Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane is a chemical compound characterized by its molecular formula C18H32O3. It is a clear, colorless liquid with a molecular weight of 296.44 g/mol. 1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane is highly reactive due to the presence of allyl groups, which makes it suitable for a variety of industrial applications. However, it is important to handle 1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane with care, as it may cause irritation to the skin, eyes, and respiratory tract.

682-08-6

Post Buying Request

682-08-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

682-08-6 Usage

Uses

Used in Polymer and Resin Production:
1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane is used as a crosslinking agent in the production of polymers and resins. Its high reactivity allows it to effectively bind and stabilize the polymer chains, resulting in improved mechanical properties and durability of the final product.
Used in Organic Synthesis:
1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane is also used in the synthesis of other organic compounds. Its reactive allyl groups can be utilized in various chemical reactions, enabling the creation of a wide range of products with diverse applications across different industries.
Used in Coatings Industry:
In the coatings industry, 1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane is used as a crosslinking agent for the production of high-performance coatings. Its ability to form strong chemical bonds with other components in the coating formulation enhances the adhesion, hardness, and resistance to environmental factors such as UV radiation, moisture, and chemicals.
Used in Adhesives Industry:
1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane is used as a crosslinking agent in the formulation of adhesives. Its reactivity helps to create strong bonds between the adhesive and the substrate, resulting in improved bonding strength and durability.
Used in Composite Materials:
In the composite materials industry, 1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane is used as a crosslinking agent to improve the mechanical properties and thermal stability of the composites. Its ability to form covalent bonds with the matrix and reinforcing fibers enhances the overall performance of the composite materials, making them suitable for various high-demand applications.
Overall, 1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane is a versatile chemical compound with a wide range of applications in various industries, primarily due to its high reactivity and ability to act as a crosslinking agent. However, it is crucial to handle 1-(allyloxy)-2,2-bis[(allyloxy)methyl]butane with caution to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 682-08-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 682-08:
(5*6)+(4*8)+(3*2)+(2*0)+(1*8)=76
76 % 10 = 6
So 682-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O3/c1-5-9-16-12-15(8-4,13-17-10-6-2)14-18-11-7-3/h5-7H,1-3,8-14H2,4H3

682-08-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-prop-2-enoxy-2,2-bis(prop-2-enoxymethyl)butane

1.2 Other means of identification

Product number -
Other names trimethylolpropane allyl 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:682-08-6 SDS

682-08-6Relevant articles and documents

Thermomechanical Formation-Structure-Property Relationships in Photopolymerized Copper-Catalyzed Azide-Alkyne (CuAAC) Networks

Baranek, Austin,Song, Han Byul,McBride, Mathew,Finnegan, Patricia,Bowman, Christopher N.

, p. 1191 - 1200 (2016/03/25)

Bulk photopolymerization of a library of synthesized multifunctional azides and alkynes was carried out toward developing structure-property relationships for CuAAC-based polymer networks. Multifunctional azides and alkynes were formulated with a copper catalyst and a photoinitiator, cured, and analyzed for their mechanical properties. Material properties such as the glass transition temperatures (Tg) show a strong dependence on monomer structure with Tg values ranging from 41 to 90 °C for the series of CuAAC monomers synthesized in this study. Compared to the triazoles, analogous thioether-based polymer networks exhibit a 45-49 °C lower Tg whereas analogous monomers composed of ethers in place of carbamates exhibit a 40 °C lower Tg. Here, the formation of the triazole moiety during the polymerization represents a critical component in dictating the material properties of the ultimate polymer network where material properties such as the rubbery modulus, cross-link density, and Tg all exhibit strong dependence on polymerization conversion, monomer composition, and structure postgelation.

BIO-NANO POWER CELLS AND THEIR USES

-

Paragraph 0508; 0509; 0510; 0511, (2014/01/08)

The present invention concerns bio-nano power cells and methods of their manufacture and use. More particularly, the present invention relates to the preparation of bio-nano power cells that are biocompatible and capable of producing flash, intermittent, or continuous power by electrolyzing compounds in biological systems.

Dendritic nanospace constructed by only glycerol units enhanced uptake of a fluorescent molecule in aqueous solution

Lee, Haejoo,Ooya, Tooru

supporting information; experimental part, p. 546 - 548 (2012/02/05)

A polyglycerol dendrimer (PGD) of generation 2, which consists of only glycerol units, constructed nanospace capable of uptake of a fluorescent molecule with a 1:1 stoichiometry. On the other hand, a PGD of generation 1 trapped the molecule at the outer part.

Liquid epoxy compound and process for preparing the same

-

, (2008/06/13)

A liquid trifunctional epoxy compound with a total chlorine content of 100 ppm or less represented by general formula (1) is obtained by epoxidizing a triallyl ether represented by general formula (2) with a peroxide and the liquid epoxy compound is useful as a diluent in a variety of applications, particularly useful as a liquid encapsulating material in electronic applications: R[—(OCH2CH2)n—OG]3??(1) R[—(OCH2CH2)n—O—CH2—CH═CH2]3??(2) (wherein R is a trivalent hydrocarbon group in which 3 different carbon atoms participate in bond formation or, more particularly, a straight-chain or branched hydrocarbon group containing 3-10 carbon atoms, a cycloalkane group containing 6 carbon atoms or a hydrocarbon group containing 7-20 carbon atoms and consisting of hydrocarbon chains and cycloalkane rings, n is 0, 1, or 2 and G is glycidyl group).

Alkylation of Pentaerythritol and Trimethylolpropane, Two Very Hydrophilic Polyols, by Phase-Transfer Catalysis.

Nouguier, R. M.,Mchich, M.

, p. 3296 - 3298 (2007/10/02)

Two very hydrophilic polyols, pentaerythritol and trimethylolpropane , can be etherified in good yields by phase-transfer catalysis with allyl chloride or heptyl bromide as alkylating agents.Ion pairs solubilities, lipophilicities of catalysts, and nature of the reaction products which are key factors in achievement of this PTC reaction are discussed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 682-08-6