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3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is a polyol compound with the chemical formula C11H20O6, featuring multiple epoxide functional groups. It is commonly utilized as a crosslinking or curing agent in the production of epoxy resins, which are widely used in adhesives, coatings, and composite materials.

13236-00-5

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13236-00-5 Usage

Uses

Used in Adhesives Industry:
3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is used as a crosslinking agent for enhancing the strength, durability, and chemical resistance of adhesives.
Used in Coatings Industry:
3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is used as a curing agent to improve the performance and properties of coatings, making them more resistant to wear and environmental factors.
Used in Composite Materials Industry:
3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is used as a crosslinking agent to increase the strength and durability of composite materials, which are essential in various applications such as automotive, aerospace, and construction.
Used in Polyurethane Foams Production:
3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is used as a key component in the manufacture of polyurethane foams, contributing to their structural integrity and performance characteristics.
Used in Pharmaceutical Industry:
3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is used in the development of certain pharmaceutical products, potentially offering benefits in drug formulation and delivery.
Used in Cosmetic Products:
3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is utilized in the formulation of cosmetic products, where it may contribute to the product's efficacy, texture, and stability.

Check Digit Verification of cas no

The CAS Registry Mumber 13236-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,3 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13236-00:
(7*1)+(6*3)+(5*2)+(4*3)+(3*6)+(2*0)+(1*0)=65
65 % 10 = 5
So 13236-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H24O7/c15-7-14(8-16-1-11-4-19-11,9-17-2-12-5-20-12)10-18-3-13-6-21-13/h11-13,15H,1-10H2

13236-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(oxiran-2-ylmethoxy)-2,2-bis(oxiran-2-ylmethoxymethyl)propan-1-ol

1.2 Other means of identification

Product number -
Other names EINECS 236-210-6

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:13236-00-5 SDS

13236-00-5Downstream Products

13236-00-5Relevant academic research and scientific papers

Synthesis of new pentaerythritol-based gemini surfactants

Murguía,Grau

, p. 1229 - 1232 (2001)

New dimeric or gemini surfactants bearing double-chain with two or four sulfonate groups, and quadruple-chain with four sulfonate groups, were prepared from pentaerythritol in good overall yields. All these surfactants showed excellent surface-active prop

PEHAM DENDRIMERS FOR USE IN AGRICULTURE

-

Page/Page column 35-36, (2011/05/11)

Specific PEHAM dendrimers are used in a formulation with an active agent for agricultural purposes, particularly for increasing the efficacy of the active agent in various ways, such as by improving solubility of the active agent in the formulation, by improving adhesion and penetration of the active agent to plant surfaces, by improving the water- fastness of the active agent to the plant or seed, by providing protection of the active agent from UV damage, by increasing soil penetration of the active agent to reach the plant roots or under soil parts, or by reducing soil adhesion of the active agent to reach the plant roots or under soil parts, or reducing enzymatic degradation of the active agent by the plant or seed or microorganisms in the soil.

DENDRITIC POLYMERS WITH ENHANCED AMPLIFICATION AND INTERIOR FUNCTIONALITY

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Page/Page column 73-74, (2010/11/24)

Dendritic polymers with enhanced amplification and interior functionality are disclosed. These dendritic polymers are made by use of fast, reactive ring-opening chemistry (or other fast reactions) combined with the use of branch cell reagents in a controlled way to rapidly and precisely build dendritic structures, generation by generation, with cleaner chemistry, often single products, lower excesses of reagents, lower levels of dilution, higher capacity method, more easily scaled to commercial dimensions, new ranges of materials, and lower cost. The dendritic compositions prepared have novel internal functionality, greater stability (e.g., thermal stability and less or no reverse Michael's reaction), and reach encapsulation surface densities at lower generations. Unexpectedly, these reactions of polyfunctional branch cell reagents with polyfunctional cores do not create cross-linked materials. Such dendritic polymers are useful as demulsifiers for oil/water emulsions, wet strength agents in the manufacture of paper, proton scavengers, polymers, nanoscale monomers, calibration standards for electron microscopy, making size selective membranes, and agents for modifying viscosity in aqueous formulations such as paint. When these dendritic polymers have a carried material associated with their surface and/or interior, then these dendritic polymers have additional properties for carrying materials due to the unique characteristics of the dendritic polymer, such as for drug delivery, transfection, and diagnostics.

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