JPS5925324A - メナジオンとチアミンとを相互に安定化するアダクト - Google Patents

メナジオンとチアミンとを相互に安定化するアダクト

Info

Publication number: JPS5925324A
Authority: JP; Japan
Prior art keywords: thiamine; adduct; menadione; methidione; thiamine hydrochloride
Prior art date: 1982-06-24
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

JP58111975A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0567638B2 (2

Inventor

ジヨバンニ・ゲリ−

アレサンドロ・バルボン

ルチアノ・コンチ

ルイジ・オリアリ

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.)

Luigi Stoppani SpA

Original Assignee

Luigi Stoppani SpA

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.)

1982-06-24

Filing date

1983-06-23

Publication date

1984-02-09

1983-06-23 Application filed by Luigi Stoppani SpA filed Critical Luigi Stoppani SpA

1984-02-09 Publication of JPS5925324A publication Critical patent/JPS5925324A/ja

1993-09-27 Publication of JPH0567638B2 publication Critical patent/JPH0567638B2/ja

Status Granted legal-status Critical Current

Links

MJVAVZPDRWSRRC-UHFFFAOYSA-N Menadione Chemical compound C1=CC=C2C(=O)C(C)=CC(=O)C2=C1 MJVAVZPDRWSRRC-UHFFFAOYSA-N 0.000 title claims description 17
239000011721 thiamine Substances 0.000 title claims description 16
JZRWCGZRTZMZEH-UHFFFAOYSA-N Thiamine Natural products CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N JZRWCGZRTZMZEH-UHFFFAOYSA-N 0.000 title claims description 15
229960003495 thiamine Drugs 0.000 title claims description 14
235000019157 thiamine Nutrition 0.000 title claims description 13
KYMBYSLLVAOCFI-UHFFFAOYSA-N thiamine Chemical compound CC1=C(CCO)SCN1CC1=CN=C(C)N=C1N KYMBYSLLVAOCFI-UHFFFAOYSA-N 0.000 title claims description 11
235000012711 vitamin K3 Nutrition 0.000 title claims description 9
239000011652 vitamin K3 Substances 0.000 title claims description 9
229940041603 vitamin k 3 Drugs 0.000 title claims description 9
230000000087 stabilizing effect Effects 0.000 title description 4
DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 claims description 20
229960000344 thiamine hydrochloride Drugs 0.000 claims description 19
235000019190 thiamine hydrochloride Nutrition 0.000 claims description 19
239000011747 thiamine hydrochloride Substances 0.000 claims description 19
102220133487 rs149819112 Human genes 0.000 claims 1
238000001228 spectrum Methods 0.000 description 14
150000001875 compounds Chemical class 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
239000000047 product Substances 0.000 description 9
239000000203 mixture Substances 0.000 description 7
230000006641 stabilisation Effects 0.000 description 6
238000011105 stabilization Methods 0.000 description 6
230000000694 effects Effects 0.000 description 5
229940088594 vitamin Drugs 0.000 description 5
229930003231 vitamin Natural products 0.000 description 5
235000013343 vitamin Nutrition 0.000 description 5
239000011782 vitamin Substances 0.000 description 5
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
150000003722 vitamin derivatives Chemical class 0.000 description 4
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 3
239000006069 physical mixture Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 3
238000003756 stirring Methods 0.000 description 3
230000001225 therapeutic effect Effects 0.000 description 3
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
235000009754 Vitis X bourquina Nutrition 0.000 description 2
235000012333 Vitis X labruscana Nutrition 0.000 description 2
240000006365 Vitis vinifera Species 0.000 description 2
235000014787 Vitis vinifera Nutrition 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
230000032683 aging Effects 0.000 description 2
238000001035 drying Methods 0.000 description 2
235000019441 ethanol Nutrition 0.000 description 2
229960004051 menadione sodium bisulfite Drugs 0.000 description 2
XDPFHGWVCTXHDX-UHFFFAOYSA-M menadione sodium sulfonate Chemical compound [Na+].C1=CC=C2C(=O)C(C)(S([O-])(=O)=O)CC(=O)C2=C1 XDPFHGWVCTXHDX-UHFFFAOYSA-M 0.000 description 2
238000003825 pressing Methods 0.000 description 2
235000010265 sodium sulphite Nutrition 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
238000005406 washing Methods 0.000 description 2
BDEDPKFUFGCVCJ-UHFFFAOYSA-N 3,6-dihydroxy-8,8-dimethyl-1-oxo-3,4,7,9-tetrahydrocyclopenta[h]isochromene-5-carbaldehyde Chemical compound O=C1OC(O)CC(C(C=O)=C2O)=C1C1=C2CC(C)(C)C1 BDEDPKFUFGCVCJ-UHFFFAOYSA-N 0.000 description 1
-1 4-amino-2-methyl-5- Pyrimidinyl-methyl Chemical group 0.000 description 1
108010068370 Glutens Proteins 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
229930003270 Vitamin B Natural products 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
229960001231 choline Drugs 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000012530 fluid Substances 0.000 description 1
235000021312 gluten Nutrition 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
238000009776 industrial production Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000000034 method Methods 0.000 description 1
239000002245 particle Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
125000001990 thiamine group Chemical group 0.000 description 1
WEQHQGJDZLDFID-UHFFFAOYSA-J thorium(iv) chloride Chemical compound Cl[Th](Cl)(Cl)Cl WEQHQGJDZLDFID-UHFFFAOYSA-J 0.000 description 1
235000019156 vitamin B Nutrition 0.000 description 1
239000011720 vitamin B Substances 0.000 description 1
150000003716 vitamin K3 derivatives Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D415/00—Heterocyclic compounds containing the thiamine skeleton
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/174—Vitamins

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Food Science & Technology (AREA)
Engineering & Computer Science (AREA)
Zoology (AREA)
Animal Husbandry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Fodder In General (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

JP58111975A 1982-06-24 1983-06-23 メナジオンとチアミンとを相互に安定化するアダクト Granted JPS5925324A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
IT22051A/82		1982-06-24
IT22051/82A IT1159074B (it)	1982-06-24	1982-06-24	Composto di addizione fra menadione e tiamina a reciproca stabilizzazione

Publications (2)

Publication Number	Publication Date
JPS5925324A true JPS5925324A (ja)	1984-02-09
JPH0567638B2 JPH0567638B2 (2)	1993-09-27

Family

ID=11190742

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP58111975A Granted JPS5925324A (ja)	1982-06-24	1983-06-23	メナジオンとチアミンとを相互に安定化するアダクト

Country Status (11)

Country	Link
US (1)	US4568745A (2)
EP (1)	EP0098995B1 (2)
JP (1)	JPS5925324A (2)
AR (1)	AR230185A1 (2)
AT (1)	ATE25979T1 (2)
CA (1)	CA1216794A (2)
DE (1)	DE3370330D1 (2)
ES (1)	ES8507453A1 (2)
IE (1)	IE55626B1 (2)
IL (1)	IL69035A0 (2)
IT (1)	IT1159074B (2)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4808602A (en) *	1986-02-27	1989-02-28	Heterochemical Corporation	Derivatives based upon pyrido-menadione adducts and use thereof as feed premixes
BR112018014272B1 (pt)	2016-02-12	2021-12-28	Akzo Nobel Chemicals International B.V.	Processo de preparação de etilenoaminas
BR112018014270B1 (pt)	2016-02-12	2022-10-11	Akzo Nobel Chemicals International B.V.	Processo de preparação de etilenoaminas
MX390660B (es)	2016-02-12	2025-03-21	Akzo Nobel Chemicals Int Bv	Proceso para preparar etilenaminas superiores y derivados de etilenamina.
TWI768076B (zh)	2017-07-10	2022-06-21	荷蘭商安科智諾貝爾化學國際公司	製造直鏈及非直鏈伸乙基胺混合物之方法
TWI762670B (zh)	2017-07-10	2022-05-01	荷蘭商安科智諾貝爾化學國際公司	製備較高分子量伸乙基胺或其脲衍生物之方法
CN110959004B (zh)	2017-07-10	2023-09-12	诺力昂化学品国际有限公司	制备亚乙基胺和亚乙基胺衍生物的方法
TWI762669B (zh)	2017-07-10	2022-05-01	荷蘭商安科智諾貝爾化學國際公司	製造較高分子量伸乙基胺之方法
CN107501254A (zh) *	2017-08-15	2017-12-22	江西森泰药业有限公司	饲料添加剂维生素b1的制备工艺

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB685667A (en) *	1949-12-05	1953-01-07	Bayer Ag	A sparingly soluble new vitamin b salt and foodstuffs enriched therewith
US3931152A (en) *	1974-01-29	1976-01-06	American Cyanamid Company	2-(1,3-Diazacycloalkenyl)-2-hydrazones of substituted chalcones
US4006234A (en) *	1974-12-18	1977-02-01	American Cyanamid Company	Substituted 2-benzofuranyl propenones as anti-tubercular agents
JPS5231981A (en) *	1975-08-18	1977-03-10	Takeda Chem Ind Ltd	Microcapsule preparation method
GB2047739A (en) *	1979-04-27	1980-12-03	Roche Products Ltd	Nutrient medium

1982
- 1982-06-24 IT IT22051/82A patent/IT1159074B/it active
1983
- 1983-06-18 EP EP83105975A patent/EP0098995B1/en not_active Expired
- 1983-06-18 AT AT83105975T patent/ATE25979T1/de not_active IP Right Cessation
- 1983-06-18 DE DE8383105975T patent/DE3370330D1/de not_active Expired
- 1983-06-21 IL IL69035A patent/IL69035A0/xx unknown
- 1983-06-22 US US06/506,847 patent/US4568745A/en not_active Expired - Fee Related
- 1983-06-23 ES ES523528A patent/ES8507453A1/es not_active Expired
- 1983-06-23 JP JP58111975A patent/JPS5925324A/ja active Granted
- 1983-06-24 IE IE1482/83A patent/IE55626B1/en not_active IP Right Cessation
- 1983-06-24 CA CA000431183A patent/CA1216794A/en not_active Expired
- 1983-06-24 AR AR293432A patent/AR230185A1/es active

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS *

Also Published As

Publication number	Publication date
EP0098995B1 (en)	1987-03-18
US4568745A (en)	1986-02-04
IE831482L (en)	1983-12-24
IL69035A0 (en)	1983-10-31
IE55626B1 (en)	1990-12-05
IT1159074B (it)	1987-02-25
DE3370330D1 (en)	1987-04-23
AR230185A1 (es)	1984-03-01
CA1216794A (en)	1987-01-20
ATE25979T1 (de)	1987-04-15
EP0098995A1 (en)	1984-01-25
ES523528A0 (es)	1985-10-01
JPH0567638B2 (2)	1993-09-27
ES8507453A1 (es)	1985-10-01
IT8222051A0 (it)	1982-06-24

Publication	Publication Date	Title
DE69115790T2 (de)	1996-05-23	Allosterischer hämoglobin-modifikator
Barnes et al.	1973	Estimation of lipids in marine animals and tissues: detailed investigation of the sulphophosphovanilun method for ‘total’lipids
DE1644306B2 (de)	1976-05-06	Basische anthrachinon- und nitrofarbstoffe und verfahren zu deren herstellung
JPS5925324A (ja)	1984-02-09	メナジオンとチアミンとを相互に安定化するアダクト
DE848011C (de)	1952-09-18	Verfahren zur Herstellung von photographischen Farbbildern
DE1801278A1 (de)	1969-06-26	Bilirubin-Diagnostikum
Caldwell et al.	1952	Crystalline Pancreatic Amylase. II. Improved Method for its Preparation from Hog Pancreas Glands and Additional Studies of its Properties1
KR880001282A (ko)	1988-04-22	옥사자포스포린 용액 및 이의 제조방법
Hess et al.	1952	The isolation of chondroitin sulfuric acid from dentin
DE1569790A1 (de)	1970-04-09	Verfahren zur Herstellung von quaternaeren Cycloammoniumsalzen und ihren Kondensationsprodukten
Chibnall et al.	1939	The glutamic acid of tumour proteins
DE2422069A1 (de)	1974-12-05	Tetrazolium-c-oxybetainverbindungen und ihre verwendung als schleierverhuetungsmittel
ARNETT et al.	1962	Quantitative Estimates of the Strong Electron Donor Properties of Metallocenyl Nuclei1, 2
Cox et al.	1968	The molecular weights of porcine plasma high density lipoprotein and its subunits
Booth et al.	1954	A spectroscopic study of the nature of the complexes of purines with aromatic compounds
DE69118520T2 (de)	1996-08-29	Sechsbindige liganden für radiographische abbildungsagenzien
DE2407899C3 (de)	1978-09-28	Fluoreszenzmarkierung eines eine primäre Aminogruppe enthaltenden Materials
Collins	1954	The chemistry of vision
Hill et al.	1922	Researches on Thiocyanates and Isothiocyanates. Xv. The Nature of the Intramolecular Rearrangement of Isothiocyanato-Acetanilides
Li	1944	Electrophoresis of Rat Sera1
Baldwin et al.	1958	Carcinogenicity of tricycloquinazoline
Stasney et al.	1942	Serial bone marrow studies in pernicious anemia. III. Occurrence of protoporphyrin in human bone marrow
DE726082C (de)	1942-10-06	Verfahren zum orthochromatischen Sensibilisieren von Silberhalogen-Emulsionen
DE1644404A1 (de)	1970-12-17	Neuartige Anthrachinonfarben und Zwischenprodukte
DE1017616B (de)	1957-10-17	Verfahren zur Herstellung von 1, 3, 5-Tri-(4-sulfamyl-phenylamino)-triazin