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1,1,1-TRIMETHYLOLETHANE TRIPROPIOLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

995-34-6

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995-34-6 Usage

Chemical composition

Derived from 1,1,1-trimethylolethane and propionic acid.

Common use

Crosslinking agent in the production of emulsion polymers and coatings.

Additional role

Reactive diluent.

Benefits

Improves adhesion, flexibility, and weatherability of coatings.

Other applications

Used in the production of plastics, resins, adhesives, and sealants.

Industrial applications

Widely utilized due to its versatility and effectiveness as a crosslinking agent.

Check Digit Verification of cas no

The CAS Registry Mumber 995-34-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 995-34:
(5*9)+(4*9)+(3*5)+(2*3)+(1*4)=106
106 % 10 = 6
So 995-34-6 is a valid CAS Registry Number.

995-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(hydroxymethyl)-2-methylpropane-1,3-diol,prop-2-ynoic acid

1.2 Other means of identification

Product number -
Other names 1,1,1-TRIMETHYLOLETHANE TRIPROPIOLATE

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:995-34-6 SDS

995-34-6Downstream Products

995-34-6Relevant academic research and scientific papers

Fabrication of highly uniform gel coatings by the conversion of surface-anchored metal-organic frameworks

Tsotsalas, Manuel,Liu, Jinxuan,Tettmann, Beatrix,Grosjean, Sylvain,Shahnas, Artak,Wang, Zhengbang,Azucena, Carlos,Addicoat, Matthew,Heine, Thomas,Lahann, Joerg,Overhage, Joerg,Braese, Stefan,Gliemann, Hartmut,Woell, Christof

, p. 8 - 11 (2014)

We report the fabrication of 3D, highly porous, covalently bound polymer films of homogeneous thickness. These surface-bound gels combine the advantages of metal-organic framework (MOF) materials, namely, the enormous flexibility and the large size of the maximum pore structures and, in particular, the possibility to grow them epitaxially on modified substrates, with those of covalently connected gel materials, namely, the absence of metal ions in the deposited material, a robust framework consisting of covalent bonds, and, most importantly, pronounced stability under biological conditions. The conversion of a SURMOF (surface-mounted MOF) yields a surface-grafted gel. These SURGELs can be loaded with bioactive compounds and applied as bioactive coatings and provide a drug-release platform in in vitro cell culture studies.

Hyperbranched poly(aroxycarbonyltriazole)s: Metal-free click polymerization, light refraction, aggregation-induced emission, explosive detection, and fluorescent patterning

Li, Hongkun,Wu, Haiqiang,Zhao, Engui,Li, Jie,Sun, Jing Zhi,Qin, Anjun,Tang, Ben Zhong

, p. 3907 - 3914 (2013)

The metal-free click polymerization (MFCP) of azide and alkyne has become a powerful tool for the synthesis of functional polytriazoles. Among which, the MFCP of propiolate and azide has been used to prepare functional linear poly(aroxycarbonyltriazole)s (PACTs). Their hyperbranched analogues, however, have been rarely prepared. In this paper, hyperbranched PACTs with satisfactory molecular weights and high regioregularities were synthesized in high yields by the MFCP of tripropiolates (1) and tetraphenylethene (TPE)-containing diazide (2) under the optimized reaction conditions without protection from oxygen and moisture. The resultant polymers are soluble in common organic solvents and thermally stable, with 5% loss of their weights at temperatures higher than 330°C. The polymers exhibit high refractive indices with low chromatic dispersion. Thanks to their contained TPE units, the polymers show the unique feature of aggregation-induced emission, and their aggregates can function as fluorescent sensors for the detection of explosives with the superamplification quenching effect. Furthermore, the polymers can be readily photo-cross-linked, yielding two-dimensional fluorescent patterns with high resolution.

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