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3230-09-9

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3230-09-9 Usage

General Description

1,4-di(dodecyloxy)benzene, also known as DDB, is a synthetic chemical compound often used as a surfactant or co-surfactant in various industrial and household products. It is a type of alkylaryloxybenzene sulfonate and has a long hydrophobic tail of dodecyl groups attached to a benzene ring. DDB is commonly utilized in the production of detergents, dishwashing liquids, and other cleaning products due to its excellent surfactant properties, such as its ability to reduce surface tension and increase the solubility of non-polar substances in water. However, there is growing concern over the environmental and health impacts of DDB, as it is considered a persistent organic pollutant and possible endocrine disruptor. Efforts are being made to find alternative, more eco-friendly surfactants to replace DDB in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3230-09-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,3 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3230-09:
(6*3)+(5*2)+(4*3)+(3*0)+(2*0)+(1*9)=49
49 % 10 = 9
So 3230-09-9 is a valid CAS Registry Number.

3230-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-didodecoxybenzene

1.2 Other means of identification

Product number -
Other names Hydroquinone didodecyl ether

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:3230-09-9 SDS

3230-09-9Relevant articles and documents

Synthesis of copillar[5]arene by co-oligomerization of different monomers and its application to supramolecular polymer gel

Li, Hui,Zhu, Yuanrong,Shi, Bingbing,Wu, Guiyuan,Zhang, Youming,Lin, Qi,Yao, Hong,Wei, Taibao

, p. 373 - 378 (2015)

A copillar[5]arene derivative with different repeating units was synthesized by co-oligomerization of different alkyl ethers. Copillar[5]arene-based supramolecular polymer gel was formed by a self-inclusion complexing in acetonitrile. The supramolecular polymer gel was driven by the C-H· π interactions, and presented two phases as time went on, and finally, constructed the supramolecular organic framework. Notably, the supramolecular polymer gel showed reversible gel-sol phase transitions upon heating and cooling. Meanwhile, the transparent films formed by the supramloecular gel show the potential application in the field of anti-acid rain materials.

Copolymers for iodide detection and methods thereof

-

Page/Page column 6; 26, (2020/02/03)

Copolymers having thiophene based and vinylene based moieties. Methods of producing the copolymers, and methods of utilizing the copolymers as chromogenic sensors for selective detection of iodide anion are also provided.

Supramolecular enantiomeric and structural differentiation of amino acid derivatives with achiral pillar[5]arene homologs

Ji, Jiecheng,Li, Yizhou,Xiao, Chao,Cheng, Guo,Luo, Kui,Gong, Qiyong,Zhou, Dayang,Chruma, Jason J.,Wu, Wanhua,Yang, Cheng

supporting information, p. 161 - 164 (2019/12/30)

Complexation of achiral pillar[5]arenes with chiral amines induced strong circular dichroism (CD) signals. The CD responses differed drastically depending on the nature of the amino acid guest, and they significantly varied and part of them even inverted, upon increasing the length of the alkyl chains of the pillar[5]arenes guests. Accordingly, this tactic allowed for the unprecedented simultaneous enantiomeric and structural differentiation of α-amino esters with homologous molecular hosts.

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