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2655-95-0

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2655-95-0 Usage

Chemical Family

Alkylbenzenes

Physical State

Colorless to light yellow liquid

Odor

Faint aromatic

Solubility

Insoluble in water, soluble in most organic solvents

Primary Uses

a. Plasticizer in polymers, resins, and industrial applications
b. Lubricant additive in paints, adhesives, and coatings
c. Raw material for surfactants, detergents, and industrial chemicals

Inhalation

Irritation to the respiratory system

Ingestion

Potential health risks

Skin Absorption

Irritation and potential health risks

Safety Precautions

Proper handling and safety measures necessary to minimize exposure and health risks

Check Digit Verification of cas no

The CAS Registry Mumber 2655-95-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2655-95:
(6*2)+(5*6)+(4*5)+(3*5)+(2*9)+(1*5)=100
100 % 10 = 0
So 2655-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C26H46/c1-3-5-7-9-11-13-15-17-19-25-21-23-26(24-22-25)20-18-16-14-12-10-8-6-4-2/h21-24H,3-20H2,1-2H3

2655-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-didecylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,p-didecyl

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:2655-95-0 SDS

2655-95-0Relevant articles and documents

Poly(benzodithiophenes)

-

, (2008/06/13)

The invention relates to novel poly(benzodithiophenes), their use as semiconductors or charge transport materials, in optical, electro-optical or electronic devices like for example liquid crystal displays, optical films, organic field effect transistors (FET or OFET) for thin film transistor liquid crystal displays and integrated circuit devices such as RFID tags, electroluminescent devices in flat panel displays, and in photovoltaic and sensor devices, and to a field effect transistor, light emitting device or ID tag comprising the novel polymers.

Synthesis and unusual physical behavior of a photorefractive polymer containing tris(bipyridyl)ruthenium(II) complexes as a photosensitizer and exhibiting a low glass-transition temperature

Wang, Qing,Wang, Liming,Yu, Luping

, p. 12860 - 12868 (2007/10/03)

This paper reports the synthesis and characterization of a low-T(g) photorefractive (PR) polymer which contains ionic ruthenium complexes as the photogenerator of charge carriers. It was expected that a combination of the highly efficient photocharge gene

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