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133310-72-2

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133310-72-2 Usage

Type of compound

Perfluorinated chemical compound

Definition

A compound in which all hydrogen atoms have been replaced with fluorine atoms

Chemical resistance

Highly resistant to chemical and environmental degradation

Industrial applications

Commonly used as a surfactant and lubricant

Specific uses

Production of non-stick coatings, oil and water repellent fabrics, and firefighting foams

Properties

Provides a high level of chemical and thermal stability in a wide range of applications

Environmental concerns

Persistent nature and potential environmental and health risks

Release into the environment

Growing concern about the use and release of 1-(PERFLUORO-N-OCTYL)TETRADECANE into the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 133310-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,3,1 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133310-72:
(8*1)+(7*3)+(6*3)+(5*3)+(4*1)+(3*0)+(2*7)+(1*2)=82
82 % 10 = 2
So 133310-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H29F17/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(23,24)16(25,26)17(27,28)18(29,30)19(31,32)20(33,34)21(35,36)22(37,38)39/h2-14H2,1H3

133310-72-2SDS

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 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluorodocosane

1.2 Other means of identification

Product number -
Other names PC6857

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:133310-72-2 SDS

133310-72-2Downstream Products

133310-72-2Relevant articles and documents

Branching of the perfluorinated chain influences the liquid-crystalline properties of semifluorinated alkanes: Perfluorooctyl- and perfluoroisononyl-n- alkanes-a comparative study

Broniatowski,Dynarowicz-Latka,Witko

, p. 63 - 74 (2006)

Two series of semifluorinated-n-alkanes (SFAs) of comparable perfluorinated chain length but different terminal group constitution, namely perfluorooctyl-n-alkanes [F-(CF2)8-(CH2) n-H, in short F8Hn] and perfluoroisononyl-n-alkanes [(CF 3)2CF(CF2)6-(CH2) n-H, in short iF9Hn] were synthesized. Their thermal properties were analyzed by means of differential scanning calorimetry (DSC), on both heating and cooling of the samples. The textures of the synthesized semifluorinated alkanes were investigated with the microscopy in polarized light. Similar to previously investigated perfluorodecyl-n-alkanes, perfluorooctyl-n-alkanes containing fewer than 12 methylene groups form smectic B phase. F8H8, F8H9, and F8H10 show a tendency to supercool and preserve smectic B ordering even below the transition temperature. For F8H11, the phase transition from smectic B to 3D crystal structure, manifesting itself as a rapid recrystallization, has been observed. Perfluorooctyl-n-alkanes of 12 or more methylene groups do not form liquid-crystalline phases. In contrast to perfluorooctyl-n-alkanes, perfluoroisononyl-n-alkanes are not capable of liquid-crystalline phase formation, regardless of the hydrogenated moiety length and the experimental conditions.

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