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2,2"-Dihydroxy-4,4"-2(hydroxypropane-1,3-diyldioxy)dibenzophenone is a complex organic compound characterized by a benzophenone backbone with two hydroxy groups at the 2,2" positions and a 2(hydroxypropane-1,3-diyldioxy) bridging group at the 4,4" positions. 2,2"-Dihydroxy-4,4"-2(hydroxypropane-1,3-diyldioxy)dibenzophenone is known for its ability to absorb and convert harmful UV radiation into harmless heat, making it a valuable ingredient in various applications.

23911-85-5

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23911-85-5 Usage

Uses

Used in Sunscreen Industry:
2,2"-Dihydroxy-4,4"-2(hydroxypropane-1,3-diyldioxy)dibenzophenone is used as a UV filter in sunscreen formulations for its capability to provide protection against both UVB and UVA radiation. Its inclusion in sunscreens helps in shielding the skin from potential damage caused by the sun's harmful rays.
Used in Plastics and Adhesives Industry:
2,2"-Dihydroxy-4,4"-2(hydroxypropane-1,3-diyldioxy)dibenzophenone is also utilized in the production of certain plastics and adhesives, where its chemical properties contribute to the desired characteristics of the final products, such as durability and resistance to environmental factors.
Environmental Research:
Due to its potential for environmental persistence, ongoing research is being conducted to understand the impact of 2,2"-Dihydroxy-4,4"-2(hydroxypropane-1,3-diyldioxy)dibenzophenone on the ecosystem and human health. This research aims to evaluate and mitigate any possible adverse effects that the compound may have on the environment and living organisms.

Check Digit Verification of cas no

The CAS Registry Mumber 23911-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,1 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23911-85:
(7*2)+(6*3)+(5*9)+(4*1)+(3*1)+(2*8)+(1*5)=105
105 % 10 = 5
So 23911-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C29H24O7/c30-21(17-35-22-11-13-24(26(31)15-22)28(33)19-7-3-1-4-8-19)18-36-23-12-14-25(27(32)16-23)29(34)20-9-5-2-6-10-20/h1-16,21,30-32H,17-18H2

23911-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[3-(4-benzoyl-3-hydroxyphenoxy)-2-hydroxypropoxy]-2-hydroxyphenyl]-phenylmethanone

1.2 Other means of identification

Product number -
Other names 1,3-bis(4-benzoyl-3-hydroxyphenoxy)-2-propanol

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:23911-85-5 SDS

23911-85-5Relevant academic research and scientific papers

Macromolecular chain structure design, synthesis and analysis of poly(l-lactide) linking ultraviolet absorbing groups

Ge, Feijie,Huang, Yun,Luo, Yu,Jiang, Long,Dan, Yi

, p. 63118 - 63127 (2015/02/19)

Poly(l-lactide) (PLA) with different chain structures was designed, and successfully synthesized by ring opening polymerization using 2-hydroxy-4-(3-methacryloxy-2-hydroxylpropoxy) benzophenone (BPMA), 2,2′-dihydroxy-4,4′-(2-hydroxylpropoxy) dibenzophenone (DHDBP) and 2-hydroxy-4-(2,3-dihydroxylpropoxy) benzophenone (HPBP) as initiators, respectively, to produce corresponding PLA-B (end-capped with BPMA), PLA-DB (end-capped with DHDBP) and PLA-HB-PLA (blocked with HPBP in the middle). High-molecular-weight PLA-DB400 with good visible light transparency and UV opacity was prepared. The chemical structures of the samples were characterized, the crystallization behavior, thermal stability, UV absorption properties and transmittance of PLA were investigated and analyzed. Results of GPC and DSC reveal that when the number average molecular weights (Mn) of PLA are around 4000, termination of a UV absorbing group like DHDBP greatly restricts the crystallization of PLA due to the larger volume and rigidity of the end-capping group, but increasing Mn to about 12000 or higher weakens the hindering effect, resulting in a similar degree of crystallization (Xc). TG results show that PLA-DB400 has the best thermal stability due to the highest molar mass. When the UV absorber is blocked in the PLA chain, the restriction and steric hindrance of the absorber are much stronger than that in the end-capped material, making Xc significantly reduced. UV absorbance of the PLA solutions reveals that the introduction of UV absorbing groups gives an absorption to UV light below 350 nm and the position of the introduced groups has no influence on the UV absorption properties although the content of the UV group does enhance the UV absorbance, of which PLA-DB has the highest since DHDBP bears two 2-dihydroxybenzophenone groups. The transparency of PLA films is neither affected by position nor content of the introduced UV absorbing groups, which is very beneficial for the application of PLA in packaging materials that require high transparency.

Benzophenones containing an ester functional group and their use in polymers

-

, (2008/06/13)

The present invention relates to new hydroxybenzophenones containing an ester functional group and to the use of these compounds as UV absorbers in organic polymers. More precisely, the new hydroxybenzophenones are 1,3-di(4-benzoyl-3-hydroxyphenoxy)-2-propanol carboxylates which preferably have a molecular mass of at least 500. These benzophenones can be employed as anti-UV agents in organic polymers, either by themselves or jointly with known benzophenones of lower molecular mass, such as 2-hydroxy-4-alkoxybenzophenones.

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