CN105296207A - Experimental utensil cleaning liquid for cytobiological and preparation method of experimental utensil cleaning liquid - Google Patents
Experimental utensil cleaning liquid for cytobiological and preparation method of experimental utensil cleaning liquid Download PDFInfo
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- CN105296207A CN105296207A CN201510880815.8A CN201510880815A CN105296207A CN 105296207 A CN105296207 A CN 105296207A CN 201510880815 A CN201510880815 A CN 201510880815A CN 105296207 A CN105296207 A CN 105296207A
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Abstract
The invention discloses experimental utensil cleaning liquid for cytobiological and a preparation method of the experimental utensil cleaning liquid. The experimental utensil cleaning liquid comprises the following components in parts by mass: 52-56 parts of sodium dichromate, 54-58 parts of titanium isopropylate, 50-54 parts of methylene glycol ethyl ether, 54-58 parts of alkanol phosphate, 50-54 parts of hydroxyethyl ethylenediamine, 54-58 parts of glycerindiacetate, 50-54 parts of potassium alkyl phosphate ester, 56-60 parts of benzoic acid, 50-54 parts of dichlorotetrafluoroethane, 54-58 parts of nonylphenol polyoxyethylene ether, 50-54 parts of polyoxyethylene stearate, 54-58 parts of lauramidopropyl betaine, 50-54 parts of sodium hexametaphosphate, 54-58 parts of mercaptobenzothiazole, 50-54 parts of tri-sodium nitrilotriacetate, 54-58 parts of triethanolamine, 50-54 parts of chlorothalonil, 54-58 parts of permethrin, 50-54 parts of dodecyl dimethyl benzyl ammonium bromide, 54-58 parts of olein, 50-54 parts of diacetylglycine and 10000-20000 parts of deionized water.
Description
Technical field
The present invention relates to a kind of cytobiology experimental apparatus scavenging solution and preparation method thereof, belong to technical field of cell biology.
Background technology
In cytobiology, often need to carry out various experiment, need to use various experimental apparatus in these experiments, generally after testing, need to carry out clean for these experimental apparatus, to obtain better clean effect, convenient realize experimental apparatus cleaning better, facilitate and follow-uply carry out experiment, general clean mode, cleaning performance is not good, and being necessary provides a kind of suitable clean liquid.
Summary of the invention
The object of the present invention is to provide a kind of cytobiology experimental apparatus scavenging solution and preparation method thereof, to realize Cell Biology Experiment utensil clean better.
The technical solution adopted for the present invention to solve the technical problems is: a kind of cytobiology experimental apparatus scavenging solution, is made up of the component of following mass fraction: sodium dichromate 99 52 ~ 56 parts, titanium isopropylate 54 ~ 58 parts, methylene glycol ethyl ether 50 ~ 54 parts, alkanol phosphoric acid ester 54 ~ 58 parts, hydroxyethylethylene diamine 50 ~ 54 parts, glyceryl diacetate 54 ~ 58 parts, potassium alkyl phosphate 50 ~ 54 parts, M-nitro benzoic acid 56 ~ 60 parts, dichloro tetrafluoro ethane 50 ~ 54 parts, polyoxyethylene nonylphenol ether 54 ~ 58 parts, polyethylene glycol stearate 50 ~ 54 parts, lauryl amidopropyl betaine 54 ~ 58 parts, Sodium hexametaphosphate 99 50 ~ 54 parts, mercapto benzothiazole 54 ~ 58 parts, nitrilotriacetic acid(NTA) trisodium 50 ~ 54 parts, trolamine 54 ~ 58 parts, m-tetrachlorophthalodinitrile 50 ~ 54 parts, permethrin 54 ~ 58 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 50 ~ 54 parts, olein 54 ~ 58 parts, glyceryl diacetate 50 ~ 54 parts, tosic acid 54 ~ 58 parts, silver ion antimicrobial agent 50 ~ 54 parts, deionized water 10000 ~ 20000 parts.
Further, above-mentioned cytobiology experimental apparatus scavenging solution, be made up of the component of following mass fraction: sodium dichromate 99 52 parts, titanium isopropylate 54 parts, methylene glycol ethyl ether 50 parts, alkanol phosphoric acid ester 54 parts, hydroxyethylethylene diamine 50 parts, glyceryl diacetate 54 parts, potassium alkyl phosphate 50 parts, M-nitro benzoic acid 56 parts, dichloro tetrafluoro ethane 50 parts, polyoxyethylene nonylphenol ether 54 parts, polyethylene glycol stearate 50 parts, lauryl amidopropyl betaine 54 parts, Sodium hexametaphosphate 99 50 parts, mercapto benzothiazole 54 parts, nitrilotriacetic acid(NTA) trisodium 50 parts, trolamine 54 parts, m-tetrachlorophthalodinitrile 50 parts, permethrin 54 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 50 parts, olein 54 parts, glyceryl diacetate 50 parts, tosic acid 54 parts, silver ion antimicrobial agent 50 parts, deionized water 10000 parts.
Further, above-mentioned cytobiology experimental apparatus scavenging solution, be made up of the component of following mass fraction: sodium dichromate 99 54 parts, titanium isopropylate 56 parts, methylene glycol ethyl ether 52 parts, alkanol phosphoric acid ester 56 parts, hydroxyethylethylene diamine 52 parts, glyceryl diacetate 56 parts, potassium alkyl phosphate 52 parts, M-nitro benzoic acid 58 parts, dichloro tetrafluoro ethane 52 parts, polyoxyethylene nonylphenol ether 56 parts, polyethylene glycol stearate 52 parts, lauryl amidopropyl betaine 56 parts, Sodium hexametaphosphate 99 52 parts, mercapto benzothiazole 56 parts, nitrilotriacetic acid(NTA) trisodium 52 parts, trolamine 56 parts, m-tetrachlorophthalodinitrile 52 parts, permethrin 56 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 52 parts, olein 56 parts, glyceryl diacetate 52 parts, tosic acid 56 parts, silver ion antimicrobial agent 52 parts, deionized water 15000 parts.
Further, above-mentioned cytobiology experimental apparatus scavenging solution, be made up of the component of following mass fraction: sodium dichromate 99 56 parts, titanium isopropylate 58 parts, methylene glycol ethyl ether 54 parts, alkanol phosphoric acid ester 58 parts, hydroxyethylethylene diamine 54 parts, glyceryl diacetate 58 parts, potassium alkyl phosphate 54 parts, M-nitro benzoic acid 60 parts, dichloro tetrafluoro ethane 54 parts, polyoxyethylene nonylphenol ether 58 parts, polyethylene glycol stearate 54 parts, lauryl amidopropyl betaine 58 parts, Sodium hexametaphosphate 99 54 parts, mercapto benzothiazole 58 parts, nitrilotriacetic acid(NTA) trisodium 54 parts, trolamine 58 parts, m-tetrachlorophthalodinitrile 54 parts, permethrin 58 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 54 parts, olein 58 parts, glyceryl diacetate 54 parts, tosic acid 58 parts, silver ion antimicrobial agent 54 parts, deionized water 20000 parts.
Further, above-mentioned cytobiology experimental apparatus scavenging solution preparation method step is as follows:
(1) by the sodium dichromate 99 of described mass fraction, titanium isopropylate, methylene glycol ethyl ether, alkanol phosphoric acid ester, hydroxyethylethylene diamine, glyceryl diacetate, potassium alkyl phosphate, M-nitro benzoic acid, dichloro tetrafluoro ethane, polyoxyethylene nonylphenol ether, polyethylene glycol stearate, lauryl amidopropyl betaine, Sodium hexametaphosphate 99, mercapto benzothiazole, nitrilotriacetic acid(NTA) trisodium, trolamine, m-tetrachlorophthalodinitrile, permethrin, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium, tosic acid, silver ion antimicrobial agent adds in the deionized water of above-mentioned mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20 ~ 40KHz, rate of dispersion about 5000 ~ 5400r/min, jitter time is 30 ~ 60min,
(2) add the olein of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20 ~ 35KHz, rate of dispersion about 4800 ~ 5200r/min, and jitter time is 30 ~ 50min;
(3) add the glyceryl diacetate of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20 ~ 30KHz, rate of dispersion about 4600 ~ 4800r/min, and jitter time is 20 ~ 40min; Mix rear obtained this product.
The invention has the beneficial effects as follows: this cytobiology experimental apparatus scavenging solution process of preparing is simple, clean-out system of the present invention has good cleansing power, there is antibacterial and mouldproof and become effect, be applicable to cleaning cytobiology experimental apparatus, improve cleaning performance.
Embodiment
Below in conjunction with embodiment, the present invention is further described.
embodiment 1
Cytobiology in the present embodiment experimental apparatus scavenging solution, be made up of the component of following mass fraction: sodium dichromate 99 52 parts, titanium isopropylate 54 parts, methylene glycol ethyl ether 50 parts, alkanol phosphoric acid ester 54 parts, hydroxyethylethylene diamine 50 parts, glyceryl diacetate 54 parts, potassium alkyl phosphate 50 parts, M-nitro benzoic acid 56 parts, dichloro tetrafluoro ethane 50 parts, polyoxyethylene nonylphenol ether 54 parts, polyethylene glycol stearate 50 parts, lauryl amidopropyl betaine 54 parts, Sodium hexametaphosphate 99 50 parts, mercapto benzothiazole 54 parts, nitrilotriacetic acid(NTA) trisodium 50 parts, trolamine 54 parts, m-tetrachlorophthalodinitrile 50 parts, permethrin 54 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 50 parts, olein 54 parts, glyceryl diacetate 50 parts, tosic acid 54 parts, silver ion antimicrobial agent 50 parts, deionized water 10000 parts.
Above-mentioned cytobiology experimental apparatus scavenging solution preparation method step is as follows:
(1) by the sodium dichromate 99 of described mass fraction, titanium isopropylate, methylene glycol ethyl ether, alkanol phosphoric acid ester, hydroxyethylethylene diamine, glyceryl diacetate, potassium alkyl phosphate, M-nitro benzoic acid, dichloro tetrafluoro ethane, polyoxyethylene nonylphenol ether, polyethylene glycol stearate, lauryl amidopropyl betaine, Sodium hexametaphosphate 99, mercapto benzothiazole, nitrilotriacetic acid(NTA) trisodium, trolamine, m-tetrachlorophthalodinitrile, permethrin, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium, tosic acid, silver ion antimicrobial agent adds in the deionized water of above-mentioned mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20kHz, rate of dispersion about 5400r/min, jitter time is 60min,
(2) add the olein of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20kHz, rate of dispersion about 5200r/min, and jitter time is 50min;
(3) add the glyceryl diacetate of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20kHz, rate of dispersion about 4800r/min, and jitter time is 40min; Mix rear obtained this product.
embodiment 2
Cytobiology in the present embodiment experimental apparatus scavenging solution, be made up of the component of following mass fraction: sodium dichromate 99 54 parts, titanium isopropylate 56 parts, methylene glycol ethyl ether 52 parts, alkanol phosphoric acid ester 56 parts, hydroxyethylethylene diamine 52 parts, glyceryl diacetate 56 parts, potassium alkyl phosphate 52 parts, M-nitro benzoic acid 58 parts, dichloro tetrafluoro ethane 52 parts, polyoxyethylene nonylphenol ether 56 parts, polyethylene glycol stearate 52 parts, lauryl amidopropyl betaine 56 parts, Sodium hexametaphosphate 99 52 parts, mercapto benzothiazole 56 parts, nitrilotriacetic acid(NTA) trisodium 52 parts, trolamine 56 parts, m-tetrachlorophthalodinitrile 52 parts, permethrin 56 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 52 parts, olein 56 parts, glyceryl diacetate 52 parts, tosic acid 56 parts, silver ion antimicrobial agent 52 parts, deionized water 15000 parts.
Above-mentioned cytobiology experimental apparatus scavenging solution preparation method step is as follows:
(1) by the sodium dichromate 99 of described mass fraction, titanium isopropylate, methylene glycol ethyl ether, alkanol phosphoric acid ester, hydroxyethylethylene diamine, glyceryl diacetate, potassium alkyl phosphate, M-nitro benzoic acid, dichloro tetrafluoro ethane, polyoxyethylene nonylphenol ether, polyethylene glycol stearate, lauryl amidopropyl betaine, Sodium hexametaphosphate 99, mercapto benzothiazole, nitrilotriacetic acid(NTA) trisodium, trolamine, m-tetrachlorophthalodinitrile, permethrin, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium, tosic acid, silver ion antimicrobial agent adds in the deionized water of above-mentioned mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 30kHz, rate of dispersion about 5200r/min, jitter time is 45min,
(2) add the olein of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 27kHz, rate of dispersion about 5000r/min, and jitter time is 40min;
(3) add the glyceryl diacetate of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 25kHz, rate of dispersion about 4700r/min, and jitter time is 30min; Mix rear obtained this product.
embodiment 3
Cytobiology in the present embodiment experimental apparatus scavenging solution, be made up of the component of following mass fraction: sodium dichromate 99 56 parts, titanium isopropylate 58 parts, methylene glycol ethyl ether 54 parts, alkanol phosphoric acid ester 58 parts, hydroxyethylethylene diamine 54 parts, glyceryl diacetate 58 parts, potassium alkyl phosphate 54 parts, M-nitro benzoic acid 60 parts, dichloro tetrafluoro ethane 54 parts, polyoxyethylene nonylphenol ether 58 parts, polyethylene glycol stearate 54 parts, lauryl amidopropyl betaine 58 parts, Sodium hexametaphosphate 99 54 parts, mercapto benzothiazole 58 parts, nitrilotriacetic acid(NTA) trisodium 54 parts, trolamine 58 parts, m-tetrachlorophthalodinitrile 54 parts, permethrin 58 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 54 parts, olein 58 parts, glyceryl diacetate 54 parts, tosic acid 58 parts, silver ion antimicrobial agent 54 parts, deionized water 20000 parts.
Above-mentioned cytobiology experimental apparatus scavenging solution preparation method step is as follows:
(1) by the sodium dichromate 99 of described mass fraction, titanium isopropylate, methylene glycol ethyl ether, alkanol phosphoric acid ester, hydroxyethylethylene diamine, glyceryl diacetate, potassium alkyl phosphate, M-nitro benzoic acid, dichloro tetrafluoro ethane, polyoxyethylene nonylphenol ether, polyethylene glycol stearate, lauryl amidopropyl betaine, Sodium hexametaphosphate 99, mercapto benzothiazole, nitrilotriacetic acid(NTA) trisodium, trolamine, m-tetrachlorophthalodinitrile, permethrin, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium, tosic acid, silver ion antimicrobial agent adds in the deionized water of above-mentioned mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 40kHz, rate of dispersion 5000r/min, jitter time is 30min,
(2) add the olein of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 35kHz, rate of dispersion 4800r/min, and jitter time is 30min;
(3) add the glyceryl diacetate of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 30kHz, rate of dispersion about 4600r/min, and jitter time is 20min; Mix rear obtained this product.
Performance measurement is carried out for the product in embodiment 1, embodiment 2 and embodiment 3 and certain commercially available prod.Measured data are as shown in table 1.
Table 1 the performance test results
Visible, clean-out system of the present invention has good cleansing power, has antibacterial and mouldproof and becomes effect.
Claims (5)
1. a cytobiology experimental apparatus scavenging solution, is characterized in that: be made up of the component of following mass fraction: sodium dichromate 99 52 ~ 56 parts, titanium isopropylate 54 ~ 58 parts, methylene glycol ethyl ether 50 ~ 54 parts, alkanol phosphoric acid ester 54 ~ 58 parts, hydroxyethylethylene diamine 50 ~ 54 parts, glyceryl diacetate 54 ~ 58 parts, potassium alkyl phosphate 50 ~ 54 parts, M-nitro benzoic acid 56 ~ 60 parts, dichloro tetrafluoro ethane 50 ~ 54 parts, polyoxyethylene nonylphenol ether 54 ~ 58 parts, polyethylene glycol stearate 50 ~ 54 parts, lauryl amidopropyl betaine 54 ~ 58 parts, Sodium hexametaphosphate 99 50 ~ 54 parts, mercapto benzothiazole 54 ~ 58 parts, nitrilotriacetic acid(NTA) trisodium 50 ~ 54 parts, trolamine 54 ~ 58 parts, m-tetrachlorophthalodinitrile 50 ~ 54 parts, permethrin 54 ~ 58 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 50 ~ 54 parts, olein 54 ~ 58 parts, glyceryl diacetate 50 ~ 54 parts, tosic acid 54 ~ 58 parts, silver ion antimicrobial agent 50 ~ 54 parts, deionized water 10000 ~ 20000 parts.
2. cytobiology experimental apparatus scavenging solution according to claim 1, it is characterized in that: described cytobiology experimental apparatus scavenging solution is made up of the component of following mass fraction: sodium dichromate 99 52 parts, titanium isopropylate 54 parts, methylene glycol ethyl ether 50 parts, alkanol phosphoric acid ester 54 parts, hydroxyethylethylene diamine 50 parts, glyceryl diacetate 54 parts, potassium alkyl phosphate 50 parts, M-nitro benzoic acid 56 parts, dichloro tetrafluoro ethane 50 parts, polyoxyethylene nonylphenol ether 54 parts, polyethylene glycol stearate 50 parts, lauryl amidopropyl betaine 54 parts, Sodium hexametaphosphate 99 50 parts, mercapto benzothiazole 54 parts, nitrilotriacetic acid(NTA) trisodium 50 parts, trolamine 54 parts, m-tetrachlorophthalodinitrile 50 parts, permethrin 54 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 50 parts, olein 54 parts, glyceryl diacetate 50 parts, tosic acid 54 parts, silver ion antimicrobial agent 50 parts, deionized water 10000 parts.
3. cytobiology experimental apparatus scavenging solution according to claim 1, it is characterized in that: described cytobiology experimental apparatus scavenging solution is made up of the component of following mass fraction: sodium dichromate 99 54 parts, titanium isopropylate 56 parts, methylene glycol ethyl ether 52 parts, alkanol phosphoric acid ester 56 parts, hydroxyethylethylene diamine 52 parts, glyceryl diacetate 56 parts, potassium alkyl phosphate 52 parts, M-nitro benzoic acid 58 parts, dichloro tetrafluoro ethane 52 parts, polyoxyethylene nonylphenol ether 56 parts, polyethylene glycol stearate 52 parts, lauryl amidopropyl betaine 56 parts, Sodium hexametaphosphate 99 52 parts, mercapto benzothiazole 56 parts, nitrilotriacetic acid(NTA) trisodium 52 parts, trolamine 56 parts, m-tetrachlorophthalodinitrile 52 parts, permethrin 56 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 52 parts, olein 56 parts, glyceryl diacetate 52 parts, tosic acid 56 parts, silver ion antimicrobial agent 52 parts, deionized water 15000 parts.
4. cytobiology experimental apparatus scavenging solution according to claim 1, it is characterized in that: described cytobiology experimental apparatus scavenging solution is made up of the component of following mass fraction: sodium dichromate 99 56 parts, titanium isopropylate 58 parts, methylene glycol ethyl ether 54 parts, alkanol phosphoric acid ester 58 parts, hydroxyethylethylene diamine 54 parts, glyceryl diacetate 58 parts, potassium alkyl phosphate 54 parts, M-nitro benzoic acid 60 parts, dichloro tetrafluoro ethane 54 parts, polyoxyethylene nonylphenol ether 58 parts, polyethylene glycol stearate 54 parts, lauryl amidopropyl betaine 58 parts, Sodium hexametaphosphate 99 54 parts, mercapto benzothiazole 58 parts, nitrilotriacetic acid(NTA) trisodium 54 parts, trolamine 58 parts, m-tetrachlorophthalodinitrile 54 parts, permethrin 58 parts, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium 54 parts, olein 58 parts, glyceryl diacetate 54 parts, tosic acid 58 parts, silver ion antimicrobial agent 54 parts, deionized water 20000 parts.
5. the experimental apparatus scavenging solution of the cytobiology according to Claims 1-4, is characterized in that: described cytobiology experimental apparatus scavenging solution preparation method step is as follows:
(1) by the sodium dichromate 99 of described mass fraction, titanium isopropylate, methylene glycol ethyl ether, alkanol phosphoric acid ester, hydroxyethylethylene diamine, glyceryl diacetate, potassium alkyl phosphate, M-nitro benzoic acid, dichloro tetrafluoro ethane, polyoxyethylene nonylphenol ether, polyethylene glycol stearate, lauryl amidopropyl betaine, Sodium hexametaphosphate 99, mercapto benzothiazole, nitrilotriacetic acid(NTA) trisodium, trolamine, m-tetrachlorophthalodinitrile, permethrin, bromination dodecyl dimethyl hexadecyldimethyl benzyl ammonium, tosic acid, silver ion antimicrobial agent adds in the deionized water of above-mentioned mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20 ~ 40KHz, rate of dispersion about 5000 ~ 5400r/min, jitter time is 30 ~ 60min,
(2) add the olein of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20 ~ 35KHz, rate of dispersion about 4800 ~ 5200r/min, and jitter time is 30 ~ 50min;
(3) add the glyceryl diacetate of described mass fraction, ultrasonic high speed dispersion, ultrasonic frequency is 20 ~ 30KHz, rate of dispersion about 4600 ~ 4800r/min, and jitter time is 20 ~ 40min; Mix rear obtained this product.
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| Application Number | Priority Date | Filing Date | Title |
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| CN201510880815.8A CN105296207A (en) | 2015-12-05 | 2015-12-05 | Experimental utensil cleaning liquid for cytobiological and preparation method of experimental utensil cleaning liquid |
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Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN1104423A (en) * | 1993-08-19 | 1995-07-05 | 花王株式会社 | Germicidal-disinfectant detergent composition |
| CN1270531A (en) * | 1997-07-21 | 2000-10-18 | 普罗格特-甘布尔公司 | Method for sanitization of substrates with deteragent compositions |
| CN1422165A (en) * | 2000-04-07 | 2003-06-04 | 新药研究(澳大利亚)有限公司 | Process and composition for cleaning medical instruments |
| CN103261392A (en) * | 2010-12-28 | 2013-08-21 | 花王株式会社 | Method for cleaning medical appliance |
| CN104031778A (en) * | 2014-06-12 | 2014-09-10 | 仇彩霞 | Culture dish cleaning solution and cleaning method |
| CN104073366A (en) * | 2013-12-05 | 2014-10-01 | 成都老肯科技股份有限公司 | Alkaline cleaner suitable for cleaning medical appliance and preparation method thereof |
-
2015
- 2015-12-05 CN CN201510880815.8A patent/CN105296207A/en active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1104423A (en) * | 1993-08-19 | 1995-07-05 | 花王株式会社 | Germicidal-disinfectant detergent composition |
| CN1270531A (en) * | 1997-07-21 | 2000-10-18 | 普罗格特-甘布尔公司 | Method for sanitization of substrates with deteragent compositions |
| CN1422165A (en) * | 2000-04-07 | 2003-06-04 | 新药研究(澳大利亚)有限公司 | Process and composition for cleaning medical instruments |
| CN103261392A (en) * | 2010-12-28 | 2013-08-21 | 花王株式会社 | Method for cleaning medical appliance |
| CN104073366A (en) * | 2013-12-05 | 2014-10-01 | 成都老肯科技股份有限公司 | Alkaline cleaner suitable for cleaning medical appliance and preparation method thereof |
| CN104031778A (en) * | 2014-06-12 | 2014-09-10 | 仇彩霞 | Culture dish cleaning solution and cleaning method |
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