CN103254198A - Urotropine production method - Google Patents

Urotropine production method Download PDF

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Publication number
CN103254198A
CN103254198A CN 201210038685 CN201210038685A CN103254198A CN 103254198 A CN103254198 A CN 103254198A CN 201210038685 CN201210038685 CN 201210038685 CN 201210038685 A CN201210038685 A CN 201210038685A CN 103254198 A CN103254198 A CN 103254198A
Authority
CN
China
Prior art keywords
urotropine
production method
paraformaldehyde
byproduct
environmental protection
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
CN 201210038685
Other languages
Chinese (zh)
Inventor
陶坤山
张建华
张继钱
于海军
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.)
DONGCHANG CHEMICAL INDUSTRY Co Ltd NANTONG CITY
Original Assignee
DONGCHANG CHEMICAL INDUSTRY Co Ltd NANTONG CITY
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 DONGCHANG CHEMICAL INDUSTRY Co Ltd NANTONG CITY filed Critical DONGCHANG CHEMICAL INDUSTRY Co Ltd NANTONG CITY
Priority to CN 201210038685 priority Critical patent/CN103254198A/en
Publication of CN103254198A publication Critical patent/CN103254198A/en
Pending legal-status Critical Current

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Abstract

The invention discloses an urotropine production method. The method comprises the following steps: dissolving a glyphosate pesticide byproduct leftover containing formaldehyde, urotropine and paraformaldehyde in water, letting in ammonia gas, gradually heating to 60-80DEG C, controlling the pH value in a range of 9-10, cooling to below 20DEG C, maintaining the temperature constant for 1h, carrying out pumping filtration, and centrifuging to obtain urotropine having a crystal content of 96% or more. The method has the advantages of simplicity, easy operation, and good environmental protection property.

Description

The production method of urotropine
Technical field
The present invention relates to a kind of production method of urotropine.
Background technology
Existing urotropine production method complexity, not easy to operate, yield is low, and environmental pollution is big.
Summary of the invention
The object of the present invention is to provide that a kind of method is easy, easy to operate, the production method of the urotropine of environmental protection.
Technical solution of the present invention is:
A kind of production method of urotropine, it is characterized in that: the glyphosate agricultural chemicals byproduct pin material that will contain formaldehyde, urotropine, Paraformaldehyde 96, use water dissolution, feed ammonia, be warming up to 60 ~ 80 ℃ gradually, control pH9 ~ 10, be cooled to below 20 ℃, be incubated 1 hour, suction filtration, centrifugal gets the urotropine of brilliant content 〉=96%.
The inventive method is easy, easy to operate, the feature of environmental protection is good.
The invention will be further described below in conjunction with embodiment.
Embodiment
A kind of production method of urotropine, the agricultural chemicals byproduct pin material such as glyphosate that will contain formaldehyde, urotropine, Paraformaldehyde 96, use water dissolution, feed ammonia, be warming up to 60 ~ 80 ℃ gradually, control pH9 ~ 10, be cooled to below 20 ℃, be incubated 1 hour, suction filtration, centrifugal gets the urotropine of brilliant content 〉=96%.

Claims (1)

1. the production method of a urotropine, it is characterized in that: the glyphosate agricultural chemicals byproduct pin material that will contain formaldehyde, urotropine, Paraformaldehyde 96, use water dissolution, feed ammonia, be warming up to 60 ~ 80 ℃ gradually, control pH9 ~ 10, be cooled to below 20 ℃, be incubated 1 hour, suction filtration, centrifugal gets the urotropine of brilliant content 〉=96%.
CN 201210038685 2012-02-21 2012-02-21 Urotropine production method Pending CN103254198A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201210038685 CN103254198A (en) 2012-02-21 2012-02-21 Urotropine production method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201210038685 CN103254198A (en) 2012-02-21 2012-02-21 Urotropine production method

Publications (1)

Publication Number Publication Date
CN103254198A true CN103254198A (en) 2013-08-21

Family

ID=48958461

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201210038685 Pending CN103254198A (en) 2012-02-21 2012-02-21 Urotropine production method

Country Status (1)

Country Link
CN (1) CN103254198A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109476673A (en) * 2016-06-03 2019-03-15 雅宝公司 Method for generating hexamine mandelate

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109476673A (en) * 2016-06-03 2019-03-15 雅宝公司 Method for generating hexamine mandelate
CN109476673B (en) * 2016-06-03 2021-10-22 格雷斯公司 Method for producing urotropin mandelate

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C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20130821