10486-48-3 Usage
Uses
Used in Pharmaceutical Industry:
4-amino-2,6-xylenol hydrochloride is used as a potential antioxidant and anti-inflammatory agent for its studied properties in medical applications, contributing to the development of treatments that may benefit from these characteristics.
Used in Cosmetic Industry:
4-amino-2,6-xylenol hydrochloride is used as a colorant and fragrance ingredient in hair dyes, hair care products, and skin care products, enhancing their aesthetic appeal and sensory experience for consumers.
Used in Hair Dye Products:
4-amino-2,6-xylenol hydrochloride is used as a colorant in hair dyes to provide a range of shades and improve the vibrancy and longevity of hair color.
Used in Hair Care Products:
In hair care products, 4-amino-2,6-xylenol hydrochloride is used as a colorant to enhance the appearance of hair and potentially contribute to the product's fragrance profile.
Used in Skin Care Products:
4-amino-2,6-xylenol hydrochloride is used as a colorant in skin care products to improve the visual appeal of the product and may also serve as a fragrance ingredient to provide a pleasant scent.
Check Digit Verification of cas no
The CAS Registry Mumber 10486-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10486-48:
(7*1)+(6*0)+(5*4)+(4*8)+(3*6)+(2*4)+(1*8)=93
93 % 10 = 3
So 10486-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-5-3-7(9)4-6(2)8(5)10/h3-4,10H,9H2,1-2H3
10486-48-3Relevant academic research and scientific papers
Synthesis and Characterization of Some Pyridinium-N-phenoxide Betaine Dyes for Secod-Harmonic Generation
Paley, M. Steven,Harris, J. Milton
, p. 568 - 574 (2007/10/02)
The synthesis and characterization of some pyridinium-N-phenoxide betaine dyes (including Reichhardt's dye) for second-harmonic generation (SHG) is described.These dyes are highly solvatochromic, which indicates that they can have large second-order molecular polarizabilities.The effects of substituents on the solvatochromic and optical properties of the betaines are investigated.Also the crystal structure of the betaines is discussed and the molecular geometry in the crystal is compared to that predicted by AM1 calculations.The crystallographic space group of the betaines is found to be centrosymmetric; therefore these dyes are incapable of SHG as crystals.To overcome this obstacle, we have synthesized and characterized a chiral betaine; because of its chirality this compound must necessarily crystallize in a noncentrosymmetric space group, thereby making it capable of SHG as a crystal.Lastly, the utility of these betaines for SHG in poled polymer films is discussed.
