90481-44-0 Usage
Chemical structure
A derivative of resorcinol and benzothiazole
Applications
a. Hair dyes
b. Skin whitening products
c. Cosmetics and personal care products
d. UV-absorbing sunscreen formulations
Properties
a. Antioxidant
b. Antimicrobial
Mechanism of action
Inhibits the production of melanin, acting as an effective skin-lightening agent
Potential uses
Treatment of inflammatory skin conditions
Safety concerns
Regulatory restrictions in some regions due to potential health risks associated with high concentrations
Molecular weight
258.3 g/mol (calculated from the chemical formula)
Appearance
Likely a solid, based on its use in various formulations
Solubility
Not explicitly mentioned, but likely soluble in organic solvents due to its chemical structure
Stability
Stable under normal conditions, but specific stability information is not provided in the material
Reactivity
No specific reactivity information provided, but its use as an antioxidant suggests it may be reactive with certain substances under certain conditions
Environmental impact
No specific information provided, but as a chemical compound used in the cosmetic industry, it may have potential environmental implications if not properly managed or disposed of.
Check Digit Verification of cas no
The CAS Registry Mumber 90481-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,8 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90481-44:
(7*9)+(6*0)+(5*4)+(4*8)+(3*1)+(2*4)+(1*4)=130
130 % 10 = 0
So 90481-44-0 is a valid CAS Registry Number.
90481-44-0Relevant academic research and scientific papers
Solid-state Fluorescent Photophysics of Some 2-Substituted Benzothiazoles
Anthony, Kevin,Brown, Robert G.,Hepworth, John D.,Hodgson, Kevin W.,May, Bernadette,West, Michael A.
, p. 2111 - 2118 (2007/10/02)
The solid-state fluorescence properties of a series of benzothiazoles with phenyl, napthalene, and coumarin moieties substituted at the 2-position have been investigated.The necessity for a 2'-OH substituent for fluorescence has been confirmed and the effects of further substitution in the 2-phenyl ring are reported.
