Welcome to LookChem.com Sign In|Join Free
  • or
1,3-Propanedione, 1,3-bis[4-(1-methylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63250-26-0

Post Buying Request

63250-26-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

63250-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63250-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,5 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63250-26:
(7*6)+(6*3)+(5*2)+(4*5)+(3*0)+(2*2)+(1*6)=100
100 % 10 = 0
So 63250-26-0 is a valid CAS Registry Number.

63250-26-0SDS

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 1,3-bis(4-propan-2-ylphenyl)propane-1,3-dione

1.2 Other means of identification

Product number -
Other names 4,4'-Diisopropyl-dibenzoylmethan

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:63250-26-0 SDS

63250-26-0Relevant academic research and scientific papers

White light emission from a single component system: Remarkable concentration effects on the fluorescence of 1,3-diaroylmethanatoboron difluoride

Sakai, Atsushi,Tanaka, Mirai,Ohta, Eisuke,Yoshimoto, Yuichi,Mizuno, Kazuhiko,Ikeda, Hiroshi

supporting information; experimental part, p. 4138 - 4141 (2012/08/28)

Concentration effects on the fluorescence (FL) emission of 1,3-dibenzoylmethanatoboron difluoride (1aBF2) and its diisopropyl derivative (1bBF2) in KBr and CH2Cl2 were investigated. Powder samples of 1aBF2 and 1bBF2 in KBr exhibit yellow and white FL emissions, respectively, whose intensities and wavelengths are not significantly affected by concentration. In contrast, remarkable concentration effects on FL properties of these compounds in CH 2Cl2 solutions were observed. Increases in the concentrations of 1aBF2 and 1bBF2 from 1 × 10 -7 to ca. 2 × 10-1 M lead to dramatic changes in the FL colors from blue (398 and 411 nm, respectively) to yellow (548 and 558 nm) via white. Careful analysis of the FL spectra, involving lifetime determinations and wave deconvolutions, reveals that emissions from 1BF2 involve two FL domains, corresponding to an excited monomer and an excimer, and that concentration increases promote a continuous change from the former to the latter major FL domain. Thus, white FL of 1aBF2 and 1bBF2 is achieved by modulation of the dual FL of the excited monomer (blue) and excimer (yellow). These findings indicate that 1,3-diaroylmethanatoboron difluoride (1BF2) represents a new white emitting material that has advantageous features which arise from the fact that it is an easily prepared, low molecular weight, single component system not containing a heavy metal atom.

Photoprotective compositions comprising photosensitive 1,3,5-triazine compounds, dibenzoylmethane compounds and siliceous s-triazines substituted with two aminobenzoate or aminobenzamide groups

-

, (2010/02/16)

UV-photoprotective, topically applicable cosmetic/dermatological compositions contain: (a) at least one dibenzoylmethane compound,(b) at least one 1,3,5-triazine compound that is photosensitive in the presence of a dibenzoylmethane compound, and(c) at least one siliceous s-triazine compound substituted with two aminobenzoate or aminobenzamide groups, or a tautomeric form thereof, the 1,3,5-triazine compounds being improvedly photostable in such compositions.

PARTICULATE UV PROTECTION AGENT

-

, (2010/03/02)

The present invention relates to particulate UV protection agents which are obtainable by hydrothermal treatment of a particulate metal oxide and subsequent application of a manganese oxide coating, and to the preparation and use thereof. The present invention furthermore relates to novel compositions, in particular for topical application, which are intended, in particular, for light protection of the skin and/or hair against UV radiation and free-radical-induced stress, and to the use thereof in the above-mentioned cosmetic application.

Cosmetic/sunscreen compositions containing dibenzoylmethane compounds and dithiolane compound photostabilizers therefor

-

, (2010/04/30)

Cosmetic/sunscreen compositions contain a combination of at least one dibenzoylmethane sunscreen compound and a photostabilizing amount of at least one dithiolane compound of formula (I) below:

Photostable cosmetic compositions comprising dibenzoylmethane/pyrrolidinone compounds

-

, (2009/12/05)

Photostable UV-photoprotecting cosmetic sunscreen compositions contain (a) an effective UV-photoprotecting amount of at least one dibenzoylmethane compound sunscreen, (b) an effective radiation-photostablizing amount of at least one pyrrolidinone compound having the formula (I) below: and, advantageously, at least one liquid fatty phase and at least one lipophilic active sunscreen agent of low solubility, formulated into (c) a cosmetically acceptable support therefor.

Photoprotective cosmetic compositions comprising photostabilized dibenzoylmethane compounds and siloxane-containing arylalkyl benzoate amide compounds

-

, (2009/01/24)

Photostable, topically applicable cosmetic/dermatological compositions contain at least one dibenzoylmethane sunscreen compound and at least one photostabilizing siloxane-containing arylalkyl amide compound of formula (I) below:

Photostable UV-screening compositions comprising dibenzoylmethane/diarylbutadiene compounds

-

, (2008/06/13)

Topically applicable, photostable cosmetic/dermatological UV-screening compositions comprise (a) at least one photolabile UV-screening dibenzoylmethane compound and (b) a dibenzoylmethane photostabilizing amount of at least one 4,4-diarylbutadiene compound, formulated into a topically applicable, cosmetically/dermatologically acceptable support therefor; the weight ratio of the 4,4-diarylbutadiene compound(s) to the diarylbutadiene compound(s) is characteristically greater than 2.5 and the subject compositions are advantageously devoid of any cinnamate sunscreen.

Photoprotective UV-screening compositions comprising triazine/dibenzoylmethane/diarylbutadiene compounds

-

, (2008/06/13)

Topically applicable, photostable cosmetic/dermatological UV-screening compositions suited for photoprotecting the skin and the hair, comprise (a) at least one UV-screening dibenzoylmethane compound, (b) at least one UV-screening 1,3,5-triazine compound that is photosensitive in the presence of a dibenzoylmethane compound, and (c) a 1,3,5-triazine photostabilizing amount of at least one 4,4-diarylbutadiene compound, formulated into a topically applicable, cosmetically/dermatologically acceptable support therefor; the weight ratio of the 4,4-diarylbutadiene compound(s) to the dibenzoylmethane compound(s) is characteristically greater than 2.5 and the subject compositions are advantageously devoid of any cinnamate sunscreen.

Photostable photoprotective UV-screening compositions comprising dibenzoylmethane/methyl-benzylidenecamphor/diarylbutadiene compounds

-

, (2008/06/13)

Topically applicable, photostable cosmetic/dermatological UV-screening compositions comprise (a) at least one UV-screening dibenzoylmethane compound, (b) p-methylbenzylidenecamphor, and (c) a methylbenzylidenecamphor photostabilizing amount of at least one 4,4-diarylbutadiene compound, formulated into a topically applicable, cosmetically/dermatologically acceptable support therefor; the weight ratio of the 4,4-diarylbutadiene compound(s) to the dibenzoylmethane compound(s) is characteristically greater than 2.5 and the subject compositions are advantageously devoid of any cinnamate sunscreen.

Photostabilized dibenzoylmethane sunscreens immobilized within sol/gel matrices

-

, (2008/06/13)

Photoprotective cosmetic/dermatological compositions well suited for the UV-photoprotection of the skin, hair, nails, eyebrows, eyelashes and/or lips, contain an effective photostable and UV-photoprotecting amount of at least one dibenzoylmethane organic sunscreen immobilized within a matrix prepared via sol-gel process from at least one silicon alkoxide, at least one non-ionic surfactant and water, but in the absence of any organic solvent, formulated into a topically applicable, cosmetically/dermatologically acceptable medium therefor.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 63250-26-0