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4,4'-(1,3-Adamantanediyl)diphenol, also known as 1-Adamantanyl-4,4'-dihydroxy biphenyl, is a versatile chemical compound characterized by an adamantane core and two hydroxyl groups. It is primarily recognized for its role as a stabilizer in the production of polyvinyl chloride (PVC) plastics and other polymers, as well as for its antioxidant properties in various industrial applications.

37677-93-3

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37677-93-3 Usage

Uses

Used in Plastics and Polymer Industry:
4,4'-(1,3-Adamantanediyl)diphenol is used as a stabilizer for [application reason] to prevent degradation and deterioration of PVC plastics and other polymers caused by heat, light, and oxygen exposure. Its unique molecular structure contributes to the enhanced stability and durability of these materials.
Used in Rubber Manufacturing:
In the rubber industry, 4,4'-(1,3-Adamantanediyl)diphenol is used as an antioxidant for [application reason] to protect rubber materials from oxidative degradation, thereby extending their service life and maintaining their performance characteristics.
Used in Adhesives and Coatings Production:
4,4'-(1,3-Adamantanediyl)diphenol is utilized as an antioxidant in the manufacturing of adhesives and coatings for [application reason] to ensure the long-term integrity and performance of these products by preventing degradation due to environmental factors.
Used in Specialty Chemicals and Pharmaceutical Synthesis:
4,4'-(1,3-Adamantanediyl)diphenol serves as a valuable building block in the synthesis of specialty chemicals and pharmaceuticals for [application reason] its unique molecular structure allows for the creation of novel compounds with specific properties and applications in various fields.
Used in Materials Science and Chemical Engineering:
4,4'-(1,3-Adamantanediyl)diphenol is important in the field of materials science and chemical engineering for [application reason] its versatile molecular structure enables the development of new materials with improved properties and performance.

Check Digit Verification of cas no

The CAS Registry Mumber 37677-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,7 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37677-93:
(7*3)+(6*7)+(5*6)+(4*7)+(3*7)+(2*9)+(1*3)=163
163 % 10 = 3
So 37677-93-3 is a valid CAS Registry Number.

37677-93-3 Well-known Company Product Price

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  • Aldrich

  • (405051)  4,4′-(1,3-Adamantanediyl)diphenol  98%

  • 37677-93-3

  • 405051-250MG

  • 1,192.23CNY

  • Detail

37677-93-3SDS

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 4-[3-(4-hydroxyphenyl)-1-adamantyl]phenol

1.2 Other means of identification

Product number -
Other names 4,4'-(1,3-Adamantanediyl)bisphenol

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:37677-93-3 SDS

37677-93-3Relevant academic research and scientific papers

Polymerization kinetics of adamantane-based dicyanate ester and thermal properties of resulting polymer

Galukhin, Andrey,Islamov, Daut,Nikolaev, Ilya,Nosov, Roman,Taimova, Guzel,Vyazovkin, Sergey

, (2021)

The kinetics of liquid-state polymerization of adamantane-based dicyanate ester has been studied for the first time by means of conventional and temperature-modulated DSC. It has been detected that the later stages of polymerization undergo a transition from kinetic- to diffusion-controlled regime. Detailed analysis of the polymerization kinetics in the reaction-controlled regime has revealed that the process rate can be well described in the frameworks of the presently proposed autocatalytic quasi-one-step model. The proposed model eliminates arbitrarily guessing the value for the initial conversion that provides a reasonable alternative to the broadly used truncated Sestak-Berggren model. The adamantane-based dicyanate ester polymerization product demonstrates markedly higher thermal stability and glass transition temperature compared to those of dicyanate esters with flexible hydrocarbon bridging units. The obtained experimental results confirm our hypothesis about the influence of the rigidity of cyanate ester molecule on its reactivity and thermal properties of the corresponding polymer product.

Adamantane-based epoxy resin and siloxane-modified adamantane-based epoxy resin: Characterization of thermal, dielectric and optical properties

Tsai,Wu,Yang,Wang

, p. 11 - 18 (2015)

An adamantane-based epoxy resin (ADEP) and a siloxane-modified adamantane-based epoxy resin (Siloxane-ADEP) were synthesized, and their chemical structures were confirmed from FT-IR, 1H, 13C and 29Si NMR spectroscopy measurements. The morphological, thermal, dielectric and optical properties of ADEP and Siloxane-ADEP were studied. The introduction of the adamantane group into the chain of the epoxy resin resulted in improvements in the thermal, mechanical and dielectric properties. These results can be explained in terms of the tricyclic hydrocarbon of the adamantane in a diamond lattice structure and the movement of polymer chains being limited by chair-form cyclohexane rings, resulting in an immobile epoxy structure. Moreover, Siloxane-ADEP exhibited good thermal, mechanical and dielectric properties that were similar to those of epoxy resin, and its better processability may extend its application to electronic packing materials. The UV-Vis transmission spectra revealed that the adamantane-containing epoxy membranes exhibited novel ultraviolet light-filtering properties.

Organic compound, electronic component and electronic device

-

Paragraph 0173-0177, (2020/09/20)

The invention belongs to the technical field of organic materials, and particularly provides an organic compound which is of a structure formed by taking adamantyl as a core and connecting two nitrogen-containing heteroaryl groups to adamantane through a connecting group. The compound is suitable for being applied to an electron transport layer of an electronic component. The invention also provides an electronic component and an electronic device comprising the compound. The organic compound can improve the electron transport performance of the electronic component.

Dielectric materials

-

Paragraph 58, (2020/02/20)

The present invention relates to a novel class of polymers which can be used as dielectric material for the preparation of passivation layers in electronic devices. The polymers are prepared from polymerizable compounds having mesogenic groups and they pr

Cyanate ester compound, curable resin composition containing the same, and hardened product thereof

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Page/Page column 38-39, (2018/04/25)

The present invention is a cyanate ester compound represented by the following formula (1): wherein Ar represents an aromatic ring; R1 each independently represents a hydrogen atom, an alkyl group, or an aryl group; n each independently represe

Amine derivative containing adamantane structure and preparation method and application thereof

-

Paragraph 0028; 0029; 0030, (2016/10/07)

The invention relates to an amine derivative containing an adamantane structure and a preparation method and application thereof. The amine derivative solves the technical problem that in the prior art, a small quantity of adamantane and adamantane derivatives are applied to high polymers. The invention further discloses a molecular formula, the preparation method and application of the amine derivative. The amine derivative can meet the application requirement for electronic and composite materials and can be widely applied to aerospace, defense industry and other fields.

REACTION OF PHENOL WITH 3-METHYLENEBICYCLONONAN-7-ONE IN THE PRESENCE OF ALUMINUM DIPHENYL DITHIOPHOSPHATE

Kozlikovskii, Ya. V.,Koshchii, V. A.,Rodionov, V. N.,Yurchenko, A. G.,Olifirov, D. I.

, p. 1100 - 1103 (2007/10/02)

The reaction of phenol with 3-methylenebicyclononan-7-one in the presence of aluminum diphenyl dithiophosphate led to a mixture of the isomeric 1,3-bis(hydroxyphenyl)adamantanes, 1-hydroxyphenyl-3-hydroxyadamantanes, and 3-hydroxy-1-adamantyl phenyl ether, in which 1,3-bis(2-hydroxyphenyl)adamantane usually predominated.

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