CN110897165A - Conjugated zinc linoleate preparation and preparation method thereof - Google Patents

Conjugated zinc linoleate preparation and preparation method thereof Download PDF

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CN110897165A
CN110897165A CN201911404782.4A CN201911404782A CN110897165A CN 110897165 A CN110897165 A CN 110897165A CN 201911404782 A CN201911404782 A CN 201911404782A CN 110897165 A CN110897165 A CN 110897165A
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zinc
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linoleic acid
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刘康慨
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Shanxi Kairuisen Biotechnology Co Ltd
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/115Fatty acids or derivatives thereof; Fats or oils
    • A23L33/12Fatty acids or derivatives thereof
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    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/16Inorganic salts, minerals or trace elements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/20Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • A61K31/201Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having one or two double bonds, e.g. oleic, linoleic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/24Heavy metals; Compounds thereof
    • A61K33/30Zinc; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/02Nutrients, e.g. vitamins, minerals
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs

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Abstract

The invention discloses a conjugated linoleic acid zinc preparation and a preparation method thereof. The preparation is prepared from the following raw materials in molar ratio: conjugated linoleic acid: soluble zinc salt 2: 1.00-1.50; the preparation method is that under room temperature or near room temperature, conjugated linoleic acid with biological function activity is firstly saponified with alkali metal alcoholate or alkali metal hydroxide and then reacted with soluble zinc salt solution to obtain conjugated zinc linoleate; the method of the invention is homogeneous reaction, has simple process, simple and convenient operation, high product purity and stable property, and is particularly suitable for the application field with higher requirements on product quality.

Description

Conjugated zinc linoleate preparation and preparation method thereof
Technical Field
The invention relates to the technical field of nutrition supplementing preparations, in particular to a conjugated zinc linoleate preparation and a preparation method thereof.
Background
Conjugated linoleic acid was discovered in the end of the 80's 20 th century as a natural fatty acid with many important biological activities. Animal experiments show that the conjugated linoleic acid has the functions of reducing fat, increasing muscle, resisting cancer and atherosclerosis, enhancing the immunity of the body, improving the metabolism of bone tissues and the like. Conjugated linoleic acid, as a newly discovered nutrient, does not have the so-called homology problem because it is a secondary metabolite of animals, does not have the upper limit problem of use in principle, and is beneficial and harmless to the body when being frequently eaten. The conjugated linoleic acid with a certain dosage is added into the food, so that the deficiency of human body intake can be made up, the capability of resisting a plurality of diseases of the human body can be enhanced, and the immunity of the human body can be improved. At present, conjugated linoleic acid has become one of the research hotspots in the fields of medicines, functional foods and the like, and has been developed into health care products for reducing human body fat and increasing muscles abroad, and some capsule preparation products are put on the market, but the comprehensive development and deep processing utilization of the conjugated linoleic acid at home are blank, the raw materials of the products are easy to obtain, and the market prospect is wide.
Chinese patent CN1357406A discloses a microcapsule of conjugated linoleic acid. The product is composed of conjugated linoleic acid salt, other fatty acid salt, wall material, solvent and antioxidant, but the conjugated linoleic acid is difficult to be completely converted, and free conjugated linoleic acid or unreacted free alkali can be mixed in the product, so that the product is impure, and the quality stability of the product is influenced.
According to the research report of the Chinese disease prevention and control center nutrition and food safety institute, the zinc element is an indispensable trace element for human bodies and plays a vital role in life bodies. It is known that zinc is a component of more than 100 enzymes in the human body, and related biological enzymes play an important role in tissue respiration and metabolism of proteins, fats, sugars, nucleic acids, and the like; zinc deficiency can cause dwarfism, difficulty in healing of damaged tissues and influence on fetal development; can cause slow taste, anorexia, sexual maturation retardation, sexual organ hypoplasia, sexual hypofunction, hyposexuality, oligospermia, and abnormal menstruation; the zinc deficiency can cause the reduction of the proliferation of immune cells, the reduction of the activity of thymus and the change of cell surface receptors. In addition, zinc is helpful for removing cholesterol in vivo, preventing and treating atherosclerosis, and inhibiting canceration of cells. The causes of zinc deficiency can be summarized as congenital poor storage, intake deficiency and malabsorption. The zinc deficiency of the adolescent children is particularly common because the human body needs a large amount of zinc. Therefore, scientifically and effectively maintaining the zinc element balance of the human body is of great importance to the life body.
Inorganic zinc and small molecular organic zinc preparations in the current market have poor effect as food and drug supplement preparations, stimulate intestines and stomach, produce related side effects, and further need to improve quality and upgrade for generations. The absorption and utilization rate of inorganic zinc (zinc sulfate, zinc chloride, zinc nitrate and the like) is low (only 7%), and the gastrointestinal tract is easily stimulated to cause adverse reaction; the organic acid zinc (zinc gluconate, zinc glycyrrhizate, zinc acetate, zinc citrate, zinc amino acid, zinc lactate, etc.) has high zinc content, and can inhibit absorption of other microelements such as calcium and iron, and can cause calcium deficiency and anemia.
The bioaffinity zinc is the multifunctional conjugated zinc linoleate developed by the patent, has low zinc content which is almost equivalent to the zinc content of food, is absolutely safe, has no side effect on human bodies, and can be taken before meals. The food has high activity, can effectively promote the absorption and utilization of various nutrients by a human body, and can not antagonize the absorption of the nutrients such as calcium, iron and the like, thereby finally achieving the effect of supplementing various nutrients from diet of the human body. The biological affinity zinc, pure biological agent, high activity, easy absorption and quick effect. And is safe without any hormone and toxic and side effects, thereby being very beneficial to the absorption of calcium and other trace elements. After the zinc is biologically functionalized, the oxidation stability of the conjugated linoleic acid is improved, the stability and the usability are enhanced, and the functionality is increased. The composite high-grade nutriment, namely the conjugated linoleic acid is a novel multifunctional high-grade nutriment and can also be used as an important component preparation of food and medicines.
Disclosure of Invention
The invention aims to solve the technical problems and provide a conjugated zinc linoleate preparation with high product purity and stable product quality and a preparation method thereof.
In order to solve the technical problems, the technical scheme provided by the invention is as follows: a conjugated zinc linoleate preparation is prepared from the following raw materials in molar ratio: conjugated linoleic acid: soluble zinc salt 2: 1.00-1.50;
the conjugated linoleic acid zinc preparation is prepared by the steps of firstly saponifying a pure product of conjugated linoleic acid with biological functional activity with alkali metal alcoholate or alkali metal hydroxide at room temperature or near room temperature, and then reacting with soluble zinc salt.
As an improvement, the conjugated linoleic acid is a pure product of the conjugated linoleic acid or a mixed fatty acid of the conjugated linoleic acid.
As a refinement, the alkali metal is lithium, potassium or sodium; the alcohol solution is any one or any two or any three of methanol, ethanol, ethylene glycol, propanol, isopropanol, 1, 2-propylene glycol, 1, 3-propylene glycol and glycerol or a mixture of any two or any three of the above and water.
The soluble zinc salt is any one of zinc chloride, zinc bromide, zinc sulfate, zinc nitrate or zinc acetate, or a mixture of two or three of zinc chloride, zinc bromide, zinc sulfate, zinc nitrate or zinc acetate.
A preparation method of a conjugated zinc oleate preparation comprises the following operation steps:
(1) adding aqueous solution or alcoholic solution of alkali metal hydroxide or alkali metal alcoholate into conjugated linoleic acid with equivalent weight under the protection of inert gas at room temperature or near room temperature, and stirring for reaction for 1-6 hours to obtain alkali metal soap solution of conjugated linoleic acid;
(2) adding an equivalent amount of soluble zinc salt solution into the solution generated in the step (1), stirring until solid is separated out, clarifying a liquid part, carrying out centrifugal separation, and removing clear liquid to obtain crude conjugated linoleic acid zinc salt;
(3) washing the crude conjugated zinc linoleate with deionized water and low molecular alcohol or ether, and vacuum drying at 20-90 deg.c to obtain the conjugated zinc linoleate preparation.
As an improvement, the conjugated linoleic acid is a pure product of the conjugated linoleic acid or a mixed fatty acid of the conjugated linoleic acid.
As a refinement, the alkali metal is lithium, potassium or sodium; the alcohol solution is any one or any two or any three of methanol, ethanol, ethylene glycol, propanol, isopropanol, 1, 2-propylene glycol, 1, 3-propylene glycol and glycerol or a mixture of any two or any three of the above and water.
The improvement is that the soluble zinc salt is any one of zinc chloride, zinc bromide, zinc sulfate, zinc nitrate and zinc acetate, or a mixture of two or three of zinc chloride, zinc bromide, zinc sulfate, zinc nitrate and zinc acetate.
As an improvement, the content of the synthesized conjugated linoleic acid zinc is consistent with that of the conjugated linoleic acid in the raw material, and the other components are zinc salts of the rest fatty acids contained in the raw material.
As an improvement, the conjugated zinc linoleate is used as a functional additive of nutriments, a medicinal component and a precursor of a nano material.
Compared with the prior art, the invention has the advantages that: the reaction is uniform, the product purity is high, the product quality is stable, and the method is particularly suitable for the field of biotechnology with high requirements on the product quality.
Detailed Description
The content of calcium and magnesium in the conjugated linoleic acid composite preparation is measured by a plasma emission spectrometer Perkin-Elmer Optima 7300V ICP. The conjugated linoleic acid content in the conjugated linoleic acid compound preparation is determined by a liquid chromatograph Agilent InfinityLab LC/MSD. The conjugated linoleic acid is mixed fatty acid and comprises the following components in percentage by weight: the Conjugated Linoleic Acid (CLA) was 85.18%, and the other fatty acids (including linoleic acid, oleic acid, stearic acid, etc.) were 14.82%.
Example one
(1) Weighing 30g of conjugated linoleic acid in 450ml of distilled water at the room temperature of 25 ℃ under the protection of nitrogen, adding 45ml of 10 wt% sodium hydroxide solution under stirring, and stirring for 2 hours to obtain a conjugated sodium linoleate solution;
(2) adding 106ml of 10 wt% zinc chloride solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated zinc linoleate preparation;
(3) washing the crude preparation with distilled water, deionized water and methanol in sequence, vacuum drying at 60 ℃, and crushing to obtain 30.6g of a product.
Example two
(1) Weighing 30g of conjugated linoleic acid in 300ml of distilled water at the temperature of 30 ℃ near room temperature under the protection of nitrogen, adding 42ml of 10 wt% sodium hydroxide solution under stirring, and stirring for 4 hours to obtain a sodium solution of the conjugated linoleic acid;
(2) adding 160ml of 10 wt% zinc bromide solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated zinc linoleate preparation;
(3) washing the crude preparation with distilled water, deionized water and diethyl ether in sequence, vacuum drying at 50 ℃, and crushing to obtain 30.18g of a product.
EXAMPLE III
(1) Weighing 30g of conjugated linoleic acid in 300ml of methanol at the temperature of 35 ℃ near room temperature under the protection of nitrogen, adding 48ml of 10 wt% potassium hydroxide solution under stirring, and stirring for 4 hours to obtain a potassium solution of the conjugated linoleic acid;
(2) adding 180ml of 10 wt% zinc sulfate solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated zinc linoleate preparation;
(3) washing the crude preparation with distilled water, deionized water and methanol in sequence, vacuum drying at 80 ℃, and crushing to obtain 30.68g of a product.
Example four
(1) Weighing 30g of conjugated linoleic acid in 400ml of propanol at the temperature of 45 ℃ near room temperature under the protection of nitrogen, adding 45ml of 10 wt% potassium hydroxide solution under stirring, and stirring for 2.5 hours to obtain a potassium solution of the conjugated linoleic acid;
(2) adding 165ml of 10 wt% zinc sulfate solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated linoleic acid zinc preparation;
(3) washing the crude preparation with distilled water, deionized water and methanol in sequence, drying in vacuum at 60 ℃, and crushing to obtain 33.18g of a product.
EXAMPLE five
(1) Weighing 30g of conjugated linoleic acid in 408ml of propanol at the room temperature of 25 ℃ under the protection of argon, adding 31ml of 10 wt% potassium hydroxide solution under stirring, and stirring for 5 hours to obtain a potassium solution of the conjugated linoleic acid;
(2) adding 165ml of 10 wt% zinc sulfate solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated linoleic acid zinc preparation;
(3) washing the crude preparation with distilled water, deionized water and ethanol in sequence, drying in vacuum at 75 ℃, and crushing to obtain 30.81g of a product.
EXAMPLE six
(1) Weighing 30g of conjugated linoleic acid in 541ml of methanol at room temperature of 25 ℃ under the protection of argon, adding 33ml of 10 wt% potassium hydroxide solution under stirring, and stirring for 5 hours to obtain a potassium solution of the conjugated linoleic acid;
(2) adding 165ml of 10 wt% zinc chloride solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated linoleic acid zinc preparation;
(3) washing the crude preparation with distilled water, deionized water and ethanol in sequence, vacuum drying at 80 ℃, and crushing to obtain 32.18g of a product.
EXAMPLE seven
(1) Weighing 30g of conjugated linoleic acid in 540ml of methanol at the room temperature of 25 ℃ under the protection of argon, adding 48ml of 10 wt% potassium hydroxide solution under stirring, and stirring for 6 hours to obtain a potassium solution of the conjugated linoleic acid;
(2) adding 180ml of 10 wt% zinc chloride solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated linoleic acid zinc preparation;
(3) washing the crude preparation with distilled water, deionized water and methanol in sequence, drying in vacuum at 85 ℃, and crushing to obtain 33.86g of a product.
Example eight
(1) Weighing 30g of conjugated linoleic acid in 455ml of methanol at a temperature close to 36 ℃ under the protection of argon, adding 48ml of 10 wt% sodium hydroxide solution under stirring, and stirring for 5 hours to obtain a sodium solution of the conjugated linoleic acid;
(2) adding 153ml of 10 wt% zinc solution (the molar ratio of zinc chloride to zinc bromide is 1: 1) while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated linoleic acid zinc preparation;
(3) washing the crude preparation with distilled water, deionized water and propanol in sequence, vacuum drying at 65 ℃, and crushing to obtain 31.8g of a product.
Example nine
(1) 20g of conjugated linoleic acid is weighed in 255ml of alcoholic solution (methanol and ethanol) at the temperature of nearly 40 ℃ under the protection of nitrogen
The volume ratio of the alcohol is 2: 1) adding 24ml of 10 wt% sodium hydroxide solution while stirring, and stirring for 3 hours to obtain a sodium solution of conjugated linoleic acid;
(2) adding 90ml of 10 wt% ferrous chloride solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated linoleic acid zinc preparation;
(3) washing the crude preparation with distilled water, deionized water and diethyl ether in sequence, vacuum drying at 55 ℃, and crushing to obtain 16.8g of a product.
Example ten
(1) Weighing 20g of conjugated linoleic acid in 285ml of alcoholic solution (the volume ratio of methanol to water is 2: 1) at the temperature of 8 ℃ near room temperature under the protection of nitrogen, adding 30ml of 10 percent wt sodium hydroxide solution under stirring, and stirring for 6 hours to obtain sodium solution of the conjugated linoleic acid;
(2) adding 88ml of 10 wt% zinc chloride solution while stirring to form a light yellow granular substance, and performing centrifugal separation to obtain a crude conjugated zinc linoleate preparation;
(3) washing the crude preparation with distilled water, deionized water and ethanol in sequence, drying in vacuum at 25 ℃, and crushing to obtain 18.16g of a product.
TABLE 1 component content of the conjugated linoleic acid iron preparations prepared in the examples of the present invention
Figure BDA0002348349580000051
Figure BDA0002348349580000061

Claims (10)

1. The conjugated zinc linoleate preparation is characterized by being prepared from the following raw materials in molar ratio: conjugated linoleic acid: soluble zinc salt 2: 1.00-1.50;
the conjugated linoleic acid zinc preparation is prepared by the steps of firstly saponifying a pure product of conjugated linoleic acid with biological functional activity with alkali metal alcoholate or alkali metal hydroxide at room temperature or near room temperature, and then reacting with soluble zinc salt.
2. The preparation of claim 1, wherein the conjugated linoleic acid is a pure product of conjugated linoleic acid or a mixed fatty acid of conjugated linoleic acid.
3. The preparation of claim 1, wherein the alkali metal is lithium, potassium or sodium; the alcohol solution is any one or any two or any three of methanol, ethanol, ethylene glycol, propanol, isopropanol, 1, 2-propylene glycol, 1, 3-propylene glycol and glycerol or a mixture of any two or any three of the above and water.
4. The preparation of claim 1, wherein the soluble zinc salt is any one of zinc chloride, zinc bromide, zinc sulfate, zinc nitrate, and zinc acetate, or a mixture of two or three of zinc chloride, zinc bromide, zinc sulfate, zinc nitrate, and zinc acetate.
5. The preparation method of the conjugated zinc oleate preparation is characterized by comprising the following operation steps:
(1) adding aqueous solution or alcoholic solution of alkali metal hydroxide or alkali metal alcoholate into conjugated linoleic acid with equivalent weight under the protection of inert gas at room temperature or near room temperature, and stirring for reaction for 1-6 hours to obtain alkali metal soap solution of conjugated linoleic acid;
(2) adding an equivalent amount of soluble zinc salt solution into the solution generated in the step (1), stirring until solid is separated out, clarifying a liquid part, carrying out centrifugal separation, and removing clear liquid to obtain crude conjugated linoleic acid zinc salt;
(3) washing the crude conjugated zinc linoleate with deionized water and low molecular alcohol or ether, and vacuum drying at 20-90 deg.c to obtain the conjugated zinc linoleate preparation.
6. The method of claim 5, wherein the preparation of the conjugated zinc oleate is prepared by the following steps: the conjugated linoleic acid is a pure product of the conjugated linoleic acid or a mixed fatty acid of the conjugated linoleic acid.
7. The method of claim 5, wherein the preparation of the conjugated zinc oleate is prepared by the following steps: the alkali metal is lithium, potassium or sodium; the alcohol solution is any one or any two or any three of methanol, ethanol, ethylene glycol, propanol, isopropanol, 1, 2-propylene glycol, 1, 3-propylene glycol and glycerol or a mixture of any two or any three of the above and water.
8. The method of claim 5, wherein the preparation of the conjugated zinc oleate is prepared by the following steps: the soluble zinc salt is any one of zinc chloride or zinc bromide or zinc sulfate or zinc nitrate or zinc acetate, or a mixture of two or three of zinc chloride or zinc bromide or zinc sulfate or zinc nitrate or zinc acetate.
9. The method of claim 5, wherein the preparation of the conjugated zinc oleate is prepared by the following steps: the content of the synthesized conjugated linoleic acid zinc is consistent with that of the conjugated linoleic acid in the raw material, and the other components are zinc salts of the rest fatty acids in the raw material.
10. The method of claim 5, wherein the preparation of the conjugated zinc oleate is prepared by the following steps: the conjugated zinc linoleate is used as a functional additive of nutriments, a medicinal component and a precursor of a nano material.
CN201911404782.4A 2019-12-31 2019-12-31 Conjugated zinc linoleate preparation and preparation method thereof Pending CN110897165A (en)

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101849932A (en) * 2010-04-15 2010-10-06 广东海洋大学 Nutrient preparation of iron and zinc and preparation method thereof
CN101849962A (en) * 2010-04-15 2010-10-06 广东海洋大学 Lipid-lowering and weight-losing complex nutrient preparation and preparation method thereof
CN101849933A (en) * 2010-04-15 2010-10-06 广东海洋大学 Conjugated linoleic acid ferrite preparation and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101849932A (en) * 2010-04-15 2010-10-06 广东海洋大学 Nutrient preparation of iron and zinc and preparation method thereof
CN101849962A (en) * 2010-04-15 2010-10-06 广东海洋大学 Lipid-lowering and weight-losing complex nutrient preparation and preparation method thereof
CN101849933A (en) * 2010-04-15 2010-10-06 广东海洋大学 Conjugated linoleic acid ferrite preparation and preparation method thereof

Non-Patent Citations (1)

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Title
刘晓伟: "共轭亚油酸锌的合成工艺研究", 《天津化工》 *

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