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GLYCIDYL ISOBUTYL ETHER, also known as 1,2-Epoxy-3-isobutoxypropane, is a colorless, low viscosity organic compound with the chemical formula C7H14O2. It is primarily used as a solvent, reactive diluent, and plasticizer in various industrial applications. Known for its excellent long-term stability and superior properties such as moisture and chemical resistance, GLYCIDYL ISOBUTYL ETHER is a vital component in many industrial processes.

3814-55-9

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3814-55-9 Usage

Uses

Used in Adhesives Industry:
GLYCIDYL ISOBUTYL ETHER is used as a reactive diluent and plasticizer for improving the performance and stability of adhesives. Its moisture and chemical resistance contribute to the adhesives' durability and effectiveness.
Used in Sealants Industry:
GLYCIDYL ISOBUTYL ETHER is used as a component in sealants to enhance their long-term stability and resistance to moisture and chemicals. This ensures the sealants maintain their sealing properties over time.
Used in Coatings Industry:
GLYCIDYL ISOBUTYL ETHER is used as a solvent and reactive diluent in the formulation of coatings. Its properties help improve the coatings' resistance to moisture and chemicals, as well as their overall performance.
Used in Paints Industry:
GLYCIDYL ISOBUTYL ETHER is used as a solvent and reactive diluent in paint formulations. It contributes to the paint's long-term stability, moisture and chemical resistance, and overall performance.
However, it is important to note that due to its epoxy nature, GLYCIDYL ISOBUTYL ETHER can cause skin and eye irritation, and prolonged exposure may have negative health effects. Despite these potential risks, it remains a vital component in many industrial processes due to its versatile properties.

Check Digit Verification of cas no

The CAS Registry Mumber 3814-55-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,1 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3814-55:
(6*3)+(5*8)+(4*1)+(3*4)+(2*5)+(1*5)=89
89 % 10 = 9
So 3814-55-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2/c1-6(2)3-8-4-7-5-9-7/h6-7H,3-5H2,1-2H3

3814-55-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylpropoxymethyl)oxirane

1.2 Other means of identification

Product number -
Other names iso-butyl glycidyl ether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3814-55-9 SDS

3814-55-9Relevant academic research and scientific papers

Liquid-Liquid-Extraction of Metal Ions with Lariat Ethers

Gloe, K.,Muehl, P.,Beger, J.,Poeschmann, C.,Petrich, M.,Beyer, L.

, p. 413 - 421 (2007/10/02)

Lariat ethers of various ring size and substitution are synthesized and characterized by physical data and chemical analysis.The extraction behaviour of the crown compounds towards Na+, K+, Cs+ and Ag+ in a picric acid solution has been investigated.The extraction constants for 1:1 and 1:2 complexes are determined using the equilibrium distribution data.The results show that the flexible side chain in the investigated compounds has in no case a positive effect on the metal picrate extraction.

Synthesis and β-Adrenergic Blocking Activity of New Aliphatic Oxime Ethers

Leclerc, Gerard,Bieth, Nicole,Schwartz, Jean

, p. 620 - 624 (2007/10/02)

New β-adrenergic blocking agents, most of which do not contain an aromatic nucleus, were synthesized.They were derived either from alkylamino-aliphatic oxime ethers, or alkylamino-aliphatic ethers.Most active among these are O-acetoxime (8; trachea pA2=7.65) and 1-isobutoxy-3-(tert-butylamino)-2-propanol (15, trachea pA2=7.49), both of which displayed bronchoselectivity (β2/β1 ratio ca. 15).The role and importance of the aromatic nucleus in this class of compounds are discussed

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