5047-02-9

Usage

Uses

Used in Plastics and Rubber Industry:
Dinonyldimethanol is used as a plasticizer to enhance the flexibility, durability, and impact resistance of various plastics and rubbers. Its ability to improve these properties makes it a valuable additive in the production of PVC and polyurethane products.
Used in Polymer and Resin Production:
In the polymer and resin industry, dinonyldimethanol is utilized as a plasticizer to increase the workability and processability of materials. Its high boiling point and low volatility contribute to the thermal stability of the final products, which is crucial for various applications.
However, it is important to note that dinonyldimethanol has been subject to controversy due to its potential toxicity and environmental impact. As a result, its use is regulated and restricted in certain regions to minimize any adverse effects on human health and the environment.

Upstream product

• 863305-32-2 diphenic acid 
• 20246-81-5 4,4'-dinitrodiphenic acid 
• 23305-76-2 dimethyl 4,4’-dinitro-2,2’-biphenyldicarboxylate 

Downstream Products

• 1429526-40-8 4-{(1E)-3-[(2’-{[(3E)-4-(4-{[4-(3-nitrilepropoxy)benzoyl]oxy}phenyl)-2-oxobut-3-enyl]oxy}-4,4’-dinitro-1,1-biphenyl-2-yl)methoxy]-3-oxoprop-1-enyl}phenyl 4-(3-nitrilepropoxy)benzoate 
• 1345477-12-4 [4,4'-dinitro-2'-({[(2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenyl]methoxy}phenyl)prop-2-enoyl]oxy}methyl)-1,1'-biphenyl-2-yl]methyl (2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenyl]methoxy}phenyl)prop-2-enoate 
• 1345477-13-5 [4,4'-diamino-2'-({[(2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenyl]methoxy}phenyl)prop-2-enoyl]oxy}methyl)-1,1'-biphenyl-2-yl]methyl (2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenyl]methoxy}phenyl)prop-2-enoate 
• 1345478-75-2 [4,4'-dinitro-2'-({[(2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)-phenoxy]methyl}phenyl)prop-2-enoyl]oxy}methyl)-1,1'-biphenyl-2-yl]methyl (2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}phenyl)prop-2-enoate 
• 1345478-77-4 [4,4'-diamino-2'-({[(2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}phenyl)prop-2-enoyl]oxy}methyl)-1,1'-biphenyl-2-yl]methyl (2E)-3-(4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}phenyl)prop-2-enoate 

Relevant academic research and scientific papers

Macrolactones and crown ethers derived from biphenyl. Electronic and steric influence of substituents on its complexation ability

Electronic effects as well as steric hindrance must be considered in order to compare the ability of macrolactones and crown ethers for complexing alkali cations and Hg(SCN)2.

Absolute Configuration Assignment from Optical Rotation Data by Means of Biphenyl Chiroptical Probes

A non-empirical approach for the assignment of the absolute configuration of chiral 2-alkyl-substituted carboxylic acids and primary amines by [α]D measurements has been developed. The method requires the conversion of the chiral acids or amines into the corresponding 4,4′-disubstituted biphenylamides or biphenylazepines, respectively. In these derivatives a central-to-axial chirality transfer induces a preferred torsion in the biphenyl moiety revealed by the sign of the biphenyl A band in the ECD spectrum. By 4,4′-substitution on the biphenyl moiety a redshift of the A band is obtained, leading to an increase of its relative contribution to optical rotation. This allows to reliably establish a direct correlation between the [α]D sign, the biphenyl twist and, then, the substrate absolute configuration. This approach thus constitutes a really practical and reliable method to assign the absolute configuration of chiral carboxylic acids and primary amines by simple and straightforward [α]D measurement, readily obtainable by a routine instrumentation like the polarimeter.

PHOTOALIGNING MATERIAL

The present invention relates to a copolymer for the photoalignment of liquid crystals comprising a photoreactive group as given below in formula (I), compositions thereof, and its use for optical and electro optical devices, especially liquid crystal dev

PHOTOALIGNING MATERIALS

The present invention relates to polymer, homo- or copolymer or oligomer for the photoalignment of liquid crystals, especially for the planar orientation of liquid crystals, comprising a main chain and a side chain, wherein the side chain and/or main chain comprises a polar group, compositions thereof, and its use for optical and electro optical devices, especially liquid crystal devices (LCDs).

PHOTOALIGNING MATERIALS

The present invention relates to polymer, homo- or copolymer or oligomer, which, when irradiated with polarised light orients perpendicular to the polarization direction of polarized actinic light, for the photoalignment of liquid crystals, especially for the planar orientation of liquid crystals, and which derives from at least one monomer (I), compositions thereof, and its use for optical and electro optical devices, such as, liquid crystal devices (LCDs), especially for planar orientation of liquid crystals.

PHOTOCROSSLINKABLE MATERIALS COMPRISING ALICYCLIC GROUP

A diamine compound of formula (I) is proposed as well as polymers, copolymers, polyamic acids, polyamic acid esters, or polyimides based on such compound.