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22915-73-7

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22915-73-7 Usage

Formation

Esterification of 1,6-hexanediol with benzoic acid

Common Uses

Plasticizer in lubricants, adhesives, and polymers
Enhances flexibility and durability

Antimicrobial Properties

Suitable for use in personal care products (soaps and lotions)

Toxicity

Low-toxicity alternative to other plasticizers

Versatility

Valued for its ability to enhance the performance of different materials and products

Applications

Various industries (chemical, personal care, manufacturing)

Check Digit Verification of cas no

The CAS Registry Mumber 22915-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,1 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22915-73:
(7*2)+(6*2)+(5*9)+(4*1)+(3*5)+(2*7)+(1*3)=107
107 % 10 = 7
So 22915-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H22O4/c21-19(17-11-5-3-6-12-17)23-15-9-1-2-10-16-24-20(22)18-13-7-4-8-14-18/h3-8,11-14H,1-2,9-10,15-16H2

22915-73-7SDS

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 1,6-bis-benzo[1,3]dioxol-5-yl-hexane-1,6-dione

1.2 Other means of identification

Product number -
Other names 1,6-Bis-benzo[1,3]dioxol-5-yl-hexan-1,6-dion

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:22915-73-7 SDS

22915-73-7Downstream Products

22915-73-7Relevant articles and documents

Dipole-Dipole Interactions between the Terminal Groups of l,n-Diarenecarboxy Alkanes, n=1, 2, ..., 6

Macanita, Antonio L.,Magalhaes, Jorge,Dias, Antonio,Teles, Henrique,Iglesias, Emilia

, p. 4011 - 4016 (1990)

The mutual interaction between the end groups of bichromophoric molecules is studied using absorption and fluorescence techniques (steady-state and time-resolved).With three series of di-1,n-arenecarboxyalkanes (arene = benzene, naphthalene and anthracene; n = 1,2,3,5 and 6) and a series of 1-pyrenecarboxy, n-(N-methyl, N-phenylamino) alkanes (n = 2,3,4,5,6 and 9), it is found that model compounds such as the methyl, ethyl and hexyl esters of benzene, naphthalene, anthracene and pyrene differ from the bichromophoric compounds in their absorption and emission spectra, molar absorption coefficients and radiative rate constants.These differences decrease with the mean value of the sixth power of the end-to-end distance, being attributed to dipole-dipole interactions between the end groups.The terminal group induces mixing of the lowest excited singlet state with higher energy states and increases the local polarizability of the medium.Two methods for evaluating the unquenched fluorescence lifetimes of bichromophoric compounds are discussed.

Metal-free transesterification catalyzed by tetramethylammonium methyl carbonate

Hatano, Manabu,Tabata, Yuji,Yoshida, Yurika,Toh, Kohei,Yamashita, Kenji,Ogura, Yoshihiro,Ishihara, Kazuaki

supporting information, p. 1193 - 1198 (2018/03/27)

Environmentally benign metal-free tetramethylammonium methyl carbonate is effective as a catalyst for the chemoselective, scalable, and reusable transesterification of various esters and alcohols in common organic solvents. In situ-generated highly active species, tetramethylammonium alkoxides, can greatly avoid self-decomposition at ≤110 °C, and are reusable. In particular, chelating substrates, such as amino alcohols, diols, triols, sugar derivatives, alkaloids, α-amino acid esters, etc., which deactivate conventional metal salt catalysts, can be used. A 100 gram scale biodiesel production was also demonstrated.

Odd-even effect of dopant molecules on clearing temperatures of nematic liquid-crystal phases

Kishikawa, Keiki,Haga, Yuri,Inoue, Takahiro,Watanabe, Tomohiro,Takahashi, Masahiro,Kohmoto, Shigeo

supporting information, p. 1465 - 1467 (2013/01/16)

Nematic liquid-crystal phases doped with the novel dopant compounds 1 (C6F5COO(CH)nOCOC6F5, n = 17) and 2 (C6H5-COO(CH)nOCOC6H 5, n = 17) showed an "opposite odd-even effect" on clearing temperatures. The tendency was exactly opposite to that reported for liquid-crystal dimers. A mechanism is postulated on the basis of the difference in the formation of molecular aggregations of even- and odd-number-dopant molecules in the host liquid-crystal molecules.

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