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Merck

74900

Supelco

1-Octen

analytical standard

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About This Item

Lineare Formel:
CH3(CH2)5CH=CH2
CAS-Nummer:
Molekulargewicht:
112.21
Beilstein:
1734497
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Dampfdichte

3.9 (vs air)

Dampfdruck

36 mmHg ( 38 °C)

Assay

≥99.5% (GC)

Selbstzündungstemp.

446 °F

Haltbarkeit

limited shelf life, expiry date on the label

Expl.-Gr.

3.9 %

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

n20/D 1.408 (lit.)
n20/D 1.408
n20/D 1.409 (lit.)

bp

122-123 °C (lit.)

mp (Schmelzpunkt)

−101 °C (lit.)

Dichte

0.715 g/mL at 25 °C (lit.)

Anwendung(en)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care
petroleum

Format

neat

SMILES String

CCCCCCC=C

InChI

1S/C8H16/c1-3-5-7-8-6-4-2/h3H,1,4-8H2,2H3

InChIKey

KWKAKUADMBZCLK-UHFFFAOYSA-N

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Allgemeine Beschreibung

1-Octene is a linear α-olefin and an important comonomer in the production of linear low-density polyethylene (LLDPE).
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signalwort

Danger

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2

Zusätzliche Gefahrenhinweise

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

50.0 °F - closed cup

Flammpunkt (°C)

10 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Analysenzertifikate (COA)

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Slide 1 of 5

1 of 5

Ethylene tetramerization: a new route to produce 1-octene in exceptionally high selectivities
Bollmann A, et al.
Journal of the American Chemical Society, 126(45), 14712-14713 (2004)
J C Quada et al.
Bioorganic & medicinal chemistry, 9(9), 2303-2314 (2001-09-13)
The syntheses of several novel halogenated bithiazoles structurally related to the bithiazole moiety of bleomycin A(5) are described. Also described is the ability of these compounds to mediate photoactivated DNA cleavage. Chlorinated bithiazole analogues were shown to be much more
Frans T I Marx et al.
Journal of molecular modeling, 15(11), 1371-1381 (2009-06-02)
The productive self-metathesis reaction of 1-octene in the presence of the Phobcat precatalyst [RuCl(2)(Phoban-Cy)(2)(=CHPh)] using density functional theory was investigated and compared to the Grubbs 1 precatalyst [RuCl(2)(PCy(3))(2)(=CHPh)]. At the GGA-PW91/DNP level, the geometry optimization of all the participating species
F P Guengerich
Biochemical and biophysical research communications, 138(1), 193-198 (1986-07-16)
The heme in rat liver microsomal cytochrome P-450 was labeled with 14C or 3H and the microsomes were fractionated after in vitro incubations with a variety of agents known to destroy cytochrome P-450 heme. A major fraction of the heme
I N White et al.
Biochemical pharmacology, 35(9), 1569-1575 (1986-05-01)
The enzymic activation of a model olefin oct-1-ene was studied in rat liver microsomal systems in vitro. An active metabolite was trapped using N-acetylcysteine and identified by means of capillary GLC/mass spectrometry and 360 MHz 1H NMR as S-3-oxo-octyl-N-acetylcysteine. A

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