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1,3-Benzenedicarboxylic acid, 5-[(12-bromododecyl)oxy]-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184649-99-8

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184649-99-8 Usage

Molecular structure

A benzene ring with two carboxylic acid groups at positions 1 and 3, a 12-bromododecyloxy chain attached to the 5 position, and two methyl ester groups

Physical state

Clear and colorless liquid

Odor

Faintly sweet

Solubility

Soluble in organic solvents

Uses

Production of polyethylene terephthalate (PET) resin for plastic bottles and containers

Toxicity

Low-toxicity chemical

Skin and eye irritation

Low potential

Inhalation effects

May cause respiratory tract irritation

Long-term exposure effects

Adverse effects on liver and kidneys

Environmental considerations

Should be handled and used with caution to prevent harm to human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 184649-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,6,4 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 184649-99:
(8*1)+(7*8)+(6*4)+(5*6)+(4*4)+(3*9)+(2*9)+(1*9)=188
188 % 10 = 8
So 184649-99-8 is a valid CAS Registry Number.

184649-99-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(12-Bromo-dodecyloxy)-isophthalic acid dimethyl ester

1.2 Other means of identification

Product number -
Other names -

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:184649-99-8 SDS

184649-99-8Downstream Products

184649-99-8Relevant academic research and scientific papers

Solvent codeposition and cis-trans isomerization of isophthalic acid derivatives studied by STM

Vanoppen,Grim,Ruecker,De Feyter,Moessner,Valiyaveettil,Muellen,De Schryver

, p. 19636 - 19641 (1996)

Scanning tunneling microscopy (STM) was used to study physisorbed monolayers of 5-octadecyloxyisophthalic acid (C18ISA) and 5-[ω-(4′-dodecyloxy-4-azobenzeneoxy)dodecyloxy]isophthalic acid (C12(AZO)C12ISA) at a liquid/graphite interface. The acquired STM images exhibit the molecular packing of the monolayers with submolecular resolution. Monolayers formed by codeposition of solvent molecules and C18ISA or C12(AZO)C12-ISA molecules are found when 1-octanol and 1-undecanol are used as a solvent. The cis and trans isomers of C12(AZO)C12ISA, the reagent and reaction product of a reversible photoinduced reaction, are simultaneously present and are both structurally identified at the liquid/graphite interface.

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