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Merck
CN

377171

1,2-环氧己烷

97%

别名:

1-己烯氧化物, 丁基环氧乙烷

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关于此项目

经验公式(希尔记法):
C6H12O
化学文摘社编号:
分子量:
100.16
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
215-864-6
Beilstein/REAXYS Number:
102568
MDL number:
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产品名称

1,2-环氧己烷, 97%

InChI key

WHNBDXQTMPYBAT-UHFFFAOYSA-N

InChI

1S/C6H12O/c1-2-3-4-6-5-7-6/h6H,2-5H2,1H3

SMILES string

CCCCC1CO1

assay

97%

form

liquid

impurities

<3% acetic acid

refractive index

n20/D 1.406 (lit.)

bp

118-120 °C (lit.)

density

0.831 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

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Application

  • 聚(环氧氯丙烷-co-1, 2-环氧己烷)–一种前景良好的用于叠氮聚合物成型固化(cast-cure)的前体:讨论了采用环氧氯丙烷和1, 2-环氧己烷合成的一种共聚物,研究目的在于开发一种用于能量应用的内增塑剂(TM Klapötke, 2016)。
  • 以小晶体合成的多级孔沸石(hierarchically porous zeolite) TS-1 及其1-己烯环氧化反应性能:该研究考察了1, 2-环氧己烷在各种化学行业用中间体制备中的催化性能(M Zhang et al., 2021)。
  • 利用来自红球菌 ST‐10(RhSMO)的苯乙烯单加氧酶进行手性环氧烷烃的生物生产:关注了利用生物催化剂进行(S)-1,2-环氧己烷的酶法生产,重点介绍了其在手性环氧烷烃制备中的潜力(H Toda et al., 2014)。
  • 用于增进1-己烯环氧化性能的、硅岛(Silica island) 调节TS‐1的外部T位环境(external Ti‐site environment):探索了利用TS-1 改性催化剂改善环氧化反应中1-己烯的性能((J Yuan et al., 2023)。
  • 采用非均相半导体材料进行1-己烯的气相光催化氧化:描述了通过气相光催化氧化进行1, 2-环氧己烷的合成,重点关注了过程的选择性和效率(EA Kamba et al., 2023)。

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

59.0 °F - closed cup

flash_point_c

15 °C - closed cup

ppe

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

法规信息

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W J Choi et al.
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Ijaz Gul et al.
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Environmental science. Processes & impacts, 22(1), 66-83 (2019-11-02)
Secondary organic aerosol (SOA) particles are ubiquitous in air and understanding the mechanism by which they grow is critical for predicting their effects on visibility and climate. The uptake of three organic nitrates into semi-solid SOA particles formed by α-pinene
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Chemistry, an Asian journal, 12(17), 2271-2277 (2017-06-20)
Development of inexpensive, easily prepared, non-toxic, and efficient catalysts for the cycloaddition of CO

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