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Chlorogenic acid

Pharmacological action Protecting liver, gallbladder The inhibitory effect on hyaluronidase and glucose - 6 - phosphatase The character of molecular structure Preparation method HPLC method for determination the content Toxicity Chemical property Uses Category Toxicity grading Acute toxicity Flammability hazard characteristics Storage and transport properties Fire extinguishing agent

CAS No.327-97-9
Chemical Name:Chlorogenic acid
Synonyms:Heriguard;NSC 70861;NSC 407296;Chlorogenic;Igasuric acid;Chlorogenic ac;HELIANTHIC ACID;CHLOROGENIC ACID;CAFFETANNIC ACID;CHLOROGENID ACID
CBNumber:CB2478906
Molecular Formula:C16H18O9
Formula Weight:354.31
MOL File:327-97-9.mol
Chlorogenic acid Property
Melting point : 210 °C (dec.)(lit.)
alpha : -36 º (c=1, H2O)
refractive index : -37 ° (C=1, H2O)
storage temp. : 0-6°C
Water Solubility : SOLUBLE IN HOT WATER
Merck : 2142
CAS DataBase Reference: 327-97-9(CAS DataBase Reference)
EPA Substance Registry System: Cyclohexanecarboxylic acid, 3-[[3-(3,4-dihydroxyphenyl)- 1-oxo-2-propenyl]oxy]-1,4, 5-trihydroxy-, (1S,3R,4R,5R)-(327-97-9)
Safety
Hazard Codes : Xi
Risk Statements : 68
Safety Statements : 24/25
WGK Germany : 3
RTECS : GU8480000
Hazard Note : Irritant

Chlorogenic acid Chemical Properties,Usage,Production

Pharmacological action
Chlorogenic acid is also called "green" auspicious acid, tannins "coffee", "coffee tannic acid", is a plant produce a styrene acrylic compounds through shikimic acid hitches in aerobic respiration process.It is coffee acyl quinic acid derivatives.The oxidation resistance is strong, and also has the anti HIV, anti tumor cells, antibacterial, improve central excited, cholagogue function.It has teratogenic, allergy and regulate the activity of cytochrome P450 ligase, and other functions.It is widely exist in more content honeysuckle plants. It is obtained by the water needle crystal, and it is the hemihydrate, when 110 ℃ it is to hydrate. Melting point is 208 ℃, [a] D25 33.5 ° (water, C = 1), K = 2.2 x 10-3 (27 ℃).It is weak acidity and convergence. When 25 ℃ , the solubility in water is 4%, easily soluble in hot water, but soluble in ethanol, acetone, slightly soluble in ethyl acetate, insoluble in chloroform, ether and carbon disulfide. It is azeotropic with concentrated hydrochloric acid and come to blue dye. It can make the bromine water fade, It is azeotropic with strong hydrogen iodide and obtain benzoic acid, It is obtained phenol by thermal decomposition together with water at 230 ℃, It decomposite to caffeic acid and quinic acid with dilute hydrochloric acid, and caffeic acid and quinic acid with dilute alkali at room temperature. Chlorogenic acid and its isomer different chlorogenic acid and green chlorogenic acid are in fruits of dicotyledonous plants, leaves, and other organizations,which is an important factor for plant metabolism. Chlorogenic acid has good biological activity, the transparent acid enzyme and inhibition of glucose - 6 - phosphatase, free radical lipid perxidation qing mutagenesis resistance and cardiovascular crown reinforcement, special efficacy in lipid-lowering, both anti-bacterial anti-virus, protecting liver cholagogic.
Chlorogenic acid as the condensation product of caffeic acid and quinic acid, is blue when meeting with iron, which is similar to tannins , but not precipitated with protein, so no convergence. Caffeic acid and chlorogenic acid has the wide bacteriostasis, but can be inactivated protein in the body. This product is similar to caffeine, oral or intraperitoneal injection, can improve the rat central excitability. Oral the drug of chlorogenic acid and coffee acid can increase the amount of hydrochloric acid secretion in the stomach, and can make slow pulse, and quinic acid is not. Chlorogenic acid could significantly increase small intestine peristalsis on the rat or mouse. Chlorogenic acid, caffeic acid and quinic acid can increase the tension of rat uterus, this function can be cancelled by papaverine, while atropine can't influence. Caffeic acid, chlorogenic acid, also can promote bile secretion in rats. On the specimens of rabbit ileum in vitro, this product can enhance the effect of adrenaline, but has no effect on blood glucose of adrenaline.
Protecting liver, gallbladder
Chlorogenic acid in flos lonicerae has favorable gallbladder function, promoting biliary Secretion of rats. Injection of 200 mg/kg chlorogenic acid to browns MAO honeysuckle total saponins subcutaneous can be significantly against CCl4, paracetamol and the increase of serum GPT caused by galactosamine in mice liver and liver triglyceride levels, and significantly reduce the severity of the liver pathological damage, making dot necrosis number sum and necrosis occur rate liver decreased obviously.
The inhibitory effect on hyaluronidase and glucose - 6 - phosphatase
Hyaluronic cranberry (HAase) is one of the cracking mucopolysaccharide enzymes, can catalyze hyaluronic acid (HA) decomposition,which is in relation to the permeability of vascular system and inflammation. HA is a mucopolysaccharide, which is composed of uronic acid and acetyl glucosamine, having a variety of functions, such as heal, make the skin wetting health, lubricating joints and prevent inflammation, etc. 3, 5-2 coffee acyl quinic acid (artichoke acid) and chlorogenic acid found in the ethyl acetate extract from the narrow assists cone flower (Echinacea amgustifolia DC) roots have stronger inhibitory effect of HAase activated. Animal in vitro studies have demonstrated that chlorogenic acid can not reversible inhibition of glucose - 6 - hydrolysis of phosphatase, reduce liver glycogen decomposition and exogenous glucose absorption. Animal studies have shown that the use of chlorogenic acid can reduce high blood sugar spikes caused by the use of glucagon (glycogenolysis). Therefore, chlorogenic acid can lower blood sugar level, improve the liver glucose - 6 - phosphoric acid and the concentration of hepatic glycogen.
The character of molecular structure
Chlorogenic acid is formed by caffeic acid and quinic acid, and the molecular structure has ester bond, unsaturated double bond and polyphenol unstable part of the three. In the process of extracted from plants, chlorogenic acid often happen by hydrolysis and intramolecular ester base migration isomerization . Due to the special structure of chlorogenic acid, it can extract from plants by the polarity solvent such as ethanol, acetone, methanol. But due to the instability of chlorogenic acid itself, extraction can not be in high temperature, strong light and heat for a long time. Chlorogenic acid liquid were placed in brown bottle, refrigerator (2 ℃) to save to be the most stable.
Preparation method
It can be obtained by (1S)-1- ethoxyformyloxy-3-cis-[3,4-dihydroxy-anti-cinnamoyl oxygen radicals] - 4'- anti-5'- anti-dihydroxy cyclohexane -γ-methyl formate with barium hydroxide in methanol catalytic hydrolysis, or by the segregation from green coffee beans.
HPLC method for determination the content
(1)Chromatographic conditions: octadecyl silane bonded silica gel as the filling agent; Acetonitrile -0.4% phosphoric acid solution (13:87) as mobile phase; Detection wavelength of 327 nm. Theoretical plate number according to the chromatographic peak of chlorogenic acid is greater than 1000. (2)the preparation of the reference substance solution: precisely weigh the right amount of chlorogenic acid reference substance, placed in brown volumetric flask, adding 50% methanol solution containing 40 μg /mL (saving below 10 ℃). (3)the preparation of sample solution: taking samples of dry powder is about 0.5 g, precision said, with a plug in the conical flask, adding 50 ml 50% methanol , 30 min ultrasonic processing , cooling, weighing, make up the weight loss reduction with 50% methanol, shake well, filtration, abandoned the early filtrate, precision measuring duration of filtrate 5 ml, 25 ml volumetric brown flask , add 50% methanol to the scale, shake well. (4)assimilate precision respectively from each 10 μL reference substance and the sample solution, injection liquid chromatograph, determination,obtained.
Toxicity
Chlorogenic acid is sensitive to people, can cause asthma, dermatitis, but no this reaction to the oral of chlorogenic acid. It can be active no sensitization substances by small intestinal secretions convertion to. The toxicity of chlorogenic acid is very small, LD50 is greater than 1 g/kg to young rats, intraperitoneal injection of greater than 0.25 g/kg.
Chemical property
Hemihydrate is needle crystal (water). When 110 ℃, it become to anhydrous compounds. Melting point: 208 ℃, [alpha] 20D- 35.2 (C = 2.8). When 25 ℃, water solubility was 4%, solubility is bigger in the hot water. Soluble in ethanol and acetone, slightly soluble in ethyl acetate.
Uses
It has broad antibacterial effect, advantageous bravery, hemostatic, increase white blood cell and antiviral effect, the effect of the blood clotting and bleeding time is shortened. It is used in the treatment of upper respiratory tract infection, anti-inflammatory and antipyretic, cool blood heat dissipation. Used as pharmaceutical raw materials and intermediates. clearing heat and removing toxicity, cold wind heat, broad-spectrum antimicrobial properties, having obvious inhibitory effect to hemolytic streptococcus, dysentery rod gas and salmonella typhi bacteria
Category
Toxic substances
Toxicity grading
toxication
Acute toxicity
Abdominal cavity - rat LDL0:4000 mg/kg
Flammability hazard characteristics
Combustible; Release acrid smoke fire
Storage and transport properties
Low temperature warehouse, ventilated, dry
Fire extinguishing agent
Water, carbon dioxide, dry powder, sand
Chemical Properties
white to slightly yellowish-beige powder
Usage
antioxidant, free radical scavenger
Usage
A major component of green coffee the extracts of which promote weight loss in overweight and obese people. Chlorogenic Acid is an important intermediate in lignin biosynthesis. Chlorogenic Acid is an antioxidant and an inhibitor of the tumor promoting activity of phorbol ester. It has protective effect against streptozotocin-nicotinamide generated oxidative stress induced diabetes and may also pr otect against cardiovascular disease.
Chlorogenic acid Preparation Products And Raw materials
Raw materials
Preparation Products
Chlorogenic acid Suppliers      Global( 326)Suppliers     
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Shanghai Boyle Chemical Co., Ltd. Mr Qiu:021-50182298(Demestic market) Miss Xu:021-50180596(Abroad market)+86-21-57758967sales@boylechem.comCHINA 2221 55
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Meryer (Shanghai) Chemical Technology Co., Ltd. +86-(0)21-61259100(Shanghai) +86-(0)755-86170099(ShenZhen) +86-(0)10-59487313(Beijing)+86-(0)21-61259102(Shanghai) +86-(0)755-86170066(ShenZhen) +86-(0)10-88580358(Beijing)sh@meryer.comCHINA 40406 62
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CHLOROGENIC ACID, TRANS CHLOROGENIC ACID HELIANTHIC ACID ISOCHLOROGENIC ACID CAFFEOLYQUINIC ACID CAFFEOYLQUINIC ACID CAFFETANNIC ACID CAFFEYLQUINIC ACID (1s,3r,4r,5r)-3-[[3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-1,4,5-trihydroxycyclohexanecarboxylic acid 327-97-9 3-[[3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENYL]OXY] 1,4,5-TRIHYDROXYCYCLOHEXANECARBOXYLIC ACID 3-(3,4-DIHYDROXYCINNAMOYL)-D(-)-QUINIC ACID 3-(3,4-DIHYDROXYCINNAMOYL)QUINIC ACID 1,3,4,5-TETRAHYDROXY-CYCLOHEXANECARBOXYLIC ACID 3-[3,4-DIHYDROXYCINNAMATE] BioChemical Antioxidant and Free Radical Scavengers Cancer Research Chemopreventive Agents 5-O-(3,4-Dihydroxycinnamoyl)-L-quinic acid 5-(3,4-DIHYDROXYCINNAMOYL)-D-(-)-QUINIC ACID 3R-[[3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENYL]OXYL]-1S,4R,5R-TRIHYROXY-CYCLOHEXANECARBOXYLIC ACID 3-O-(3,4-DIHYDROXYCINNAMOYL)-D-QUINIC ACID 3-O-CAFFEOYLQUINIC ACID 3-CAFFEOYLQUINIC ACID NSC 407296 3-((3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-cyclohexanecarboxylicaci 3-[3-C[3-(3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENY1]OXY]1,4,5-TRIHYDROXY-,[1S-(1α,3β,4α,5α)]- 5-trihydroxy-,(1s-(1-alpha,3-beta,4-alpha,5-alpha))-4 CYCOLOHEXANECABOXYLIOACID CHLOROGENIC ACIDS chlorogenic acid (natural) CHLOROGENIC ACID PLANT CELLCULTURE TESTE D CHLOROGENIC ACID CRYSTALLINE CHLOROGENIC ACID, PREDOMINANTLY TRANS ChlorogenicAcid(EucommiaUlmoidesOliverPe)20%ByHplc 327-97-7 C16H18O9 Chlorogenic acid, predominantly trans, from coffee seeds, 99% Chlorogenic Cyclohexanecarboxylic acid, 3-3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyloxy-1,4,5-trihydroxy-, (1S,3R,4R,5R)- (1R,3R,4S,5R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxy-cyclohexane-1-carboxylic acid CHLOROGENID ACID CHLOROGENIC ACID(AHP) 3-CAFFEOLYQUINICACID 3-[[3-(3,4-dihydroxyphenyl)-1-oxy-2-propenyl]oxy]-1,4,5-trihydroxy-1, [1S-(1 a , 3 β , 4 a , 5 a )] Plant Oils, Toxins, Phenolic Acids & Derivatives (1S,3R,4R,5R)-3-[[3-(3,4-Dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-1,4,5-trihydroxycyclohexanecarboxylic acid Chlorogenic Acid Hydrate C16H18O9xH2O Natural Plant Extract The group of Chlorogenic acid CHLOROGENIC ACID extrapure Chlorogenic acid,3-Caffeoylquinic acid Cyclohexanecarboxylic acid, 3-((3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl)oxy)- 1,4,5-trihydroxy-, (1S-(1-alpha,3-beta,4-alpha,5-alpha)) Heriguard Chlorogenic acid, 99%, predominantly trans, from coffee seeds [1S,4R,5R,(-)]-3β-[[3-(3,4-Dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-1,4,5-trihydroxycyclohexanecarboxylic acid 1,4α,5α-Trihydroxy-3β-[3-(3,4-dihydroxyphenyl)acryloyloxy]cyclohexane-1β-carboxylic acid
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