-61-1
Trioctylamine 1116-76-3
Trioctylamine 68814-95-9
N-3-Laurylamidopropyl dimethylamine 3179-80-4
N-3-(Hydrogenated cocoamido)propyl dimethylamines 288095-05-6
N-3-Oleylamidopropyl dimethylamine 109-28-4
N-3-Erucylamidopropyl dimethylamine 60270-33-9
N-Oleyl 1,3-propanediamine 7173-62-8
Bis(aminopropyl)laurylamine 2372-82-9
N-tallow alkyltripropylenetetra 68911-79-5
3-(isodecyloxy)propylamine 30113-45-2
N-[3-(isodecyloxy)propyl]propane-1,3-diamine 72162-46-0
2-(Methylamino)ethanol 109-83-1
N-Methyldiethanolamine 105-59-9
3-Methoxy propyl amine 5332-73-0
N,N-dimethylcyclohexylamine 98-94-2
1,3,5-Tris[3-(dimethylamino)propyl]hexahydro-1,3,5-triazine 15875-13-5
N,N,N’-trimethylamino-N’-ethylethanolamine 2212-32-0
N,N-Dimethylethanolamine 108-01-1
Acetone
Acrylic acid
Adipic acid
Alpha-Methylstyrene (AMS)
Benzoic Acid
Bisphenol A
Butyl Acrylat (BA)
Butyl acetate (Butac)
Butyl diglycol (BDG)
Butyl glycol
Para-tertiary butyl benzoic acid (PTBBA)
n-Butanol
n-Butyl methacrylate (n-BUMA)
para-tert. Butylphenol (PTBP)

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