14165-64-1 Usage
Chemical Structure
Benzene derivative with two hydroxyl (OH) groups and a nonyl side chain
Explanation
The compound is derived from benzene, which is a six-carbon ring with alternating single and double bonds. It has two hydroxyl groups attached to the 1st and 3rd carbon atoms and a nonyl (C9H19) side chain attached to the 5th carbon atom.
Explanation
The hydroxyl groups are polar and can form hydrogen bonds, while the nonyl side chain is a long, nonpolar hydrocarbon chain.
Explanation
Due to its amphiphilic nature (having both hydrophilic and hydrophobic parts), 1,3-Benzenedimethanol, 2-hydroxy-5-nonyl- is widely used in various industries for different purposes, such as stabilizing mixtures, reducing surface tension, and preventing corrosion.
Explanation
The hydroxyl groups make the compound partially soluble in water due to hydrogen bonding, while the nonyl side chain increases its solubility in organic solvents.
Explanation
The compound is a liquid at room temperature due to the presence of the nonyl side chain, which provides a low melting and boiling point.
Explanation
As a nonionic surfactant, the compound does not dissociate into ions in water. It helps to lower the surface tension of liquids, allowing them to spread more easily and mix with other substances.
Explanation
Although the compound is used in personal care products, it can cause skin and eye irritation if not properly formulated or if it comes into direct contact with sensitive areas.
Explanation
As with many chemicals, 1,3-Benzenedimethanol, 2-hydroxy-5-nonylcan be harmful to aquatic life if released into the environment in significant quantities. Proper disposal and handling are essential to minimize environmental impact.
Explanation
The use and concentration of 1,3-Benzenedimethanol, 2-hydroxy-5-nonyl- in various products may be regulated by different agencies, such as the Environmental Protection Agency (EPA) or the European Chemicals Agency (ECHA), depending on the specific application and potential environmental impact.
Functional Groups
Hydroxyl (OH) groups and nonyl side chain
Applications
Surfactants, emulsifiers, personal care products, industrial applications, household cleaning products, and corrosion inhibitors
Solubility
Soluble in organic solvents, partially soluble in water
Physical State
Liquid at room temperature
Nonionic Surfactant
Reduces surface tension and improves wetting and dispersing properties
Safety
May cause skin and eye irritation
Environmental Impact
Potentially harmful to aquatic life
Regulatory Status
Subject to regulations depending on the application and concentration
Check Digit Verification of cas no
The CAS Registry Mumber 14165-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,6 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14165-64:
(7*1)+(6*4)+(5*1)+(4*6)+(3*5)+(2*6)+(1*4)=91
91 % 10 = 1
So 14165-64-1 is a valid CAS Registry Number.
14165-64-1Relevant academic research and scientific papers
Formaldehyde condensate of alkylphenol ethoxylate esters and preparation method of formaldehyde condensate
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Paragraph 0054-0055, (2017/08/31)
The invention provides a formaldehyde condensate of alkylphenol ethoxylate esters and a preparation method of the formaldehyde condensate and belongs to the technical field of sedimentation of catalytic cracking oil slurry. The formaldehyde condensate of
