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13236-00-5

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13236-00-5 Usage

General Description

3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is a chemical compound with the formula C11H20O6. It is a polyol compound containing multiple epoxide functional groups. 3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol is often used as a crosslinking agent or curing agent in the production of epoxy resins, which are commonly used in adhesives, coatings, and composite materials. It serves to increase the strength, durability, and chemical resistance of these materials. Additionally, it can also be used in the manufacture of polyurethane foams, as well as in certain pharmaceutical and cosmetic products. Overall, 3-(oxiranylmethoxy)-2,2-bis[(oxiranylmethoxy)methyl]propanol plays a crucial role in the production of various industrial, commercial, and consumer goods.

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 articles and documents

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

DENDRITIC POLYMERS WITH ENHANCED AMPLIFICATION AND INTERIOR FUNCTIONALITY

-

Page/Page column 77-78, (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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