CN105687117A - Method for producing lauryl sorbitan polyoxyethylene ether iodine complex gel - Google Patents

Method for producing lauryl sorbitan polyoxyethylene ether iodine complex gel Download PDF

Info

Publication number
CN105687117A
CN105687117A CN201410689383.8A CN201410689383A CN105687117A CN 105687117 A CN105687117 A CN 105687117A CN 201410689383 A CN201410689383 A CN 201410689383A CN 105687117 A CN105687117 A CN 105687117A
Authority
CN
China
Prior art keywords
lauryl sorbitan
polyoxyethylene ether
iodine complex
iodo
complexes
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.)
Pending
Application number
CN201410689383.8A
Other languages
Chinese (zh)
Inventor
唐青
冀红珍
唐铖
孙有光
高桂新
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TIANJIN BOKENI TECHNOLOGY DEVELOPMENT Co Ltd
Original Assignee
TIANJIN BOKENI TECHNOLOGY DEVELOPMENT Co Ltd
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 TIANJIN BOKENI TECHNOLOGY DEVELOPMENT Co Ltd filed Critical TIANJIN BOKENI TECHNOLOGY DEVELOPMENT Co Ltd
Priority to CN201410689383.8A priority Critical patent/CN105687117A/en
Publication of CN105687117A publication Critical patent/CN105687117A/en
Pending legal-status Critical Current

Links

Abstract

The present invention discloses a method for producing a lauryl sorbitan polyoxyethylene ether iodine complex gel, and the lauryl sorbitan polyoxyethylene ether iodine complex gel comprises a polyglycerol fatty acid ester iodine complex (with 10% of effective iodine), an acidifying agent, a polymer thickener and purified water. The lauryl sorbitan polyoxyethylene ether iodine complex gel is a deep purple gel in appearance, pH value is 4 to 6, and the iodine content is 0.3-0.5%.

Description

A kind of manufacture method of lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes gelinite
[technical field]
The present invention is the manufacture method of a kind of lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes gelinite。
[background technology]
Dermatophytes, fungal infection initiation dermatosis are the things that people are very painful, and some funguses, mycete are presented in human body naturally, when they touch a favourable environment, will at people's tumor growth, and the top layer of skin infection, fingernail and hair;Different fungus, fungal infection skin type have the tinea manuum, tinea pedis, tinea cruris, fingernail tinea, beard ringworm, tinea capitis。In rare cases, fungus, mycete undue growth, also result in infection to blood or internal;Human body also can be shown the diseases such as neural and endocrine regulation, immunosuppressant, carcinogenic teratogenesis, lesions of liver and kidney and breeding difficulty by mycotoxin。Mycete, fungus cause human genitals disease, common are the disease such as vaginitis, acrobystitis, and these diseases also bring very big misery;Burn, wound people's daily life common disease especially, it is the main problem needing to solve that the preventing of these diseases is infected;The problems referred to above are had and solve effect well by the present invention。
[summary of the invention]
The present invention its consist of lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine), acidulant, macromolecule thickener and pure water。
The present invention is made up of lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 2-6%, acidulant 0.2-0.5%, macromolecule thickener 0.5-3% and pure water 90-98%。
Acidulant of the present invention uses category to be citric acid, oxalic acid, tartaric acid etc.。
Macromolecule thickener of the present invention uses category to be methylcellulose, hydroxyethylmethyl-cellulose, carboxymethyl cellulose, ethyl cellulose, benzylcellulose, hydroxyethyl cellulose, hydroxypropyl methyl cellulose, carboxymethyl hydroxyethyl cellulose and benzyl cellulose etc.。
The present invention, with, in temperature controlled hermetic type stainless steel cauldron, adding pure water, is warming up to 40-50 DEG C and adds acidulant;Stirring;Add macromolecule thickener, after stirring 3-5 hour, carry out homogenizing with homogenizer, after homogenizing, in stirring simultaneously, be slowly added to lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine), stir 30 minutes;Temperature is down to 35 ± 2 DEG C of dischargings。Finished product need to be placed in lucifuge, nonmetallic container。
The dark purple thick shape mastic of outward appearance body shape of the present invention, is dissolved in water, and pH value is 4-6, content of iodine 0.3-0.5%。
The present invention manufacture raw material be easy to get, pollution-free in production process, without garbage, the requirement meeting environmental protective chemical industry production technology。
[detailed description of the invention]
Present invention composition includes: lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 2-6%, acidulant 0.2-0.5%, macromolecule thickener 0.5-3% and pure water 90-98% composition。
Manufacturing process route: with, in temperature controlled hermetic type stainless steel cauldron, adding pure water, be warming up to 40-50 DEG C and add acidulant;Stirring;Add macromolecule thickener, after stirring 3-5 hour, carry out homogenizing with homogenizer, after homogenizing, in stirring simultaneously, be slowly added to lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine), stir 30 minutes;Temperature is down to 35 ± 2 DEG C of dischargings。Finished product need to be placed in lucifuge, nonmetallic container。
Specific embodiment one:
By following part by weight throwing raw materials: lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 2 parts, citric acid 0.2 part, macromolecule thickener 1 part and pure water 96.8 parts。
Manufacturing process route: with, in temperature controlled hermetic type stainless steel cauldron, adding pure water 96.8 kilograms, be warming up to 40-50 DEG C and add citric acid 0.2 kilogram;Stirring;Add macromolecule thickener 1 kilogram, after stirring 3-5 hour, carry out homogenizing with homogenizer, after homogenizing, in stirring simultaneously, be slowly added to lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 2 kilograms, stir 30 minutes;Temperature is down to 35 ± 2 DEG C of dischargings。Finished product need to be placed in lucifuge, nonmetallic container。
Specific embodiment two:
By following part by weight throwing raw materials: lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 3 parts, citric acid 0.2 part, macromolecule thickener 1 part and pure water 95.8 parts。
Manufacturing process route: with, in temperature controlled hermetic type stainless steel cauldron, adding pure water 95.8 kilograms, be warming up to 40-50 DEG C and add citric acid 0.2 kilogram;Stirring;Add macromolecule thickener 2 kilograms, after stirring 3-5 hour, carry out homogenizing with homogenizer, after homogenizing, in stirring simultaneously, be slowly added to lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 3 kilograms, stir 30 minutes;Temperature is down to 35 ± 2 DEG C of dischargings。Finished product need to be placed in lucifuge, nonmetallic container。
Specific embodiment three:
By following part by weight throwing raw materials: lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 4 parts, citric acid 0.3 part, macromolecule thickener 2 parts and pure water 93.7 parts。
Manufacturing process route: with, in temperature controlled hermetic type stainless steel cauldron, adding pure water 93.7 kilograms, be warming up to 40-50 DEG C and add citric acid 0.3 kilogram;Stirring;Add macromolecule thickener 2 kilograms, after stirring 3-5 hour, carry out homogenizing with homogenizer, after homogenizing, in stirring simultaneously, be slowly added to lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 4 kilograms, stir 30 minutes;Temperature is down to 35 ± 2 DEG C of dischargings。Finished product need to be placed in lucifuge, nonmetallic container。

Claims (2)

1. the manufacture method of a lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes gelinite, it is characterised in that: consist of lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine), acidulant, macromolecule thickener and pure water。
2. the manufacture method of a kind of lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes gelinite according to claim 1, it is characterised in that: consist of lauryl Sorbitan polyoxyethylenated alcohol iodo-complexes (10% available iodine) 2-6%, acidulant 0.2-0.5%, macromolecule thickener 0.5-3% and pure water 90-98%。
CN201410689383.8A 2014-11-26 2014-11-26 Method for producing lauryl sorbitan polyoxyethylene ether iodine complex gel Pending CN105687117A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410689383.8A CN105687117A (en) 2014-11-26 2014-11-26 Method for producing lauryl sorbitan polyoxyethylene ether iodine complex gel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410689383.8A CN105687117A (en) 2014-11-26 2014-11-26 Method for producing lauryl sorbitan polyoxyethylene ether iodine complex gel

Publications (1)

Publication Number Publication Date
CN105687117A true CN105687117A (en) 2016-06-22

Family

ID=56942144

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410689383.8A Pending CN105687117A (en) 2014-11-26 2014-11-26 Method for producing lauryl sorbitan polyoxyethylene ether iodine complex gel

Country Status (1)

Country Link
CN (1) CN105687117A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103007365A (en) * 2011-09-20 2013-04-03 天津博克尼科技发展有限公司 Iodine-containing medical lubrication gel
CN103006462A (en) * 2011-09-20 2013-04-03 天津博克尼科技发展有限公司 Iodine-containing sterilization type face cleaning liquid
CN103006464A (en) * 2011-09-20 2013-04-03 天津博克尼科技发展有限公司 Iodine-containing disinfection hand cleaner without water
CN103012767A (en) * 2011-09-20 2013-04-03 天津博克尼科技发展有限公司 Lauryl sorbitan ester polyoxyethylene ether iodine complex

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103007365A (en) * 2011-09-20 2013-04-03 天津博克尼科技发展有限公司 Iodine-containing medical lubrication gel
CN103006462A (en) * 2011-09-20 2013-04-03 天津博克尼科技发展有限公司 Iodine-containing sterilization type face cleaning liquid
CN103006464A (en) * 2011-09-20 2013-04-03 天津博克尼科技发展有限公司 Iodine-containing disinfection hand cleaner without water
CN103012767A (en) * 2011-09-20 2013-04-03 天津博克尼科技发展有限公司 Lauryl sorbitan ester polyoxyethylene ether iodine complex

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
胡英等: "《药物制剂》", 28 February 2013, 中国医药科技出版社 *

Similar Documents

Publication Publication Date Title
NZ610977A (en) Use of encapsulated oil in dough preparation
WO2015028892A3 (en) Reaction platform and method for making pollen based materials in combination with beeswax and uses thereof
KR20140114492A (en) Composition from natural material for hair loss or hair growth effect
CN105687117A (en) Method for producing lauryl sorbitan polyoxyethylene ether iodine complex gel
CN105687232A (en) Method for producing polyglycerin fatty acid ester iodine complex gel
CN105687120A (en) Method for producing laurylamine polyoxyethylene ether iodine complex gel
CN105687123A (en) Preparation method of polyoxyethylene stearate (40) ether-iodine complex gel
CN105687119A (en) Method for producing octadecanol polyoxyethylene (30) ether iodine complex gel
CN105687121A (en) Method for producing alkylphenol polyoxyethylene iodine complex gel
CN105640872A (en) Preparation method of lauryl alcohol amide polyoxyethylene ether iodine complex gel
CN105687116A (en) Method for producing cocamidopropyl betaine iodine complex gel
CN105687122A (en) Hydroxyethyl oleic imidazoline betaine iodine complex gel manufacturing method
CN105687115A (en) N-dodecyl sodium alanine iodine complex gel manufacturing method
CN105687233A (en) Method for producing coco trimethyl ammonium chloride iodine complex gel
CN105687118A (en) Method for producing glycerin polyether iodine complex gel
CN104560594A (en) A preparing method of an edible-vinegar capsule
CN108707502B (en) Preparation method and application of alligator oil
CN102988276B (en) A kind of Terbinafine hydrochloride emulsifiable paste prescription and preparation technology thereof
CN103393744A (en) Preparation method of externally used purple tincture for eliminating tinea
CN104371881A (en) Method for producing red bayberry wine
CN103908425B (en) A kind of antifungal flutrimazole ointment formulation and preparation technology thereof
CN1314398C (en) Cream for treating dexmatosis, and its prepn. method
CN105395471A (en) External use emulsifiable paste for treating skin diseases and with econazole nitrate as active component and preparation method
CN106924279B (en) Application of TTS-12 of caltrops, traditional Chinese medicine gel for inhibiting trichophyton mentagrophytes and preparation method of traditional Chinese medicine gel
CN104523711B (en) Ketone Kang Tasuo emulsifiable pastes and preparation method 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
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20160622