trans-2-Hexene, 99%
trans-2-Hexene, 99%
trans-2-Hexene, 99%
Thermo Scientific Chemicals

trans-2-Hexene, 99%

CAS: 4050-45-7 | C6H12 | 84.16 g/mol
製品番号(カタログ番号) B22289.88
または、製品番号B22289-88
価格(JPY)
-
数量:
2.5 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS4050-45-7
IUPAC Name(2E)-hex-2-ene
Molecular FormulaC6H12
InChI KeyRYPKRALMXUUNKS-HWKANZROSA-N
SMILESCCCC=CC
さらに表示
Appearance (Color)Clear colorless
Assay (GC)≥98.5%
FormLiquid
Refractive Index1.3925-1.3955 @ 20?C
Identification (FTIR)Conforms
trans-2-Hexene is used as a co monomer in the production of polyethylene. The use of trans-2-hexene, which is derived from 3-hexyne using sodium in liquid ammonia.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
trans-2-Hexene is used as a co monomer in the production of polyethylene. The use of trans-2-hexene, which is derived from 3-hexyne using sodium in liquid ammonia.

Solubility
Difficult to mix.

Notes
Store away from strong oxidizing agents. Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only

General References:

  1. J. Abbot.; B.W. Wojciechowski. The nature of active sites in the isomerization of 1-hexene on cracking catalysts. Journal of Catalysis. 1984, 90, (2), 270-278.
  2. Cheal Kim.; Kui Chen.; Jinheung Kim.; Lawrence Que , Jr. Stereospecific Alkane Hydroxylation with H2O2 Catalyzed by an Iron(II)-Tris(2-pyridylmethyl)amine Complex. J. Am. Chem. Soc. 1997, 119, (25), 5964-5965.