NO125932B - - Google Patents
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- Publication number
- NO125932B NO125932B NO150603A NO15060363A NO125932B NO 125932 B NO125932 B NO 125932B NO 150603 A NO150603 A NO 150603A NO 15060363 A NO15060363 A NO 15060363A NO 125932 B NO125932 B NO 125932B
- Authority
- NO
- Norway
- Prior art keywords
- mol
- formula
- crystals
- metal oxides
- ferromagnetic material
- Prior art date
Links
- 239000013078 crystal Substances 0.000 claims description 37
- 239000000203 mixture Substances 0.000 claims description 28
- 239000007795 chemical reaction product Substances 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 12
- 230000005294 ferromagnetic effect Effects 0.000 claims description 11
- 239000002184 metal Substances 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 229910044991 metal oxide Inorganic materials 0.000 claims description 10
- 150000004706 metal oxides Chemical class 0.000 claims description 10
- 239000003302 ferromagnetic material Substances 0.000 claims description 9
- 150000002739 metals Chemical class 0.000 claims description 8
- 229910052742 iron Inorganic materials 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 239000000463 material Substances 0.000 description 28
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 14
- 239000001301 oxygen Substances 0.000 description 14
- 229910052760 oxygen Inorganic materials 0.000 description 14
- 230000005415 magnetization Effects 0.000 description 13
- 230000035699 permeability Effects 0.000 description 13
- 238000005245 sintering Methods 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 9
- 239000011230 binding agent Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 238000001035 drying Methods 0.000 description 7
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
- 230000005291 magnetic effect Effects 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 229910000859 α-Fe Inorganic materials 0.000 description 6
- 229910052596 spinel Inorganic materials 0.000 description 5
- 239000011029 spinel Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 229910052788 barium Inorganic materials 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 102100026233 DAN domain family member 5 Human genes 0.000 description 3
- 101000912351 Homo sapiens DAN domain family member 5 Proteins 0.000 description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 229910052745 lead Inorganic materials 0.000 description 3
- 229910052712 strontium Inorganic materials 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 2
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229910001447 ferric ion Inorganic materials 0.000 description 2
- 229910001448 ferrous ion Inorganic materials 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000002269 spontaneous effect Effects 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 241000737241 Cocos Species 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Inorganic materials [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 244000240602 cacao Species 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000005307 ferromagnetism Effects 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000003891 oxalate salts Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Compounds Of Iron (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US233943A US3180862A (en) | 1962-10-29 | 1962-10-29 | Aryl sulfonic acid salts of alpha-aminobenzylpenicillins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO125932B true NO125932B (fi) | 1972-11-27 |
Family
ID=22879280
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO150603A NO125932B (fi) | 1962-10-29 | 1963-10-28 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3180862A (fi) |
| AT (1) | AT257041B (fi) |
| BR (1) | BR6354145D0 (fi) |
| CH (1) | CH457440A (fi) |
| DE (1) | DE1445506C3 (fi) |
| DK (1) | DK131907C (fi) |
| ES (1) | ES292978A1 (fi) |
| FI (1) | FI42330C (fi) |
| GB (1) | GB1007589A (fi) |
| NL (1) | NL140529B (fi) |
| NO (1) | NO125932B (fi) |
| SE (1) | SE317078B (fi) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1460440A (en) * | 1973-06-15 | 1977-01-06 | Glaxo Lab Ltd | Ampicillin anhydrate |
| US3271389A (en) * | 1963-03-21 | 1966-09-06 | Bristol Myers Co | Process for the isolation of certain basic penicillins |
| US3262928A (en) * | 1963-03-29 | 1966-07-26 | Bristol Myers Co | Process for the production of sodium alpha-aminobenzylpenicillin |
| US3278525A (en) * | 1964-06-08 | 1966-10-11 | Bristol Myers Co | Aminoaryldisulfonic acid salts of alpha-aminoarylmethylpenicillins |
| US3299046A (en) * | 1964-06-23 | 1967-01-17 | American Home Prod | Method of preparing anhydrous ampicillin |
| US3534035A (en) * | 1968-01-31 | 1970-10-13 | American Home Prod | Tetrahydronaphthalene sulfonic acid addition salt of ampicillin and process |
| US3676434A (en) * | 1970-07-29 | 1972-07-11 | Lilly Co Eli | Cephalosporin salts |
| NZ189945A (en) * | 1978-04-01 | 1981-04-24 | Beecham Group Ltd | Ampicillin phthalidyl ester naphthalene 2-sulphonate also pharmaceutical compositions |
| US4240960A (en) * | 1979-03-19 | 1980-12-23 | Bristol-Myers Company | Trimethylsilyl substituted penicillins |
| US4278600A (en) * | 1979-03-19 | 1981-07-14 | Bristol-Myers Company | Production of penicillins |
| US4310458A (en) * | 1979-03-19 | 1982-01-12 | Bristol-Myers Company | Production of penicillins |
| US4351766A (en) * | 1979-07-12 | 1982-09-28 | Bristol-Myers Company | Production of penicillins |
| IE51516B1 (en) * | 1980-10-06 | 1987-01-07 | Leo Pharm Prod Ltd | 1,1-dioxapenicillanoyloxymethyl 6-(d-alpha-amino-alpha-phenylacetamido)penicillanate napsylate |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2223935A (en) * | 1939-04-01 | 1940-12-03 | American Cyanamid Co | Amidine salts of alkyl naphthalene sulphonic acids |
| US2876236A (en) * | 1952-08-26 | 1959-03-03 | American Home Prod | Heterocyclic diamines and salts thereof |
| US2985648A (en) * | 1958-10-06 | 1961-05-23 | Doyle Frank Peter | Alpha-aminobenzylpenicillins |
| US3157640A (en) * | 1963-03-21 | 1964-11-17 | Bristol Myers Co | D-(-)-alpha-aminobenzylpenicillin trihydrate |
-
1962
- 1962-10-29 US US233943A patent/US3180862A/en not_active Expired - Lifetime
-
1963
- 1963-10-24 AT AT852263A patent/AT257041B/de active
- 1963-10-24 DE DE1445506A patent/DE1445506C3/de not_active Expired
- 1963-10-25 CH CH1312063A patent/CH457440A/de unknown
- 1963-10-26 DK DK505063A patent/DK131907C/da active
- 1963-10-28 GB GB42449/63A patent/GB1007589A/en not_active Expired
- 1963-10-28 SE SE11821/63A patent/SE317078B/xx unknown
- 1963-10-28 NO NO150603A patent/NO125932B/no unknown
- 1963-10-28 ES ES292978A patent/ES292978A1/es not_active Expired
- 1963-10-29 FI FI632115A patent/FI42330C/fi active
- 1963-10-29 NL NL63299854A patent/NL140529B/xx unknown
- 1963-10-29 BR BR154145/63A patent/BR6354145D0/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR6354145D0 (pt) | 1973-09-18 |
| DE1445506A1 (de) | 1969-10-09 |
| AT257041B (de) | 1967-09-25 |
| ES292978A1 (es) | 1964-03-16 |
| SE317078B (fi) | 1969-11-10 |
| NL140529B (nl) | 1973-12-17 |
| DE1445506B2 (de) | 1977-11-24 |
| DE1445506C3 (de) | 1978-07-20 |
| DK131907C (da) | 1976-02-23 |
| GB1007589A (en) | 1965-10-13 |
| US3180862A (en) | 1965-04-27 |
| CH457440A (de) | 1968-06-15 |
| FI42330C (fi) | 1970-07-10 |
| FI42330B (fi) | 1970-03-31 |
| DK131907B (da) | 1975-09-22 |
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