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4-Chloro-3-methoxyphenol, also known as para-chloro-meta-cresol (PCMC), is a chlorophenol chemical compound characterized by its colorless to pale yellow crystalline solid form and a slightly phenolic odor. It is recognized for its broad-spectrum antimicrobial properties, making it a versatile component in various applications across different industries.

18113-07-0

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18113-07-0 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-3-methoxyphenol is used as an antiseptic and disinfectant for its effectiveness against a wide range of bacteria and fungi. It is incorporated into products such as hand sanitizers, soaps, and surgical scrubs to ensure hygienic conditions and prevent the spread of infections.
Used in Cosmetics Industry:
In the cosmetics industry, 4-Chloro-3-methoxyphenol serves as a preservative to maintain the integrity and safety of products by inhibiting the growth of microorganisms that could spoil the formulation or pose a risk to consumer health.
Used in Personal Care Products:
4-Chloro-3-methoxyphenol is utilized in personal care products to provide antimicrobial protection, ensuring that these products remain free from harmful microorganisms, thus enhancing their safety and efficacy for consumers.
These applications highlight the importance of 4-Chloro-3-methoxyphenol in maintaining cleanliness and preventing microbial contamination in various consumer products, contributing to public health and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 18113-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18113-07:
(7*1)+(6*8)+(5*1)+(4*1)+(3*3)+(2*0)+(1*7)=80
80 % 10 = 0
So 18113-07-0 is a valid CAS Registry Number.

18113-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-3-methoxyphenol

1.2 Other means of identification

Product number -
Other names X4399

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:18113-07-0 SDS

18113-07-0Relevant articles and documents

Derivatives of m-Guaiacol, Their Preparation and Their Uses

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Paragraph 0125; 0190, (2021/11/05)

The invention concerns derivatives of m-guaiacol, their preparation and their uses as biocides, in particular as antibacterials or disinfectants.

NOVEL HETEROCYCLIC COMPOUNDS AS PESTICIDES

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Paragraph 0699-0702, (2020/03/09)

The invention relates to novel compounds of the formula (I) in which Z, Y, A1, A2, A3, A4, X, R7, R8 and R9 have the meanings mentioned above, and processes and intermediates for the preparation thereof, and their use for controlling animal pests, in particular insects.

SUBSTITUTED-N-HETEROARYL COMPOUNDS AND USES THEREOF

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Page/Page column 97-98, (2020/01/24)

The present disclosure relates generally to compounds useful for the treatment and/or enhancement of cognitive function and negative symptoms associated with central nervous system disorders where the circuitry involving fast spiking PV+ interneurons and the production of cortical gamma oscillations is disrupted. The subject disclosure enables the manufacture of medicaments as well as compositions containing same for use in methods of therapy and prophylaxis of cognitive dysfunction and negative symptoms.

Practical regioselective halogenation of vinylogous esters: Synthesis of differentiated mono-haloresorcinols and polyhalogenated resorcinols

Chen, Xiaohong,Liu, Xiaoguang,Martinez, Jenny S.,Mohr, Justin T.

, p. 3653 - 3665 (2016/06/06)

A practical and efficient method for the direct, regioselective conversion of vinylogous esters to haloresorcinols is reported. Control of the reaction conditions enables synthesis of either the 4- or 6-haloresorcinol isomers from a common precursor with excellent regiocontrol and high yield. The generality and functional group tolerance of this novel protocol is demonstrated. The utility of this methodology to access polyhaloresorcinols is also reported. These methods create useful functionalized building blocks for further synthetic applications.

A photochemical route to 2-substituted benzo[b]furans

Protti, Stefano,Fagnoni, Maurizio,Albini, Angelo

experimental part, p. 6473 - 6479 (2012/10/08)

2-Substituted benzo[b]furans were synthesized by a one-step metal-free photochemical reaction between 2-chlorophenol derivatives and terminal alkynes by tandem formation of an aryl-C and a C-O bond via an aryl cation intermediate. The mild conditions and the application to chlorophenols rather of the more expensive bromo or iodo analogues makes this procedure environmentally convenient.

Synthesis and evaluation of self-calibrating ratiometric viscosity sensors

Yoon, Hyung-Jo,Dakanali, Marianna,Lichlyter, Darcy,Chang, Willy M.,Nguyen, Karen A.,Nipper, Matthew E.,Haidekker, Mark A.,Theodorakis, Emmanuel A.

, p. 3530 - 3540 (2011/06/25)

We describe the design, synthesis and fluorescent profile of a family of self-calibrating dyes that provide ratiometric measurements of fluid viscosity. The design is based on covalently linking a primary fluorophore (reference) that displays a viscosity-independent fluorescence emission with a secondary fluorophore (sensor) that exhibits a viscosity-sensitive fluorescence emission. Characterization of fluorescent properties was made with separate excitation of the units and through Resonance Energy Transfer from the reference to the sensor dye. The chemical structures of both fluorophores and the linker length have been evaluated in order to optimize the overall brightness and sensitivity of the viscosity measurements. We also present an application of such ratiometric dyes for the detection of membrane viscosity changes in a liposome model.

SUBSTITUTED BENZYLIMIDAZOLES USEFUL FOR THE TREATMENT OF INFLAMMATORY DISEASES

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Page/Page column 57, (2008/06/13)

The invention comprises a class of derivatives of substituted benzylimidazoles of the formula (I) and methods for making the same. These compounds are useful for the treatment of inflammatory conditions.

Hydroxyacetic acid derivatives for the treatment of diabetic complications

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, (2008/06/13)

Racemic and chiral (2R,4R)-4-c-hydroxy-2-4-(substituted)chroman(and thiochroman)-4-acetic acids and their pharmaceutically acceptable salts, their use in the treatment of diabetic complications and intermediates therefor.

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