Welcome to LookChem.com Sign In|Join Free

CAS

  • or
3-Chloro-4-(hydroxyMethyl)phenol, also known as PCMX, is a chemical compound with potent antimicrobial properties. It is characterized by its ability to disrupt the cell walls of bacteria and inhibit their growth and reproduction, making it a versatile and effective agent against a broad spectrum of microorganisms. PCMX is commonly utilized in various personal care products, medical settings, and pharmaceutical products due to its efficacy and safety when used appropriately.

171569-42-9

Post Buying Request

171569-42-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

171569-42-9 Usage

Uses

Used in Personal Care Products:
3-Chloro-4-(hydroxyMethyl)phenol is used as an antiseptic and disinfectant in personal care products such as soaps, lotions, and hand sanitizers for its ability to effectively eliminate bacteria and other microorganisms, promoting hygiene and preventing the spread of infections.
Used in Medical Settings:
In the medical industry, 3-Chloro-4-(hydroxyMethyl)phenol is used as a surgical scrub to ensure a sterile environment during surgical procedures. Its antimicrobial properties help reduce the risk of postoperative infections and promote faster healing.
Used as a Preservative in Pharmaceutical Products:
3-Chloro-4-(hydroxyMethyl)phenol is used as a preservative in pharmaceutical products to prevent the growth of microorganisms and maintain the stability and efficacy of the medication. Its broad-spectrum antimicrobial activity ensures the safety and quality of pharmaceutical products.
However, it is important to note that excessive exposure to 3-Chloro-4-(hydroxyMethyl)phenol can cause skin irritation and allergic reactions in some individuals. Therefore, it should be used with caution and in accordance with safety guidelines to minimize potential adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 171569-42-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,5,6 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 171569-42:
(8*1)+(7*7)+(6*1)+(5*5)+(4*6)+(3*9)+(2*4)+(1*2)=149
149 % 10 = 9
So 171569-42-9 is a valid CAS Registry Number.

171569-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-4-(hydroxymethyl)phenol

1.2 Other means of identification

Product number -
Other names 3-chloro-4-(hydroxymethyl)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:171569-42-9 SDS

171569-42-9Relevant articles and documents

TYROSINE KINASE INHIBITOR AND PHARMACEUTICAL COMPOSITION COMPRISING SAME

-

Paragraph 0332; 0334, (2018/03/25)

The present invention relates to a tyrosine kinase inhibitor and a pharmaceutical composition comprising same. The tyrosine kinase inhibitor of the present invention has the structures as shown in the following formula (I) or (II):

N-PYRAZOLYL CARBOXAMIDES AS CRAC CHANNEL INHIBITORS

-

Page/Page column 53, (2010/11/05)

The present invention relates to amide compounds, processes for their preparation, pharmaceutical compositions containing these compounds and to their use in the treatment of disorders, conditions or disorders such as allergic disorders, inflammatory disorders and disorders of the immune system.

Acetals as New 2′-O-Protecting Functions for the Synthesis of Oligoribonucleotides: Synthesis of Uridine Building Blocks and Evaluation of Their Relative Acid Stability

Matysiak, Stefan,Fitznar, Hans-Peter,Schnell, Ralf,Pfleiderer, Wolfgang

, p. 1545 - 1566 (2007/10/03)

A broad variety of new acyclic vinyl ethers (see 6-41) have been synthesized via the vinyl-interchange reaction of ethyl vinyl ether at room temperature using mercury(II) trifluoroacetate as a highly efficient catalyst. The appropriate vinyl ethers were r

Solid-phase synthesis of oligoribonucleotides

-

, (2008/06/13)

A process for the preparation of oligoribonucleotides of the formula STR1 in which n, L, BB, W, T, Y', U, C1 and C2 are as defined in the description, by solid-phase synthesis is described, as are intermediates of the oligoribonucleo

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 171569-42-9