13481-70-4 Usage
General Description
2,6-dichloro-m-cresol is a chemical compound that is commonly used as a preservative in various personal care products, including soaps, lotions, and cosmetics. It is a white to light brown crystalline solid with a sweet, phenolic odor. 2,6-dichloro-m-cresol is effective against a wide range of microorganisms, including bacteria and fungi, making it useful for preventing spoilage and contamination in these products. However, 2,6-dichloro-m-cresol has also been associated with skin irritation and sensitization in some individuals, leading to restrictions on its use in certain formulations. Additionally, this compound has been classified as a possible human carcinogen, raising concern about its potential long-term health effects. As a result, regulatory agencies have set limits on the concentration of 2,6-dichloro-m-cresol that can be used in products intended for human use.
Check Digit Verification of cas no
The CAS Registry Mumber 13481-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13481-70:
(7*1)+(6*3)+(5*4)+(4*8)+(3*1)+(2*7)+(1*0)=94
94 % 10 = 4
So 13481-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl2O/c1-4-2-3-5(8)7(10)6(4)9/h2-3,10H,1H3
13481-70-4Relevant articles and documents
Investigations of the reactions of monochloramine and dichloramine with selected phenols: Examination of humic acid models and water contaminants
Heasley, Victor L.,Fisher, Audra M.,Herman, Erica E.,Jacobsen, Faith E.,Miller, Evan W.,Ramirez, Ashley M.,Royer, Nicole R.,Whisenand, Josh M.,Zoetewey, David L.,Shellhamer, Dale F.
, p. 5022 - 5029 (2008/04/18)
The phenols are an important area of investigation because they are substituents in the humic acids and are common contaminants in water. The reactivities and orientations of two common phenols (phenol and m-cresol), and some of their chlorinated intermediates with aqueous monochloroamine and dichloroamine were presented. m-Cresol was more reactive than phenol with both chlorinating agents. NH2Cl and NHCl2 showed extensive reactivity toward the phenols, even the partially chlorinated less reactive intermediates would be expected to fully chlorinate the activated positions in phenolic substituents in the humic acids.
