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5153-25-3

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  • China Biggest Factory Manufacturer Supply 2-Ethylhexyl 4-hydroxybenzoate CAS 5153-25-3

    Cas No: 5153-25-3

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5153-25-3 Usage

General Description

2-Ethylhexyl 4-hydroxybenzoate, also known as octyl 4-hydroxybenzoate or EHG, is a chemical compound commonly used as a preservative in cosmetics and personal care products. It acts as a broad-spectrum UV filter and helps to protect the skin and hair from the damaging effects of sunlight. EHG is also used as an antimicrobial agent in various products, helping to extend their shelf life by inhibiting the growth of bacteria and fungi. Despite its widespread use, some concerns have been raised about the potential endocrine-disrupting effects of EHG, prompting calls for further research into its safety and potential health impacts.

Check Digit Verification of cas no

The CAS Registry Mumber 5153-25-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,5 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5153-25:
(6*5)+(5*1)+(4*5)+(3*3)+(2*2)+(1*5)=73
73 % 10 = 3
So 5153-25-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O3/c1-3-5-6-12(4-2)11-18-15(17)13-7-9-14(16)10-8-13/h7-10,12,16H,3-6,11H2,1-2H3

5153-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethylhexyl 4-Hydroxybenzoate

1.2 Other means of identification

Product number -
Other names Octylparaben

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:5153-25-3 SDS

5153-25-3Synthetic route

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

2-ethyl-1-hexyl p-hydroxybenzoate
5153-25-3

2-ethyl-1-hexyl p-hydroxybenzoate

Conditions
ConditionsYield
With sulfuric acid; benzene Entfernen des entstehenden Wassers;
4-bromo-phenol
106-41-2

4-bromo-phenol

2-Ethylhexyl alcohol
104-76-7

2-Ethylhexyl alcohol

2-ethyl-1-hexyl p-hydroxybenzoate
5153-25-3

2-ethyl-1-hexyl p-hydroxybenzoate

Conditions
ConditionsYield
With sodium carbonate; palladium-carbon
sulphur dichloride

sulphur dichloride

zinc chloride anhydrate

zinc chloride anhydrate

2-ethyl-1-hexyl p-hydroxybenzoate
5153-25-3

2-ethyl-1-hexyl p-hydroxybenzoate

3,3'-thiobis(2-ethylhexyl p-hydroxybenzoate)

3,3'-thiobis(2-ethylhexyl p-hydroxybenzoate)

Conditions
ConditionsYield
In chloroform
formaldehyd
50-00-0

formaldehyd

para-tert-butylphenol
98-54-4

para-tert-butylphenol

2-ethyl-1-hexyl p-hydroxybenzoate
5153-25-3

2-ethyl-1-hexyl p-hydroxybenzoate

poly(2,2-bis(4-hydroxyphenyl)propane-co-p-t-butylphenol-co-2-ethylhexyl 4-hydroxybenzoate-co-formaldehyde)

poly(2,2-bis(4-hydroxyphenyl)propane-co-p-t-butylphenol-co-2-ethylhexyl 4-hydroxybenzoate-co-formaldehyde)

Conditions
ConditionsYield
With potassium hydroxide In water; xylene for 8h; Heating / reflux;
formaldehyd
50-00-0

formaldehyd

para-tert-butylphenol
98-54-4

para-tert-butylphenol

2-ethyl-1-hexyl p-hydroxybenzoate
5153-25-3

2-ethyl-1-hexyl p-hydroxybenzoate

1,1-bis-(4-hydroxy-phenyl)-1-phenyl-propane
47252-81-3

1,1-bis-(4-hydroxy-phenyl)-1-phenyl-propane

poly(4,4'-(1-phenylethylidene)bisphenol-co-p-t-butylphenol-co-co-2-ethylhexyl 4-hydroxybenzoate-co-formaldehyde)

poly(4,4'-(1-phenylethylidene)bisphenol-co-p-t-butylphenol-co-co-2-ethylhexyl 4-hydroxybenzoate-co-formaldehyde)

Conditions
ConditionsYield
With potassium hydroxide In water; xylene for 8h; Heating / reflux;
formaldehyd
50-00-0

formaldehyd

1,1-bis(4-hydroxyphenyl)cyclohexane
843-55-0

1,1-bis(4-hydroxyphenyl)cyclohexane

para-tert-butylphenol
98-54-4

para-tert-butylphenol

2-ethyl-1-hexyl p-hydroxybenzoate
5153-25-3

2-ethyl-1-hexyl p-hydroxybenzoate

poly(1,1-bis(4-hydroxyphenyl)cyclohexane-co-p-t-butylphenol-co-formaldehyde)

poly(1,1-bis(4-hydroxyphenyl)cyclohexane-co-p-t-butylphenol-co-formaldehyde)

Conditions
ConditionsYield
With potassium hydroxide In water; xylene for 8h; Heating / reflux;

5153-25-3Downstream Products

5153-25-3Relevant articles and documents

Method for the manufacture of hydroxy aromatic monocarboxylic acids

-

, (2008/06/13)

A method for preparing hydroxy aromatic carboxylic acids, or the ester derivatives thereof, comprises the carbonylation of a hydroxy aromatic bromide in the presence of a catalytic amount of a transition element of group VIII of the Periodic Table on a carbon support, at a pH of above 8, in the absence of any promoter.The reaction is carried out at a temperature in the range of between 140oC to 200oC. The resulting products are obtained in high yields and of high purity. The method has particular applicability to the manufacture of 6-carboxy-2-naphthol and 4-hydroxy-4'-carboxy-biphenyl.

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