22303-30-6 Usage
Uses
Used in Personal Care Products:
Triclocarban is used as a preservative in personal care products such as soaps and lotions for its ability to inhibit the growth of bacteria and fungi, thereby extending the shelf life and maintaining the hygienic quality of these products.
Used in Cosmetics Industry:
In the cosmetics industry, triclocarban is utilized as an antimicrobial agent to prevent the proliferation of microorganisms that could spoil the product or cause infections. Its inclusion helps ensure the safety and efficacy of cosmetic products over time.
However, it is important to note that due to the concerns regarding triclocarban's environmental and health impact, there has been a shift towards finding and using alternative preservatives that are more eco-friendly and have a lower risk profile.
Check Digit Verification of cas no
The CAS Registry Mumber 22303-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,0 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22303-30:
(7*2)+(6*2)+(5*3)+(4*0)+(3*3)+(2*3)+(1*0)=56
56 % 10 = 6
So 22303-30-6 is a valid CAS Registry Number.
22303-30-6Relevant academic research and scientific papers
A novel synthesis of isocyanates and ureas via β-elimination of haloform
Braverman,Cherkinsky,Kedrova,Reiselman
, p. 3235 - 3238 (2007/10/03)
A novel synthesis of isocyanates via base-induced β-elimination of haloform from N-monosubstituted trihaloacetamides is described. The rate of reaction exhibits a strong dependence on the nature of the trihalomethyl group. Thus, while the reaction of tribromoacetamides proceeds at room temperature and the reaction of trichloroacetamides requires heating in polar solvents, no reaction could be observed for any of the corresponding trifluoro derivatives. This novel β-elimination of haloform from stable and readily available trihaloacetamides was applied to a 'one-pot' synthesis of ureas which avoids the use of phosgene and isolation of isocyanates.
