DK141475B - Fremgangsmåde til fremstilling af et dyrefoderadditiv indeholdende et antibiotikum AV290-syntankompleks. - Google Patents

Fremgangsmåde til fremstilling af et dyrefoderadditiv indeholdende et antibiotikum AV290-syntankompleks. Download PDF

Info

Publication number: DK141475B
Authority: DK; Denmark
Prior art keywords: antibiotic; synthane; complex; culture medium; preparation
Prior art date: 1970-11-03

Application number

DK530971AA

Other languages

Danish (da)

English (en)

Other versions

DK141475C (de

Inventor

Ping Shu

Murray Dann

Original Assignee

American Cyanamid Co

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.)

1970-11-03

Filing date

1971-10-29

Publication date

1980-03-24

1971-10-29 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

1980-03-24 Publication of DK141475B publication Critical patent/DK141475B/da

1980-08-25 Application granted granted Critical

1980-08-25 Publication of DK141475C publication Critical patent/DK141475C/da

Links

230000003115 biocidal effect Effects 0.000 title description 38
VGZTVHRJEVWFIA-UHFFFAOYSA-N synthane Chemical compound FC(F)OC(F)C(F)(F)C(F)F VGZTVHRJEVWFIA-UHFFFAOYSA-N 0.000 title description 19
238000000034 method Methods 0.000 title description 14
238000002360 preparation method Methods 0.000 title description 12
235000019730 animal feed additive Nutrition 0.000 title description 4
239000003242 anti bacterial agent Substances 0.000 title description 4
239000001963 growth medium Substances 0.000 description 23
239000000047 product Substances 0.000 description 17
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 14
239000007787 solid Substances 0.000 description 14
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
239000000203 mixture Substances 0.000 description 11
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 9
239000000243 solution Substances 0.000 description 7
235000013312 flour Nutrition 0.000 description 6
239000003674 animal food additive Substances 0.000 description 5
238000003756 stirring Methods 0.000 description 5
241000287828 Gallus gallus Species 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
240000008042 Zea mays Species 0.000 description 4
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
235000002017 Zea mays subsp mays Nutrition 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
235000013330 chicken meat Nutrition 0.000 description 4
235000005822 corn Nutrition 0.000 description 4
238000001914 filtration Methods 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
239000005909 Kieselgur Substances 0.000 description 3
AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 3
241000282849 Ruminantia Species 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
239000000969 carrier Substances 0.000 description 3
238000005119 centrifugation Methods 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
238000009833 condensation Methods 0.000 description 3
230000005494 condensation Effects 0.000 description 3
239000012065 filter cake Substances 0.000 description 3
239000002244 precipitate Substances 0.000 description 3
238000006277 sulfonation reaction Methods 0.000 description 3
238000012360 testing method Methods 0.000 description 3
GHOKWGTUZJEAQD-ZETCQYMHSA-N (D)-(+)-Pantothenic acid Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-ZETCQYMHSA-N 0.000 description 2
GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
229920001817 Agar Polymers 0.000 description 2
229930185605 Bisphenol Natural products 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
240000004658 Medicago sativa Species 0.000 description 2
235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
241000699670 Mus sp. Species 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
235000019742 Vitamins premix Nutrition 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000008272 agar Substances 0.000 description 2
229940088710 antibiotic agent Drugs 0.000 description 2
239000011260 aqueous acid Substances 0.000 description 2
-1 aromatic hydroxy compound Chemical class 0.000 description 2
150000001896 cresols Chemical class 0.000 description 2
238000010828 elution Methods 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical class O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 description 2
150000004780 naphthols Chemical class 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
244000144977 poultry Species 0.000 description 2
235000013594 poultry meat Nutrition 0.000 description 2
239000000843 powder Substances 0.000 description 2
230000002441 reversible effect Effects 0.000 description 2
238000001179 sorption measurement Methods 0.000 description 2
239000011573 trace mineral Substances 0.000 description 2
235000013619 trace mineral Nutrition 0.000 description 2
FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical class C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 description 1
FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
239000001763 2-hydroxyethyl(trimethyl)azanium Substances 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
239000004322 Butylated hydroxytoluene Substances 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 description 1
235000019743 Choline chloride Nutrition 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
241000252203 Clupea harengus Species 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
241000186216 Corynebacterium Species 0.000 description 1
AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
239000004470 DL Methionine Substances 0.000 description 1
235000019739 Dicalciumphosphate Nutrition 0.000 description 1
108010068370 Glutens Proteins 0.000 description 1
OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
235000019764 Soybean Meal Nutrition 0.000 description 1
241000187747 Streptomyces Species 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
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 description 1
241000282887 Suidae Species 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
229930003427 Vitamin E Natural products 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
238000007605 air drying Methods 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000037396 body weight Effects 0.000 description 1
229940036811 bone meal Drugs 0.000 description 1
239000002374 bone meal Substances 0.000 description 1
235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
229940095259 butylated hydroxytoluene Drugs 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000003610 charcoal Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
229960003178 choline chloride Drugs 0.000 description 1
SGMZJAMFUVOLNK-UHFFFAOYSA-M choline chloride Chemical compound [Cl-].C[N+](C)(C)CCO SGMZJAMFUVOLNK-UHFFFAOYSA-M 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
238000004440 column chromatography Methods 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000012343 cottonseed oil Nutrition 0.000 description 1
239000002385 cottonseed oil Substances 0.000 description 1
239000012531 culture fluid Substances 0.000 description 1
NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 description 1
229940038472 dicalcium phosphate Drugs 0.000 description 1
229910000390 dicalcium phosphate Inorganic materials 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000006052 feed supplement Substances 0.000 description 1
229960000304 folic acid Drugs 0.000 description 1
235000019152 folic acid Nutrition 0.000 description 1
239000011724 folic acid Substances 0.000 description 1
238000004108 freeze drying Methods 0.000 description 1
WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
238000007429 general method Methods 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
235000021312 gluten Nutrition 0.000 description 1
235000019514 herring Nutrition 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000010985 leather Substances 0.000 description 1
239000004571 lime Substances 0.000 description 1
235000021388 linseed oil Nutrition 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
229960004051 menadione sodium bisulfite Drugs 0.000 description 1
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 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
229930182817 methionine Natural products 0.000 description 1
FFEARJCKVFRZRR-UHFFFAOYSA-N methionine Chemical compound CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 description 1
235000006109 methionine Nutrition 0.000 description 1
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
235000013379 molasses Nutrition 0.000 description 1
239000000178 monomer Substances 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
229960003512 nicotinic acid Drugs 0.000 description 1
235000001968 nicotinic acid Nutrition 0.000 description 1
239000011664 nicotinic acid Substances 0.000 description 1
229940055726 pantothenic acid Drugs 0.000 description 1
235000019161 pantothenic acid Nutrition 0.000 description 1
239000011713 pantothenic acid Substances 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000006069 physical mixture Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
229960002477 riboflavin Drugs 0.000 description 1
235000019192 riboflavin Nutrition 0.000 description 1
239000002151 riboflavin Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
239000002195 soluble material Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000004455 soybean meal Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
229960004793 sucrose Drugs 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000041 toxicology testing Toxicity 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
235000019155 vitamin A Nutrition 0.000 description 1
239000011719 vitamin A Substances 0.000 description 1
MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
235000019165 vitamin E Nutrition 0.000 description 1
229940046009 vitamin E Drugs 0.000 description 1
239000011709 vitamin E Substances 0.000 description 1
229940045997 vitamin a Drugs 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G16/00—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
- C08G16/02—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
- C08G16/0212—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds
- C08G16/0218—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen
- C08G16/0237—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen containing sulfur
- 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
- A23K20/195—Antibiotics
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/18—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with phenols substituted by carboxylic or sulfonic acid groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/28—Chemically modified polycondensates

Landscapes

Chemical & Material Sciences (AREA)
Polymers & Plastics (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Husbandry (AREA)
General Chemical & Material Sciences (AREA)
Zoology (AREA)
Engineering & Computer Science (AREA)
Food Science & Technology (AREA)
Fodder In General (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Feed For Specific Animals (AREA)
Compounds Of Unknown Constitution (AREA)

DK530971AA 1970-11-03 1971-10-29 Fremgangsmåde til fremstilling af et dyrefoderadditiv indeholdende et antibiotikum AV290-syntankompleks. DK141475B (da)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US8660170A	1970-11-03	1970-11-03
US8660170		1970-11-03

Publications (2)

Publication Number	Publication Date
DK141475B true DK141475B (da)	1980-03-24
DK141475C DK141475C (de)	1980-08-25

Family

ID=22199652

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DK530971AA DK141475B (da)	1970-11-03	1971-10-29	Fremgangsmåde til fremstilling af et dyrefoderadditiv indeholdende et antibiotikum AV290-syntankompleks.

Country Status (22)

Country	Link
JP (1)	JPS551025B1 (de)
AR (1)	AR192327A1 (de)
AT (1)	AT324108B (de)
AU (1)	AU463112B2 (de)
BE (1)	BE774817A (de)
CA (1)	CA983015A (de)
CH (1)	CH554645A (de)
DE (1)	DE2154633C3 (de)
DK (1)	DK141475B (de)
ES (1)	ES396596A1 (de)
FR (1)	FR2113392A5 (de)
GB (1)	GB1323377A (de)
HU (1)	HU163819B (de)
IE (1)	IE35741B1 (de)
IL (1)	IL37978A (de)
IT (1)	IT1050190B (de)
MY (1)	MY7400223A (de)
NL (1)	NL167469C (de)
PH (1)	PH9247A (de)
SE (1)	SE378170B (de)
YU (1)	YU35953B (de)
ZA (1)	ZA716946B (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DD114342A5 (de) *	1973-04-27	1975-08-05
DE3005642A1 (de)	1980-02-15	1981-08-20	Hoechst Ag, 6000 Frankfurt	Feststoff der salinomycin-kulturbruehe und verfahren zu seiner gewinnung

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3338786A (en) *	1966-07-29	1967-08-29	American Cyanamid Co	Antibiotic av290 and production thereof

1971
- 1971-10-18 ZA ZA716946A patent/ZA716946B/xx unknown
- 1971-10-18 IE IE1305/71A patent/IE35741B1/xx unknown
- 1971-10-20 AU AU34788/71A patent/AU463112B2/en not_active Expired
- 1971-10-21 IL IL37978A patent/IL37978A/xx unknown
- 1971-10-22 PH PH12958*UA patent/PH9247A/en unknown
- 1971-10-25 GB GB4951871A patent/GB1323377A/en not_active Expired
- 1971-10-26 CA CA126,145A patent/CA983015A/en not_active Expired
- 1971-10-28 AR AR238729A patent/AR192327A1/es active
- 1971-10-29 FR FR7138954A patent/FR2113392A5/fr not_active Expired
- 1971-10-29 DK DK530971AA patent/DK141475B/da not_active IP Right Cessation
- 1971-11-02 SE SE7113955A patent/SE378170B/xx unknown
- 1971-11-02 IT IT53837/71A patent/IT1050190B/it active
- 1971-11-02 YU YU2772/71A patent/YU35953B/xx unknown
- 1971-11-02 HU HUAE344A patent/HU163819B/hu unknown
- 1971-11-03 AT AT946771A patent/AT324108B/de not_active IP Right Cessation
- 1971-11-03 DE DE2154633A patent/DE2154633C3/de not_active Expired
- 1971-11-03 ES ES396596A patent/ES396596A1/es not_active Expired
- 1971-11-03 NL NL7115137.A patent/NL167469C/xx not_active IP Right Cessation
- 1971-11-03 CH CH1602071A patent/CH554645A/de not_active IP Right Cessation
- 1971-11-03 BE BE774817A patent/BE774817A/xx not_active IP Right Cessation
- 1971-11-04 JP JP8796971A patent/JPS551025B1/ja active Pending
1974
- 1974-12-30 MY MY223/74A patent/MY7400223A/xx unknown

Also Published As

Publication number	Publication date
ZA716946B (en)	1972-06-28
AU3478871A (en)	1973-05-03
JPS551025B1 (de)	1980-01-11
MY7400223A (en)	1974-12-31
PH9247A (en)	1975-07-30
DE2154633A1 (de)	1972-05-04
BE774817A (fr)	1972-05-03
YU35953B (en)	1981-11-13
AU463112B2 (en)	1975-07-17
IE35741L (en)	1972-05-03
CA983015A (en)	1976-02-03
NL167469C (nl)	1981-12-16
YU277271A (en)	1981-04-30
AT324108B (de)	1975-08-11
NL7115137A (de)	1972-05-05
HU163819B (de)	1973-11-28
IL37978A0 (en)	1971-12-29
DE2154633B2 (de)	1981-07-30
IE35741B1 (en)	1976-05-12
DE2154633C3 (de)	1982-04-29
GB1323377A (en)	1973-07-11
IT1050190B (it)	1981-03-10
SE378170B (de)	1975-08-25
DK141475C (de)	1980-08-25
AR192327A1 (es)	1973-02-14
NL167469B (nl)	1981-07-16
ES396596A1 (es)	1974-12-16
CH554645A (de)	1974-10-15
IL37978A (en)	1974-05-16
FR2113392A5 (de)	1972-06-23

Legal Events

Date	Code	Title	Description
1991-12-16	PUP	Patent expired

Publication	Publication Date	Title
Martin‐Tanguy et al.	1977	Condensed tannins in horse bean seeds: chemical structure and apparent effects on poultry
NO143509B (no)	1980-11-17	Regulerbar rulleunderstoettelse for en roterende trommel
GB2037306A (en)	1980-07-09	Cyclodextrin-camomile inclusion complexes and pharmaceutical compositions containing them
WO2013171371A1 (en)	2013-11-21	Use of saponified tall oil fatty acid
SU1047377A3 (ru)	1983-10-07	Способ получени кормовой добавки на основе антибиотика @ 290
US4804536A (en)	1989-02-14	Dietary fibres of seaweed having ion-exchange ability
DE2154633C3 (de)	1982-04-29	Tierfutterzusatz und Verfahren zu seiner Herstellung
US4196199A (en)	1980-04-01	Antibiotic BM123 syntan complexes
Dewar et al.	1971	Sodium toxicity resulting from feeding hen egg albumen powder to turkey poults
EP0003644A1 (de)	1979-08-22	Tierfutterzusätze die ein Antibiotikum trans-BM 123-Gamma enthalten und Verfahren zu deren Herstellung
US4291026A (en)	1981-09-22	Antibiotic BM123ν pamoate complexes
US4141974A (en)	1979-02-27	Veterinary method employing certain aureolic acid compounds
US4196198A (en)	1980-04-01	Antibiotic BM123-alkyl sulfate complexes
US3950515A (en)	1976-04-13	Animal feeds containing antibiotic AV290
US2861025A (en)	1958-11-18	Process for obtaining vitamin b12 and vitamin b12-like substances and the products thereof
Bray et al.	1965	The effects of early and late maturity on the protein requirements of pullets
US4237120A (en)	1980-12-02	Antibacterial agent BM123-gamma, pharmaceutically acceptable salts, complexes and alkylated derivatives as animal food additives
CN103271226A (zh)	2013-09-04	一种低二噁英含量的辣椒红饲料添加剂的制备方法
US3266901A (en)	1966-08-16	Feed containing nocardia rugosa free from vitamin b12
DE3028594C2 (de)	1987-10-15
GB752552A (en)	1956-07-11	Improvements in and relating to growth factors
Jackson	1971	Composition of feather and offal meal and its value as a protein supplement in the diet of caged laying hens
DE2140322A1 (de)	1972-02-17	Neues Antibiotikum
Arnaudov et al.	2020	study on some hematological and blood biochemical parameters of newly introduced layer breeds depending on the laying period
SU730274A3 (ru)	1980-04-25	Способ усилени роста животных и птиц