NO121044B - - Google Patents

Download PDF

Info

Publication number: NO121044B
Authority: NO; Norway
Prior art keywords: aminoalkyl; titanate; solution; stable; stabilized
Prior art date: 1965-12-23

Application number

NO16610266A

Other languages

English (en)

Norwegian (no)

Inventor

L Bernardi

G Suchowsky

S Coda

L Pegrassi

Original Assignee

Farmaceutici Italia

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.)

1965-12-23

Filing date

1966-12-22

Publication date

1971-01-11

1966-12-22 Application filed by Farmaceutici Italia filed Critical Farmaceutici Italia

1971-01-11 Publication of NO121044B publication Critical patent/NO121044B/no

Links

-1 aminoalkyl titanate Chemical compound 0.000 claims description 17
RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 claims description 16
239000003381 stabilizer Substances 0.000 claims description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
125000004103 aminoalkyl group Chemical group 0.000 claims description 15
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims description 13
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 13
239000000600 sorbitol Substances 0.000 claims description 13
RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 claims description 8
239000000174 gluconic acid Substances 0.000 claims description 8
235000012208 gluconic acid Nutrition 0.000 claims description 8
150000005846 sugar alcohols Polymers 0.000 claims description 7
SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 claims description 6
CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 claims description 6
229960000367 inositol Drugs 0.000 claims description 6
CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 claims description 6
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims description 4
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 4
229930195725 Mannitol Natural products 0.000 claims description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 4
125000001931 aliphatic group Chemical group 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
239000008103 glucose Substances 0.000 claims description 4
239000000594 mannitol Substances 0.000 claims description 4
235000010355 mannitol Nutrition 0.000 claims description 4
WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 claims description 3
125000003172 aldehyde group Chemical group 0.000 claims description 3
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 2
229930006000 Sucrose Natural products 0.000 claims description 2
125000002723 alicyclic group Chemical group 0.000 claims description 2
125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
229920006395 saturated elastomer Polymers 0.000 claims description 2
239000005720 sucrose Substances 0.000 claims description 2
239000000243 solution Substances 0.000 description 32
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 18
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 15
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 15
239000007864 aqueous solution Substances 0.000 description 11
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 10
238000000034 method Methods 0.000 description 9
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 7
239000000203 mixture Substances 0.000 description 7
229910052719 titanium Inorganic materials 0.000 description 7
239000010936 titanium Substances 0.000 description 7
229960004418 trolamine Drugs 0.000 description 7
IHEDBVUTTQXGSJ-UHFFFAOYSA-M 2-[bis(2-oxidoethyl)amino]ethanolate;titanium(4+);hydroxide Chemical compound [OH-].[Ti+4].[O-]CCN(CC[O-])CC[O-] IHEDBVUTTQXGSJ-UHFFFAOYSA-M 0.000 description 6
VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 6
150000001875 compounds Chemical class 0.000 description 4
230000007062 hydrolysis Effects 0.000 description 4
238000006460 hydrolysis reaction Methods 0.000 description 4
150000003755 zirconium compounds Chemical class 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
239000012736 aqueous medium Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
150000002772 monosaccharides Chemical class 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
RGHNJXZEOKUKBD-MGCNEYSASA-N D-galactonic acid Chemical compound OC[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-MGCNEYSASA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000001414 amino alcohols Chemical class 0.000 description 2
LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 2
229940043276 diisopropanolamine Drugs 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
238000011105 stabilization Methods 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004753 textile Substances 0.000 description 2
229910052845 zircon Inorganic materials 0.000 description 2
YAXKTBLXMTYWDQ-UHFFFAOYSA-N 1,2,3-butanetriol Chemical compound CC(O)C(O)CO YAXKTBLXMTYWDQ-UHFFFAOYSA-N 0.000 description 1
239000004484 Briquette Substances 0.000 description 1
HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 description 1
229930194542 Keto Natural products 0.000 description 1
MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000013522 chelant Substances 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
125000004989 dicarbonyl group Chemical group 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000835 fiber Substances 0.000 description 1
FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
HOVAGTYPODGVJG-ZFYZTMLRSA-N methyl alpha-D-glucopyranoside Chemical compound CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HOVAGTYPODGVJG-ZFYZTMLRSA-N 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000011368 organic material Substances 0.000 description 1
IYVLHQRADFNKAU-UHFFFAOYSA-N oxygen(2-);titanium(4+);hydrate Chemical class O.[O-2].[O-2].[Ti+4] IYVLHQRADFNKAU-UHFFFAOYSA-N 0.000 description 1
HEBKCHPVOIAQTA-ZXFHETKHSA-N ribitol Chemical compound OC[C@H](O)[C@H](O)[C@H](O)CO HEBKCHPVOIAQTA-ZXFHETKHSA-N 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
150000003609 titanium compounds Chemical class 0.000 description 1
GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/12—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems
- C07D265/14—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D265/20—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in position 4
- C07D265/22—Oxygen atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/06—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings
- C07D265/08—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Epidemiology (AREA)
Life Sciences & Earth Sciences (AREA)
Pharmacology & Pharmacy (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Medicinal Chemistry (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO16610266A 1965-12-23 1966-12-22 NO121044B (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
IT1263865		1965-12-23
IT2238566		1966-09-14

Publications (1)

Publication Number	Publication Date
NO121044B true NO121044B (de)	1971-01-11

Family

ID=26326577

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO16610266A NO121044B (de)	1965-12-23	1966-12-22

Country Status (7)

Country	Link
AT (1)	AT264535B (de)
BE (1)	BE691641A (de)
ES (1)	ES334818A1 (de)
FI (1)	FI46729C (de)
IL (1)	IL27092A (de)
NO (1)	NO121044B (de)
SE (1)	SE316773B (de)

1966
- 1966-12-19 IL IL2709266A patent/IL27092A/xx unknown
- 1966-12-20 FI FI338866A patent/FI46729C/fi active
- 1966-12-21 AT AT1175266A patent/AT264535B/de active
- 1966-12-22 NO NO16610266A patent/NO121044B/no unknown
- 1966-12-22 SE SE1755966A patent/SE316773B/xx unknown
- 1966-12-22 BE BE691641D patent/BE691641A/xx unknown
- 1966-12-22 ES ES334818A patent/ES334818A1/es not_active Expired

Also Published As

Publication number	Publication date
DE1620436A1 (de)	1970-05-21
IL27092A (en)	1970-11-30
SE316773B (de)	1969-11-03
FI46729C (fi)	1973-06-11
FI46729B (de)	1973-02-28
AT264535B (de)	1968-09-10
BE691641A (de)	1967-06-22
ES334818A1 (es)	1968-03-01

Publication	Publication Date	Title
US5380518A (en)	1995-01-10	Method for the production of chlorine dioxide
US2894966A (en)	1959-07-14	Process for the preparation of stabilized organotitanium compounds
EP0692459A1 (de)	1996-01-17	Mittel zur Wasserbehandlung
US3702304A (en)	1972-11-07	Paint remover compositions
NO144071B (no)	1981-03-09	Analogifremgangsmaate ved fremstilling av antihypertensivt aktive thienyl- og thietyl-ureaer
GB2056991A (en)	1981-03-25	N - (hydroxymethyl) - aminoalkane-diphosphonic acids and their use as stabililizers in bleaching solutions
KR20010072712A (ko)	2001-07-31	수처리용 매질
US2988514A (en)	1961-06-13	Bleaching composition and method
US2430949A (en)	1947-11-18	Polyvinyl alcohol-stabilized ethanol formamide composition
JPH04265200A (ja)	1992-09-21	スケールの沈積を抑制する方法
US10995012B2 (en)	2021-05-04	Concentrated photoactive, neutral titanium dioxide sol
US20210204548A1 (en)	2021-07-08	Stabilized Biocide Composition
Kunigk et al.	2014	Influence of temperature and pH on the decomposition kinetics of peracetic acid in aqueous solutions
US1522561A (en)	1925-01-13	Bleaching solution
US2010615A (en)	1935-08-06	Production of anhydrous alkali metal hyposulphites
US2258578A (en)	1941-10-07	Acid inhibitor and noncorrosion acid liquor
US2154170A (en)	1939-04-11	Stable basic aluminum formate and solutions thereof
US3433590A (en)	1969-03-18	Dry stabilized alkali metal dithionite compositions
US2143478A (en)	1939-01-10	Manufacture of aliphatic tertiary alcohols
JPS60133074A (ja)	1985-07-16	ペイントストリツパー組成物
US2330452A (en)	1943-09-28	Method of making mercuric naphthenate
US992265A (en)	1911-05-16	Process of preserving hydrogen peroxid solution.
JPS621944B2 (de)	1987-01-16
US1126471A (en)	1915-01-26	Process of evaporation.
CN110650943B (zh)	2022-05-10	包含乳酸烷基酯的组合物