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Key Documents

251747

Sigma-Aldrich

辛基缩水甘油醚

98%

同義詞:

2-乙基己基缩水甘油醚, 3-环氧丙烷

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About This Item

經驗公式(希爾表示法):
C11H22O2
CAS號碼:
分子量::
186.29
EC號碼:
MDL號碼:
分類程式碼代碼:
12162002
PubChem物質ID:
NACRES:
NA.23

品質等級

化驗

98%

形狀

liquid

折射率

n20/D 1.434 (lit.)

bp

60-62 °C/0.3 mmHg (lit.)

密度

0.891 g/mL at 25 °C (lit.)

SMILES 字串

CCCCC(CC)COCC1CO1

InChI

1S/C11H22O2/c1-3-5-6-10(4-2)7-12-8-11-9-13-11/h10-11H,3-9H2,1-2H3

InChI 密鑰

BBBUAWSVILPJLL-UHFFFAOYSA-N

應用

  • Solution properties of N-(2-allyl-butyl ether)-O-carboxymethyl chitosan and N-(2-allyl-isooctyl ether)-O-carboxymethyl chitosan.: This study explores the solution properties and potential applications of modified chitosan derivatives. It highlights their use in creating biocompatible coatings and medical device adhesives due to their enhanced solubility and functional properties (Liu et al., 2021).
  • All-Polycarbonate Thermoplastic Elastomers Based on Triblock Copolymers Derived from Triethylborane-Mediated Sequential Copolymerization of CO(2) with Various Epoxides.: This research details the development of thermoplastic elastomers using 2-Ethylhexyl glycidyl ether as a monomer. These materials show promise in life science manufacturing for creating advanced epoxy systems and low viscosity epoxy resin modifiers (Jia et al., 2020).
  • O-Carboxymethyl chitosan-based pH-responsive amphiphilic chitosan derivatives: Characterization, aggregation behavior, and application.: This paper discusses the creation of pH-responsive chitosan derivatives for use in biocompatible coatings and medical device adhesives. The modifications with 2-Ethylhexyl glycidyl ether improve their functionality and application potential in the medical field (Liu et al., 2020).

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Skin Irrit. 2 - Skin Sens. 1

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 2

閃點(°F)

206.6 °F - closed cup

閃點(°C)

97 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


分析證明 (COA)

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CO2 cycloaddition with epoxides at low temperature and pressure has been broadly recognized as an ambitious but challenging goal, which requires the catalysts to have precisely controlled Lewis acid sites. Here, we demonstrate that both stereochemical environment and oxidation state

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