JPS6445349A - Production of dl-lysine - Google Patents

Production of dl-lysine

Info

Publication number
JPS6445349A
JPS6445349A JP20212587A JP20212587A JPS6445349A JP S6445349 A JPS6445349 A JP S6445349A JP 20212587 A JP20212587 A JP 20212587A JP 20212587 A JP20212587 A JP 20212587A JP S6445349 A JPS6445349 A JP S6445349A
Authority
JP
Japan
Prior art keywords
acid
lysine
equivalent
1mol
optically active
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
JP20212587A
Other languages
Japanese (ja)
Inventor
Takae Ono
Shoji Morita
Toshihiro Fujino
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.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
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 Toray Industries Inc filed Critical Toray Industries Inc
Priority to JP20212587A priority Critical patent/JPS6445349A/en
Publication of JPS6445349A publication Critical patent/JPS6445349A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain DL-lysine useful as a basic salt-forming agent for an acidic drug such as aspirin, with economical means in high purity, by racemizing an optically active lysine and treating with a free acid. CONSTITUTION:1mol. (2 equivalent) of an optically active lysine is racemized at 130-200 deg.C by using 0.4-5 times weight of water in the presence of 1-2 equivalent of an acid (e.g. hydrochloric acid). To improve the quality of the product, the racemization reaction liquid is added with 2.1-3 equivalent [based on 1mol. (2 equivalent) of lysine] of an acid (e.g. hydrochloric acid) and treated with the acid at 120-180 deg.C. If necessary, the reaction product is subjected to activated carbon treatment for removing coloring impurities, ion exchange treatment to remove the acid and obtain free DL-lysine, etc.
JP20212587A 1987-08-13 1987-08-13 Production of dl-lysine Pending JPS6445349A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20212587A JPS6445349A (en) 1987-08-13 1987-08-13 Production of dl-lysine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20212587A JPS6445349A (en) 1987-08-13 1987-08-13 Production of dl-lysine

Publications (1)

Publication Number Publication Date
JPS6445349A true JPS6445349A (en) 1989-02-17

Family

ID=16452377

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20212587A Pending JPS6445349A (en) 1987-08-13 1987-08-13 Production of dl-lysine

Country Status (1)

Country Link
JP (1) JPS6445349A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106187799A (en) * 2016-06-30 2016-12-07 宜兴市前成生物有限公司 A kind of method preparing DL lysine hydrochloride

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106187799A (en) * 2016-06-30 2016-12-07 宜兴市前成生物有限公司 A kind of method preparing DL lysine hydrochloride

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