Patent classifications
C09B67/0096
Pigment preparations
The novel pigment preparations containing at least one metal azo pigment A) and at least one aliphatic monocarboxylic acid B) having 10 to 22 carbon atoms are suitable for the colouring of plastics and in this connection feature improved heat stability.
Gardenia blue pigment with high brightness and low redness and a preparation method therefor
The invention discloses a gardenia blue pigment with high brightness and low redness and a preparation method therefor, and belongs to the technical field of pigment extraction. Genipin, an enzymolysis product of gardenia extract, is used as a raw material. Genipin and amino acids (phenylalanine, tryptophan, glycine, or tyrosine) are weighed at a molar ratio of 1:(0.375-0.75), and subjected to a polymerization reaction under a conventional condition to generate a gardenia blue precursor. The gardenia blue precursor is oxidized to develop a color, refined by using ultrafiltration membrane, and finally spray-dried to obtain the gardenia blue pigment with high brightness, low redness, and low cost.
NON- MUTAGENIC PHOTO CHROMIC DYE
A method of solubilizing a composition, such as an organic manufactured photochromic dye that is free of carcinogens, non-mutagenic, non-toxic to human skin in any concentration, and suitable for application to, and absorbable by, human skin. The photochromic dye is suitable to be applied directly to human skin, and which dye is configured to indicate exposure to UV rays. The composition is configured to change color upon exposure to UVA, UVB and/or UVC rays. The composition can be used with other compositions, such as sunscreen, and be applied to human skin prior to application of the sunscreen, or, formulated with the sunscreen such that when the active ingredients of the sunscreen diminish, the photochromic dye will change color to generate a visual indicator of this condition.
Azo dye composition and method for producing same
Provided are an azo dye composition including an azo dye compound represented by Formula (I) and a urea compound represented by Formula (II), and a method for producing an azo dye composition. R.sup.11, R.sup.12, R.sup.13 and R.sup.14 each independently represent a hydrogen atom, a halogen atom, or an aliphatic group; R.sup.15 represents an aliphatic group; R.sup.21 and R.sup.22 each independently represent a hydrogen atom, an aliphatic group, or an aromatic group; and n represents an integer from 0 to 2. ##STR00001##
METHODS OF SYNTHESIS AND/OR PURIFICATION OF DIAMINOPHENOTHIAZINIUM COMPOUNDS
Disclosed are methods of synthesis and/or purification of certain 3,7-diamino-phenothiazin-5-ium compounds (diaminophenothiazinium compounds) including Methylthioninium Chloride (MTC) (Methylene Blue), and the resulting high purity characterized by a purity greater than 98%, and very low levels of heavy metals and organic impurities Azure A, B, C and MVB. Also disclosed are methods of treatment of a tauopathy or methemoglobinemia in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of the high-purity diaminophenothiazinium compound.
Method of solubilizing a composition of a cleaned photochromic dye suitable for use on human skin
A method of solubilizing a composition, such as an organic manufactured photochromic dye that is free of carcinogens, non-mutagenic, non-toxic to human skin in any concentration, and suitable for application to, and absorbable by, human skin. The photochromic dye is suitable to be applied directly to human skin, and which dye is configured to indicate exposure to UV rays. The composition is configured to change color upon exposure to UVA, UVB and/or UVC rays. The composition can be used with other compositions, such as sunscreen, and be applied to human skin prior to application of the sunscreen, or, formulated with the sunscreen such that when the active ingredients of the sunscreen diminish, the photochromic dye will change color to generate a visual indicator of this condition.
METHOD OF SEPARATING BETANIN FROM RED QUINOA BY SUPERCRITICAL FLUID FRACTIONATION
The present invention relates to a method of separating betanin from red quinoa by supercritical fluid fractionation, including: mixing an extract of red quinoa with an ethanol/water mixture to obtain a mixture of red quinoa/ethanol/water; and separating betanin from the mixture of red quinoa/ethanol/water by supercritical fluid fractionation, which operates under a pressure between 2300 to 4400 psi at a temperature between 35 to 65 C. for a period of time between 15 to 90 minutes.
Methods of synthesis and/or purification of diaminophenothiazinium compounds
Disclosed are methods of synthesis and/or purification of certain 3,7-diamino-phenothiazin-5-ium compounds (diaminophenothiazinium compounds) including Methylthioninium Chloride (MTC) (Methylene Blue), and the resulting high purity characterized by a purity greater than 98%, and very low levels of heavy metals and organic impurities Azure A, B, C and MVB. Also disclosed are methods of treatment of a tauopathy or methemoglobinemia in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of the high-purity diaminophenothiazinium compound.
NATURAL COLORANTS AND PROCESSES OF MAKING THE SAME
The present invention is directed towards natural colorants comprising a material selected from the group consisting of genipin, purified genipin, pre-genipin compounds, iridoid compounds, genipin derivatives, a genipin-containing substance, and combinations of any thereof; and a primary amine containing compound. Processes of making natural colorants are further disclosed. Additionally, processes of producing a desired color of natural colorants are disclosed.
AZO DYE COMPOSITION AND METHOD FOR PRODUCING SAME
Provided are an azo dye composition including an azo dye compound represented by Formula (I) and a urea compound represented by Formula (II), and a method for producing an azo dye composition. R.sup.11, R.sup.12, R.sup.13 and R.sup.14 each independently represent a hydrogen atom, a halogen atom, or an aliphatic group; R.sup.15 represents an aliphatic group; R.sup.21 and R.sup.22 each independently represent a hydrogen atom, an aliphatic group, or an aromatic group; and n represents an integer from 0 to 2.
##STR00001##