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133-53-9

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133-53-9 Usage

Description

2,4-Dichloro-3,5-dimethylphenol is a chemical compound characterized by its light beige powder appearance and a phenolic characteristic odor. It is a white to off-white powder or block mass powder with a minimum content of active matter at 98.0%. 2,4-Dichloro-3,5-dimethylphenol has a melting range of 92-95°C and a boiling point of 269°C. It is sparingly soluble in water at 20°C with a solubility of 0.2g/L. The dry loss is maximum at 0.10%, and it contains a maximum of 80 ppm iron, 0.5% maximum residue on ignition, 0.5% maximum water content, and 0.001% maximum total heavy metal. The solubility of 2,4-Dichloro-3,5-dimethylphenol results in a clear solution.

Uses

Used in Soap Industry:
2,4-Dichloro-3,5-dimethylphenol is used as a bacteriostat in soaps, helping to inhibit the growth of bacteria and maintain cleanliness.
Used as a Mold Inhibitor and Preservative:
2,4-Dichloro-3,5-dimethylphenol serves as a mold inhibitor and preservative in various applications, preventing the growth of mold and preserving the quality of products.
Used in Aqueous Functional Fluids:
2,4-Dichloro-3,5-dimethylphenol is used as a preservative in aqueous functional fluids, ensuring the stability and longevity of these fluids.
Used as a Microbicide in Disinfectants:
2,4-Dichloro-3,5-dimethylphenol is also used as a microbicide in disinfectants, helping to eliminate microorganisms and promote a hygienic environment. However, it is of lesser importance compared to PCMX due to its more intense smell and lower solubility in water.

Preparation

2,4-Dichloro-3,5-dimethylphenol is obtained by reaction of 4-chloro-3,5-dimethylphenol with N-chloroacetamide in glacial acetic acid with concentrated HCl.

Solubility in organics

2,4-Dichloro-3,5-dimethylphenol is soluble in alkali solutions, and readily soluble in organic solvents.

Solubility in water

It has a solubility in water of 0.2 g/L at 20 °C.

TEST ITEMS

SPECIFICATION

ODOUR

PHENOLIC CHARACTERISTIC ODOUR

CONTENT OF ACTIVE MATTER

98.0% min

MELT RANGE

92-95 ° C

BOILING POINT

269 ° C

SOLUBILITY 20 ° C/WATER

0.2g/L

DRY LOSS

0.10% max

IRON

80 ppm max

RESIDUE ON IGNITION

0.5% max

WATER

0.5% max

TOTAL HEAVY METAL

0.001% max

SOLUBILITY

CLEAR SOLUTION

Check Digit Verification of cas no

The CAS Registry Mumber 133-53-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133-53:
(5*1)+(4*3)+(3*3)+(2*5)+(1*3)=39
39 % 10 = 9
So 133-53-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Cl2O/c1-4-3-6(11)8(10)5(2)7(4)9/h3,11H,1-2H3

133-53-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Price
  • Detail
  • Alfa Aesar

  • (A17305)  2,4-Dichloro-3,5-dimethylphenol, 96%   

  • 133-53-9

  • 50g

  • 494.0CNY

  • Detail
  • Alfa Aesar

  • (A17305)  2,4-Dichloro-3,5-dimethylphenol, 96%   

  • 133-53-9

  • 250g

  • 1241.0CNY

  • Detail
  • Alfa Aesar

  • (A17305)  2,4-Dichloro-3,5-dimethylphenol, 96%   

  • 133-53-9

  • 1000g

  • 4083.0CNY

  • Detail

133-53-9SDS

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 2,4-Dichloro-3,5-dimethylphenol

1.2 Other means of identification

Product number -
Other names 2,4-dichloro-3,5-dimethyl phenol

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:133-53-9 SDS

133-53-9Synthetic route

N-chloroacetamide
598-49-2

N-chloroacetamide

4-Chloro-3,5-dimethylphenol
88-04-0

4-Chloro-3,5-dimethylphenol

2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

Conditions
ConditionsYield
With hydrogenchloride; acetic acid
3,5-Dimethylphenol
108-68-9

3,5-Dimethylphenol

2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

Conditions
ConditionsYield
With sulfuryl dichloride; chloroform
With hydrogenchloride; manganese(II) sulfate; dihydrogen peroxide In water at 80℃;86 %Chromat.
3,5-Dimethylphenol
108-68-9

3,5-Dimethylphenol

A

4-Chloro-3,5-dimethylphenol
88-04-0

4-Chloro-3,5-dimethylphenol

B

2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

Conditions
ConditionsYield
With N-chlorotriethylammonium chloride In trifluoroacetic acid Ambient temperature; Yield given. Yields of byproduct given;
chloroform
67-66-3

chloroform

3,5-Dimethylphenol
108-68-9

3,5-Dimethylphenol

sulfuryl chloride (2 mol)

sulfuryl chloride (2 mol)

2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

3,5-Dimethylphenol
108-68-9

3,5-Dimethylphenol

A

4-Chloro-3,5-dimethylphenol
88-04-0

4-Chloro-3,5-dimethylphenol

B

2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

C

o-chloro-m-xylenol
5538-41-0

o-chloro-m-xylenol

Conditions
ConditionsYield
With iron(III) chloride; sulfuryl dichloride; 1,3-bis(methylthio)propane In dichloromethane at 20℃; for 4h; Reagent/catalyst; regioselective reaction;A 75 %Chromat.
B 9 %Chromat.
C 10 %Chromat.
2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

methyl iodide
74-88-4

methyl iodide

2,4-dichloro-3,5-dimethylanisole
23400-00-2

2,4-dichloro-3,5-dimethylanisole

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide at 20℃;95%
2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

2,4,6-trichloro-3,5-dimethyl-phenol
6972-47-0

2,4,6-trichloro-3,5-dimethyl-phenol

Conditions
ConditionsYield
With chlorine
2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

2-bromo-4,6-dichloro-3,5-dimethyl-phenol
874519-00-3

2-bromo-4,6-dichloro-3,5-dimethyl-phenol

Conditions
ConditionsYield
With bromine; acetic acid
2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

2,4-dichloro-6-iodo-3,5-dimethyl-phenol

2,4-dichloro-6-iodo-3,5-dimethyl-phenol

Conditions
ConditionsYield
With Iodine monochloride; acetic acid
2,4-dichloro-3,5-dimethylphenol
133-53-9

2,4-dichloro-3,5-dimethylphenol

4-Methylbenzyl chloride
104-82-5

4-Methylbenzyl chloride

(2,4-dichloro-3,5-dimethyl-phenyl)-(4-methyl-benzyl)-ether

(2,4-dichloro-3,5-dimethyl-phenyl)-(4-methyl-benzyl)-ether

133-53-9Relevant articles and documents

Regioselective synthesis of important chlorophenols in the presence of methylthioalkanes with remote SMe, OMe or OH substituents

Smith, Keith,Al-Zuhairi, Ali J.,Elliott, Mark. C.,El-Hiti, Gamal A.

, p. 607 - 621 (2018/07/13)

Various methylthio alcohols, methoxy(methylthio)alkanes and bis(methylthio)alkanes have been used as regioselectivity modifiers in the chlorination reactions of various phenols at room temperature. The process involves the use of a slight excess of sulfuryl chloride in the presence of aluminum or ferric chloride as an activator. Methylthio alcohols, methoxy(methylthio)alkanes and bis(methylthio)alkanes having 2 and 3 methylene groups as a spacer were found to be good for the para-selective chlorination of o-cresol and phenol. On the other hand, methylthio alcohols, methoxy(methylthio)alkanes and bis(methylthio)alkanes having 6 and 9 methylene groups were found to be good for the selective para-chlorination of m-xylenol and m-cresol. Calculations using density functional theory on bis(methylthio)alkanes have suggested two different types of stable chlorinated intermediates depending on the number of methylene units as a spacer.

Method of disinfecting premises from coccidial oocysts using generated ammonia

-

, (2008/06/13)

A method of disinfecting premises from coccidial oocysts in which surface to be disinfected is thoroughly wetted with a first aqueous solution of ammonium salt containing approximately 0.5 to 1.5 molar of ammonium together with non-ionic surfactant and indicator having a color change in the region of pH 8 to pH 10 and the wetted surface is then covered with sufficient of a second aqueous solution of alkali metal hydroxide containing approximately 0.75 to 2.3 molar of hydroxide toether with phenolic bactericide to cause the indicator to change color on the treated surface. A preparation for use in such a method comprises a first package containing ammonium salt together with non-ionic surfactant and indicator and second package containing alkali metal hydroxide and phenolic bactericide, the molar amount of hydroxide in the second package being greater than the molar amount of ammonium in the first package.

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