90604-34-5 Usage
Main Properties
1. Emollient: Alcohols, C20-22 act as emollients, softening and smoothing the skin.
2. Emulsifier: They function as emulsifiers, helping to blend water and oil-based ingredients in skincare products.
3. Derived from Natural Sources: These alcohols are derived from natural sources such as vegetable oils.
4. Moisture Barrier: They provide a barrier on the skin to prevent moisture loss.
5. Safe for Cosmetics: Generally considered safe for cosmetic use.
6. Non-irritating: Known for their non-irritating properties, suitable for all skin types.
7. Non-sensitizing: Also non-sensitizing, making them suitable for sensitive skin.
8. Long Shelf Life: They have a long shelf life.
9. Resistance to Oxidation: Resistant to oxidation, ensuring stability in formulations.
Specific Content
1. Function: Primarily used as emollients and emulsifiers.
2. Source: Derived from natural sources like vegetable oils.
3. Applications: Found in moisturizers, creams, lotions, and other personal care products.
4. Effectiveness: Effective in softening and smoothing the skin.
5. Safety: Generally considered safe for use in cosmetics.
6. Suitability: Suitable for all skin types, including sensitive skin.
7. Shelf Life: Have a long shelf life.
8. Stability: Resistant to oxidation, ensuring stability in formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 90604-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,0 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90604-34:
(7*9)+(6*0)+(5*6)+(4*0)+(3*4)+(2*3)+(1*4)=115
115 % 10 = 5
So 90604-34-5 is a valid CAS Registry Number.
90604-34-5Relevant articles and documents
Benzylated 1,2,3-triazoles as anticoccidiostats
Bochis,Chabala,Harris,Peterson,Barash,Beattie,Brown,Graham,Waksmunski,Tischler,Joshua,Smith,Colwell,Wyvratt Jr.,Fisher,Tamas,Nicolich,Schleim,Wilks
, p. 2843 - 2852 (2007/10/02)
Substituted 5-amino-4-carbamoyl-1,2,3-triazoles 3a-w were prepared by two synthetic schemes and evaluated in vivo for anticoccidial activity. Both schemes proceeded by brominating appropriately substituted toluenes 4a-s,v to 5a-s,v. In Scheme I, the brominated benzyl analogues 5 were converted to the corresponding benzyl azides 6, which were treated with cyanoacetamide to yield 1-substituted-5-amino-4-carbamoyl-1,2,3-triazoles 3. In Scheme II, the benzyl halides 5 were employed to alkylate the sodium salt of 5-amino-4-carbamoyl-1,2,3-triazole (7). Preliminary screening data against Eimeria acervulina and E. tenella in chickens suggested structural requirements for maximizing activity. Further evaluation against a relatively resistant series of eight Eimeria field isolates revealed L-651,582 (3a) to be a highly effective coccidiostat. However, unacceptable tissue residues precluded further development. Mechanistic studies on this series of 5-amino-4-carbamoyl-1,2,3-triazoles and, in particular, on L-651,582 (3a) revealed that its mode of action does not involve inhibition of IMP dehydrogenase, but probably interferes with host cell calcium entry. In addition, L-651,582 has been found to have antiproliferative activity in several disease models and was recently reported to possess antimetastatic activity in a model of ovarian cancer progression.
