CN1445212A - Microwave once process for extracting capsaicin and pigment - Google Patents

Microwave once process for extracting capsaicin and pigment Download PDF

Info

Publication number
CN1445212A
CN1445212A CN02131467A CN02131467A CN1445212A CN 1445212 A CN1445212 A CN 1445212A CN 02131467 A CN02131467 A CN 02131467A CN 02131467 A CN02131467 A CN 02131467A CN 1445212 A CN1445212 A CN 1445212A
Authority
CN
China
Prior art keywords
pigment
acid
capsaicine
extracting
acetone
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN02131467A
Other languages
Chinese (zh)
Other versions
CN1186314C (en
Inventor
谢渭利
陈丹云
高景曦
李�杰
张春
吉欣
仇波
Original Assignee
高景曦
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 高景曦 filed Critical 高景曦
Priority to CNB021314675A priority Critical patent/CN1186314C/en
Publication of CN1445212A publication Critical patent/CN1445212A/en
Application granted granted Critical
Publication of CN1186314C publication Critical patent/CN1186314C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Landscapes

  • Medicines Containing Plant Substances (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

A microwave process for extracting capsaicin and pigment from chili includes such steps as extracting capsaicin in alkali solution by microwave radiation, separating and purifying by polar microreticular resin column, and extracting pigment from dregs by acetone or alcohol. Its advantages are very short time for extruting and low cost and environmental protection process.

Description

Extraction method of the microwave of capsaicine and pigment
The present invention relates to a kind of natural active matter leaching method, particularly in ripe capsicum, obtain the method for capsaicine and food dye continuously with the microwave buck.
Existing technical literature such as Chinese patent " extract the novel process of capsanthin and capsaicine in red pepper " and " extracting method of capsochrome and capsaicine " and document " screening of capsaicine extracting method " northwest pharmaceutical journal 1996.11 (2) is used all is first with ethanol or acetone and other organic solvent extracting.Find all that in our simulation test the aftertreatment separation circuit is complicated and be difficult for dividing clean.The present invention has improved the first step extracting, utilizes capsaicine to dissolve in the buck and the water insoluble character of pigment, at first with containing NaOH or the KOH buck proposes peppery element.Separation is with look fully and not, is placed in the microwave field when extracting and handles, and extracting has speeded up tens times.Filtering bits are obtained pigment by the known technology of literature method again.Isolating capsicum is young takes out or material such as processing oils, not in this patent scope.
Capsaicine has another name called capsicine, illustrious name (Capsaicin).It is the main composition that produces pungent in the capsicum.Its molecular structure is one and holds dimethyl nine carbochain methoxyl groups to phenol that the 8th a last amide group is a kind of plant acid amides.65 ℃ of fusing points dissolve in organic solvent and the buck.Modern studies show that it has of great value physiologically active.Strong and persistent anti-inflammatory analgesic action is arranged, and making dressing has significant curative effect to chronic rheumatic arthritis, zoster, neurodynia, and psoriasis, baldness are also had therapeutic action, and is again the major ingredient of making the tearing property defensive weapon.Present in the world price per kilogram is more than 5,000 dollars.This just has exploitation to be worth very much.
Another kind of material in the capsicum is natural food colour Capsorubin and Capsanthin (Cap-sorubin and Capsanthin), and the both is the oil soluble toxicological harmless pigment of multiple ketene.Domestic have quite a lot of manufacturer production, and its valency also can reach one kilogram in thousands of units.But mostly capsaicine is carried as refuse or byproduct based on the factory that produces pigment in many producers, the low and quality of yield can not reach export standard.This also be we to study improve technology, to obtain the invention reason of bigger comprehensive benefit.
Our comprehensive extractive processing method be earlier the drying and ripening red pepper of choosing is broken in rotating knife formula beating crusher<fragment of 3mm, filter out young grain do in addition other composition exploitation with or sell.Again that fragmentation is good capsicum is packed in the Glass Containers.Adding the NaOH of 0.2~1.8Mol or KOH solution soaking is placed on after saturating and accepts microwave radiation in the microwave radiation field and handle.System total mass and microwave energy have been calculated with 0.5~5 watt/milliliter Power Processing.Investigating method heats up system temperature with the control temperature rise and is not more than 50 ℃, after disposing solution is filtered, filtrate is used for further extracting capsaicine, and filter residue continues processing and extracts pigment, boils off solvent and promptly can be used as the sale of commodity capsochrome with conventional organic solvent (ethyl acetate, the sixth of the twelve Earthly Branches alkane, acetone, ethanol etc.).
Solution after more than filtering is earlier with acid (Hcl, H 2SO 4, HCOOH and acetic acid) transfer between PH11~8, (concrete model is XAD-7, NKA-9 by polar macroporous adsorption resin then, D145, D160, S-8, NKA-II, HPD-800 etc.) post fully is adsorbed on the resin capsaicine, goes up new post when pungent appears in effluent liquid again.Treating that the saturated back of post absorption capsaicine is cleaned behind the post with organic solvent such as ethyl acetate, ethanol, benzene, hexane, ether, acetone, trichloromethane etc. with pure water gives wash-out.Again elutriant is reduced pressure to steam and stay, promptly get purer capsaicine except that after desolvating.As also not reaching requirement, again product is dissolved in ethanol or the acetone, filter and get elaboration with activated carbon decolorizing, recrystallize.
Present method buck be it seems the more of usefulness, but the buck that gets off from adsorption column, and available strong basic ion exchange resin is removed acid group, can continue again to use after adjusting PH>12, and this has just greatly alleviated the environmental pollution of buck.The subsequent technique organic solvent will reclaim again, sees that thus processing method of the present invention also is comparatively favourable and feasible to the protection environment.
We set up testing method earlier before doing test, and we are according to the Sodium Nitrite on the classical documents---the Sodium orthomolybdate colorimetry.At the 420nm wavelength measurement, typical curve A=2.880m (mg)+0.0076, r=0.999.Test capsaicin content: % in the different location chilli of buying behind the establishment method respectively
Nanyang, Sichuan, Zhecheng, Henan
0.55 1.39 0.87
Getting Nanyang produces red pepper and is placed in the cutter formula rotation powder beating device and smashes to 3mm.About 260 grams that get screen out the capsicum son, and are standby.
Preparation 2%NaOH solution (about 0.5Mol) is got 400ml and is placed in the 500ml Florence flask, claim 25 gram be above-mentioned to go young red chilly powder to put into, soaking and stirring is not placed on and opens in the microwave oven on the 500W shelves to there being bubble, about three minutes of time, cold filtration is put in taking-up, collection filtrate is put into another 500 milliliters of Erlenmeyer flasks, filter residue adds a little 0.5MolNaOH again and soaks, and is merged filtrate after the filtration, transfers PH to 11 lower slightly with Hcl.Last two φ 2cm * 20cm resin columns, a dress NKA-9 (Nankai University's product) adorns commercially available XAD-7 for one and divides two halves to drip upper prop the above-mentioned alkali lye that contains capsaicine.Adding back observation effluent liquid has not had pungent, and each crosses post with the cold aquae destillata of 50ml again.Use 95% ethanol after washing instead and dripped the post desorb, merge two groups of elutriants and be placed on and heat in the rotatory evaporator about 45 ℃, open off-gas pump to ethanol and steam in a large number.Until do, take off the eggplant bottle, the capsaicine, the color that are bonded on bottle wall with the careful scraping of little spoon are white or little Huang.On analytical balance, weigh 149mg, calculated yield is 67%.
The above capsaicine that obtains recrystallization in a large amount of ethyl acetate is obtained thin platelike crystal, the oven dry of finding time in vacuum drier.Taking away to record on ultraviolet scanner at 210 millimicrons has small one and large one absorption peak with the 254nm place, with the literature value basically identical.Get some again and recording infrared light praseodymium absorption peak on the IR-FT instrument: methoxyl group on the 2890 and 1455 corresponding phenyl ring, 1651cm with pellet technique -1Corresponding secondary amide base, 1274 corresponding to aryl ethers, and 1381 corresponding to the end sec.-propyl, and 1419 corresponding to methylene radical ketone, and 2930 corresponding to alkane.What confirm that we obtain with this is capsaicine.(referring to accompanying drawing)
Illustrate by other two embodiment more below:
Example one:
Get Zhecheng, commercially available Henan and produce chilli 300 grams, smash the son.Claim 25 gram green pepper powder to be positioned in the 500ml flask, 400 milliliters of NaOH solution that add 0.25Mol (about 1%), be dipped into and stir no bubble, be placed in the microwave oven with 500 watts of power in addition the width of cloth according to 160 seconds, put cold after-filtration, filter residue add again 100ml0.5MolKOH once more in microwave oven with the power width of cloth according to 100 seconds, cold filtration, merge filtrate twice, add acetic acid and transfer PH to 11, last AB-8 resin column absorption, back 95% ethanol elution, on rotatory evaporator, extremely do with 250ml pyriform flask reduction vaporization, scrape product, weigh 98.3mg, calculated yield ≈ 72%.
Example two:
Get high-load Sichuan capsicum and beat powder and go the son, get 25 grams, method is done on the photograph.Leach liquor is used 1.2Mol KOH instead, and secondary leaches the 1.8Mol NaOH with the same amount, D160 resin column absorption on the merging filtrate.Use eluent ethyl acetate, on rotatory evaporator, be decompressed to 45 ℃ of boilings, evaporate to dryness in 250ml pears type bottle, scrape get the product capsaicine weigh 265mg, calculated yield gets 76.2%.
Reach two examples in sum, its yield total all about in the of 70%, trace it to its cause.We think that one is because container is little, each output several grams of a zero point, be difficult to receive clean, and product to spread area out big, be skim, the part of can volatilizing; Two come our experimental technique that the imperfection place is still arranged, as the macroporous adsorbent resin pre-treatment of purchasing is not ideal enough.All can influence yield.Guess and amplify pilot scale on several hectograms during kilogram, yield also can improve.
With regard to the estimation of present yield, the per kilogram product needs the raw material capsicum at 100~250Kg, and with the matter of fundamental importance, the per kilogram product cost valencys such as solvent loss, depreciation that add are also below 20,000 yuan.That is to say that take out with 5,000 dollars of/kilogram calculations, rate of gross profit is greater than 50%.In addition the pigment product that reclaims has been close to net profit.Therefore this technology has market potential.

Claims (4)

1. method of in red pepper, extracting capsaicine and pigment, it is characterized in that earlier capsicum being pulverized, add a certain amount of alkali lye, soak and to be placed on evenly that the power width of cloth with 0.5~5 watt of every liter of system shines in the microwave radiation field, after-filtration is handled in control temperature rise ≯ 50 ℃, and filtrate is gone up polar macroporous resin column and separated behind the acid adjustment degree, use the organic solvent wash-out again, elutriant evaporated under reduced pressure solvent obtains capsaicine; Filter residue is used acetone, hexane or extraction using alcohol again, boils off solvent and gets pigment.
2. quantitative alkali lye as claimed in claim 1 refers to NaOH or the KOH with 5~25 times 0.2~1.8 volumetric molar concentration of red chilly powder weight.
3. the acid that acid adjustment degree as claimed in claim 1 is used is hydrochloric acid, sulfuric acid formic acid and acetate, and pH value is adjusted to 8~11.
4. the wash-out organic solvent described in claim 1 is ethyl acetate, ethanol, benzene, ether and trichloromethane and acetone.
CNB021314675A 2002-10-16 2002-10-16 Microwave once process for extracting capsaicin and pigment Expired - Fee Related CN1186314C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB021314675A CN1186314C (en) 2002-10-16 2002-10-16 Microwave once process for extracting capsaicin and pigment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB021314675A CN1186314C (en) 2002-10-16 2002-10-16 Microwave once process for extracting capsaicin and pigment

Publications (2)

Publication Number Publication Date
CN1445212A true CN1445212A (en) 2003-10-01
CN1186314C CN1186314C (en) 2005-01-26

Family

ID=27811326

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB021314675A Expired - Fee Related CN1186314C (en) 2002-10-16 2002-10-16 Microwave once process for extracting capsaicin and pigment

Country Status (1)

Country Link
CN (1) CN1186314C (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102058083A (en) * 2010-11-09 2011-05-18 老河口华松科技有限责任公司 Method for preparing water-soluble chili fine powder by chili skin
CN102127448A (en) * 2010-12-22 2011-07-20 晨光生物科技集团股份有限公司 Method for extracting oxidation-resistant substance from capsicum residues
CN102516802A (en) * 2011-12-12 2012-06-27 山东凯斯达机械制造有限公司 Method for extracting capsicum red pigment and capsaicin
CN103798133A (en) * 2014-01-23 2014-05-21 青岛农业大学 Method for breeding hot pepper stable inheritance selfining line with high haematochrome content and difficult to fade
CN104003897A (en) * 2014-06-19 2014-08-27 南京麦思德餐饮管理有限公司 Method for preparing capsaicin
CN106752072A (en) * 2016-12-05 2017-05-31 晨光生物科技集团股份有限公司 A kind of High color values capsanthin continuous production processes
CN106966917A (en) * 2017-03-08 2017-07-21 黄冈师范学院 Extraction separation method, capsorubin, the capsaicine of raw material of hot pepper

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102058083A (en) * 2010-11-09 2011-05-18 老河口华松科技有限责任公司 Method for preparing water-soluble chili fine powder by chili skin
CN102058083B (en) * 2010-11-09 2012-12-19 老河口华松科技有限责任公司 Method for preparing water-soluble chili fine powder by chili skin
CN102127448A (en) * 2010-12-22 2011-07-20 晨光生物科技集团股份有限公司 Method for extracting oxidation-resistant substance from capsicum residues
CN102127448B (en) * 2010-12-22 2013-04-24 晨光生物科技集团股份有限公司 Method for extracting oxidation-resistant substance from capsicum residues
CN102516802A (en) * 2011-12-12 2012-06-27 山东凯斯达机械制造有限公司 Method for extracting capsicum red pigment and capsaicin
CN103798133A (en) * 2014-01-23 2014-05-21 青岛农业大学 Method for breeding hot pepper stable inheritance selfining line with high haematochrome content and difficult to fade
CN103798133B (en) * 2014-01-23 2016-03-09 青岛农业大学 High and the selection of capsicum genetic stability inbred line not easy to fade of a kind of haematochrome content
CN104003897A (en) * 2014-06-19 2014-08-27 南京麦思德餐饮管理有限公司 Method for preparing capsaicin
CN106752072A (en) * 2016-12-05 2017-05-31 晨光生物科技集团股份有限公司 A kind of High color values capsanthin continuous production processes
CN106752072B (en) * 2016-12-05 2019-03-19 晨光生物科技集团股份有限公司 A kind of High color values capsanthin continuous production processes
CN106966917A (en) * 2017-03-08 2017-07-21 黄冈师范学院 Extraction separation method, capsorubin, the capsaicine of raw material of hot pepper

Also Published As

Publication number Publication date
CN1186314C (en) 2005-01-26

Similar Documents

Publication Publication Date Title
CN105802738B (en) Extraction method of wild chrysanthemum flower volatile oil
CN101200480A (en) Rebaudioside A and extraction method thereof
CN106008442A (en) Method for extracting anthocyanin from nitraria tangutorum peel residues
CN109609276A (en) A kind of extracting method of oil camphor tree leaf essential oil
CN102617468A (en) Method for ultrasound-assisted extraction of lappaconitine
CN102690208A (en) Method for extracting hydroxyl sanshool from zanthoxylum oil
CN109053821B (en) Method for extracting tea polyphenol, total amino acids and flavone compounds from momordica grosvenori leaves
CN104173438A (en) Preparation method of general flavone of purple perilla
CN110317126A (en) A kind of method and system for extracting cannabidiol in industrial hemp with microwave-assisted Subcritical Water Extraction technology
CN1186314C (en) Microwave once process for extracting capsaicin and pigment
CN102219814A (en) Method for extracting aucubin from eucommia ulmoides oliver seed draff
CN113754518A (en) Method for efficiently purifying cannabidiol from industrial cannabis sativa leaves
CN101289473A (en) Process for abstracting theasaponine by microwave/light wave dry method
CN111116323A (en) Microwave-assisted subcritical technology for extracting cannabidiol and preparation method thereof
CN107721967A (en) A kind of green-tea extract production technology of high EGCG content
CN102146143B (en) Method for preparing pectin and cellulose from extracting residues of ginseng and American ginseng and application thereof
CN113686990A (en) Method for extracting hesperidin from citrus to prepare hesperetin
CN109320576A (en) A kind of production method of high-content momordica grosvenori glycoside V
CN103083939B (en) Method for extracting borneol camphor tree leaf crude extract and applied response surface methodology
CN110330537B (en) Process for extracting high-purity crocin from gardenia fruit
CN113512020B (en) Method for extracting catechin and epicatechin from pericarp of plant of Camellia
CN109293728A (en) A kind of green low cost preparation method of high-purity tea saponin
CN102942455A (en) Method for extracting oxyresveratrol from mulberry branches
CN113082124A (en) Method for simultaneously preparing vitex rotundifolia seed oil and flavone extract
CN113200911A (en) Quinoline alkaloid compound and preparation method and application thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C57 Notification of unclear or unknown address
DD01 Delivery of document by public notice

Addressee: Gao Jingxi

Document name: Notification of Termination of Patent Right

C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20050126