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W429300 Aldrich

1-Octene

98%

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Properties

Related Categories Alphabetical Listings, Flavors and Fragrances, O-P More...
biological source   synthetic
vapor density   3.9 (vs air)
vapor pressure   36 mmHg ( 38 °C)
assay   98%
autoignition temp.   446 °F
expl. lim.   3.9 %
refractive index   n20/D 1.408(lit.)
  n20/D 1.409(lit.)
bp   122-123 °C(lit.)
mp   −101 °C(lit.)
density   0.715 g/mL at 25 °C(lit.)
Organoleptic   camphoraceous
allergen   no known allergens

Description

Packaging

1 kg in poly bottle

5 kg in steel drum

Price and Availability

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analytical standard

1-Octene

purum, ≥97.0% (GC)

Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
Hazard statements 
Precautionary statements 
Supplemental Hazard Statements 
Repeated exposure may cause skin dryness or cracking.
Hazard Codes (Europe) 
Risk Statements (Europe) 
Safety Statements (Europe) 
60-61-62
RIDADR 
UN 3295 3/PG 2
WGK Germany 
1
Flash Point(F) 
50 °F
Flash Point(C) 
10 °C

Protocols & Articles

Peer-Reviewed Papers

References

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High-precision catalysts: regioselective hydroformylation of internal alkenes by encapsulated rhodium complexes. Kuil M, Soltner T, van Leeuwen PW, et al. J. Am. Chem. Soc. 128(35), 11344-5, (2006)

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Does Haber's law apply to human sensory irritation? Shusterman D, Matovinovic E, and Salmon A Inhal. Toxicol. 18(7), 457-71, (2006)

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Cooperative ligand effects in phase-switching homogeneous catalysts. Mokhadinyana M, Desset SL, Williams DB, et al. Angew. Chem. Int. Ed. Engl. 51(7), 1648-52, (2012)

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Products and mechanisms of the gas-phase reactions of OH radicals with 1-octene and 7-tetradecene in the presence of NO. Aschmann SM, Tuazon EC, Arey J, et al. Environ. Sci. Technol. 44(10), 3825-31, (2010)

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Aqueous-phase hydroformylation of 1-octene: styrene latices as phase-transfer agents. Kunna K, Müller C, Loos J, et al. Angew. Chem. Int. Ed. Engl. 45(43), 7289-92, (2006)

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Time course of sensory eye irritation in humans exposed to N-butanol and 1-octene. Hempel-Jørgensen A, Kjaergaard SK, Môlhave L, et al. Arch. Environ. Health 54(2), 86-94, (1999)

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Catalytic conversion of bio-oil to oxygen-containing fuels by simultaneous reactions with 1-butanol and 1-octene over solid acids: Model compound studies and reaction pathways. Zhang ZJ, Sui SJ, Tan S, et al. Bioresour. Technol. 130, 789-92, (2013)

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Behavior of some solid food simulants in contact with several plastics used in microwave ovens. Nerín C and Acosta D J. Agric. Food Chem. 50(25), 7488-92, (2002)

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An improved procedure for the purification of catalytically active alkane hydroxylase from Pseudomonas putida GPo1. Xie M, Alonso H, and Roujeinikova A Appl. Biochem. Biotechnol. 165(3-4), 823-31, (2011)

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Covalent binding to apoprotein is a major fate of heme in a variety of reactions in which cytochrome P-450 is destroyed. Guengerich FP Biochem. Biophys. Res. Commun. 138(1), 193-8, (1986)

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Isolation and functional analysis of cytochrome P450 CYP153A genes from various environments. Kubota M, Nodate M, Yasumoto-Hirose M, et al. Biosci. Biotechnol. Biochem. 69(12), 2421-30, (2005)

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A cartridge system for organometallic catalysis: sequential catalysis and separation using supercritical carbon dioxide to switch phases. Solinas M, Jiang J, Stelzer O, et al. Angew. Chem. Int. Ed. Engl. 44(15), 2291-5, (2005)

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Aqueous-phase hydroformylation of 1-octene using hydrophilic sulfonate salicylaldimine dendrimers. Hager EB, Makhubela BC, and Smith GS Dalton Trans. 41(45), 13927-35, (2012)

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Photoactivated DNA cleavage by compounds structurally related to the bithiazole moiety of bleomycin. Quada JC, Boturyn D, and Hecht SM Bioorg. Med. Chem. 9(9), 2303-14, (2001)

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Tests of potential functional barriers for laminated multilayer food packages. Part I: Low molecular weight permeants. Simal-Gándara J, Sarria-Vidal M, Koorevaar A, et al. Food Addit. Contam. 17(8), 703-11, (2000)

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DFT investigation of the 1-octene metathesis reaction mechanism with the Phobcat precatalyst. Marx FT, Jordaan JH, and Vosloo HC J. Mol. Model. 15(11), 1371-81, (2009)

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Optimisation of polystyrene resin-supported Pt catalysts in room temperature, solvent-less, oct-l-ene hydrosilylation using methyldichlorosilane. Drake R, Dunn R, Sherrington DC, et al. Comb. Chem. High Throughput Screen 5(3), 201-9, (2002)

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Immobilization of microbial cells in a mixed matrix of silicone polymer and calcium alginate gel: epoxidation of 1-octene by Nocardia corallina B-276 in organic media. Kawakami K, Tsuruda S, and Miyagi K Biotechnol. Prog. 6(5), 357-61, (1990)

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Stereochemistry of cytochrome P-450-catalyzed epoxidation and prosthetic heme alkylation. Ortiz de Montellano PR, Mangold BL, Wheeler C, et al. J. Biol. Chem. 258(7), 4208-13, (1983)

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Influence of nanopores of MCM-41 and SBA-15 confining (n-BuCp)2ZrCl2 on copolymerization of ethylene-alpha-olefin. Y. S. Ko, et al., J. Nanosci. Nanotechnol. 10, 180-185, (2010)

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Rh nanoparticle catalyzed hydroaminomethylation of 1-octene in thermoregulated ionic liquid and organic biphasic system. Xu Y, Wang Y, Li K, et al. J. Nanosci. Nanotechnol. 13(7), 5048-52, (2013)

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Nanolithography based on the formation and manipulation of nanometer-size organic liquid menisci. Martinez RV and Garcia R Nano Lett. 5(6), 1161-4, (2005)

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Metabolic activation of olefins. Conversion of 1-octene to a putative reactive intermediate 1-octen-3-one: an alternative pathway to epoxidation. White IN, Green ML, Bailey E, et al. Biochem. Pharmacol. 35(9), 1569-75, (1986)

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Merck 14,1764

Beil. 1,IV,874

Aldrich MSDS 1, 1405:B / Corp MSDS 1 (2), 2645:B / FT-IR 1 (1), 14:A / FT-IR 2 (1), 25:B / FT-NMR 1 (1), 18:C / IR-Spectra (2), 10:F / IR-Spectra (3), 10:G / NMR-Reference 2 (1), 20:D / RegBook 1 (1), 15:G / Sigma FT-IR 1 (2), 810:A / Structure Index 1, 2:A:6 / Vapor Phase 3, 19:A

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