DE2645715A1 - Furan- und thiophenderivate als konservierungsstoffe und silierhilfsmittel - Google Patents
Furan- und thiophenderivate als konservierungsstoffe und silierhilfsmittelInfo
- Publication number
- DE2645715A1 DE2645715A1 DE19762645715 DE2645715A DE2645715A1 DE 2645715 A1 DE2645715 A1 DE 2645715A1 DE 19762645715 DE19762645715 DE 19762645715 DE 2645715 A DE2645715 A DE 2645715A DE 2645715 A1 DE2645715 A1 DE 2645715A1
- Authority
- DE
- Germany
- Prior art keywords
- feed
- furan
- preservation
- thiophene
- acid
- 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.)
- Withdrawn
Links
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 title claims description 20
- 239000003755 preservative agent Substances 0.000 title claims description 11
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical class C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 title description 2
- 239000000126 substance Substances 0.000 claims description 9
- 238000004321 preservation Methods 0.000 claims description 7
- 230000002335 preservative effect Effects 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 150000003577 thiophenes Chemical class 0.000 claims description 4
- 239000011573 trace mineral Substances 0.000 claims description 3
- 235000013619 trace mineral Nutrition 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 235000019728 animal nutrition Nutrition 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 230000009286 beneficial effect Effects 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 235000010755 mineral Nutrition 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 1
- 230000000694 effects Effects 0.000 description 11
- 239000002253 acid Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 241000209140 Triticum Species 0.000 description 7
- 235000021307 Triticum Nutrition 0.000 description 7
- 206010061217 Infestation Diseases 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- -1 thiophene aldehydes Chemical class 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 235000013339 cereals Nutrition 0.000 description 4
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 4
- RBIGKSZIQCTIJF-UHFFFAOYSA-N 3-formylthiophene Chemical compound O=CC=1C=CSC=1 RBIGKSZIQCTIJF-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- IHCCAYCGZOLTEU-UHFFFAOYSA-N Furane-3-carboxylic acid Natural products OC(=O)C=1C=COC=1 IHCCAYCGZOLTEU-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- CNUDBTRUORMMPA-UHFFFAOYSA-N formylthiophene Chemical compound O=CC1=CC=CS1 CNUDBTRUORMMPA-UHFFFAOYSA-N 0.000 description 3
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- QERYCTSHXKAMIS-UHFFFAOYSA-N thiophene-2-carboxylic acid Chemical class OC(=O)C1=CC=CS1 QERYCTSHXKAMIS-UHFFFAOYSA-N 0.000 description 3
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical compound OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 description 2
- OUDFNZMQXZILJD-UHFFFAOYSA-N 5-methyl-2-furaldehyde Chemical compound CC1=CC=C(C=O)O1 OUDFNZMQXZILJD-UHFFFAOYSA-N 0.000 description 2
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- WAEMQWOKJMHJLA-UHFFFAOYSA-N Manganese(2+) Chemical compound [Mn+2] WAEMQWOKJMHJLA-UHFFFAOYSA-N 0.000 description 2
- 240000004658 Medicago sativa Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 229960004365 benzoic acid Drugs 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000004312 hexamethylene tetramine Substances 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 235000009973 maize Nutrition 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZIXGKVIXATUKLG-UHFFFAOYSA-N 3,4,5-trimethyl-2h-furan-3-carboxylic acid Chemical compound CC1=C(C)C(C)(C(O)=O)CO1 ZIXGKVIXATUKLG-UHFFFAOYSA-N 0.000 description 1
- ANIABPZLKNMRLN-UHFFFAOYSA-N 3-ethylthiophene-2-carbaldehyde Chemical compound CCC=1C=CSC=1C=O ANIABPZLKNMRLN-UHFFFAOYSA-N 0.000 description 1
- BSQKBHXYEKVKMN-UHFFFAOYSA-N 3-methylthiophene-2-carbaldehyde Chemical compound CC=1C=CSC=1C=O BSQKBHXYEKVKMN-UHFFFAOYSA-N 0.000 description 1
- CONLQGNBFRQUBX-UHFFFAOYSA-N 3-thiophen-2-ylprop-2-enenitrile Chemical compound N#CC=CC1=CC=CS1 CONLQGNBFRQUBX-UHFFFAOYSA-N 0.000 description 1
- CBHZBVLWQJCTQF-UHFFFAOYSA-N 3-thiophen-3-ylprop-2-enenitrile Chemical compound N#CC=CC=1C=CSC=1 CBHZBVLWQJCTQF-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- VAUMDUIUEPIGHM-UHFFFAOYSA-N 5-Methyl-2-thiophenecarboxaldehyde Chemical compound CC1=CC=C(C=O)S1 VAUMDUIUEPIGHM-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 244000075850 Avena orientalis Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 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 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 241000209056 Secale Species 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241000219793 Trifolium Species 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 235000021120 animal protein Nutrition 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000003385 bacteriostatic effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 1
- 229910000001 cobalt(II) carbonate Inorganic materials 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229940013688 formic acid Drugs 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- SYLAFCZSYRXBJF-UHFFFAOYSA-N furan-3,4-dicarboxylic acid Chemical compound OC(=O)C1=COC=C1C(O)=O SYLAFCZSYRXBJF-UHFFFAOYSA-N 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000000622 irritating effect Effects 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229960000448 lactic acid Drugs 0.000 description 1
- 235000021374 legumes Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229940095574 propionic acid Drugs 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011973 solid acid Substances 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- GSXCEVHRIVLFJV-UHFFFAOYSA-N thiophene-3-carbonitrile Chemical compound N#CC=1C=CSC=1 GSXCEVHRIVLFJV-UHFFFAOYSA-N 0.000 description 1
- YNVOMSDITJMNET-UHFFFAOYSA-N thiophene-3-carboxylic acid Chemical compound OC(=O)C=1C=CSC=1 YNVOMSDITJMNET-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K30/00—Processes specially adapted for preservation of materials in order to produce animal feeding-stuffs
- A23K30/10—Processes specially adapted for preservation of materials in order to produce animal feeding-stuffs of green fodder
- A23K30/15—Processes specially adapted for preservation of materials in order to produce animal feeding-stuffs of green fodder using chemicals or microorganisms for ensilaging
-
- 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
- A23K20/116—Heterocyclic compounds
- A23K20/121—Heterocyclic compounds containing oxygen or sulfur as hetero atom
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K30/00—Processes specially adapted for preservation of materials in order to produce animal feeding-stuffs
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Animal Husbandry (AREA)
- Zoology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Meat, Egg Or Seafood Products (AREA)
- General Preparation And Processing Of Foods (AREA)
- Fodder In General (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762645715 DE2645715A1 (de) | 1976-10-09 | 1976-10-09 | Furan- und thiophenderivate als konservierungsstoffe und silierhilfsmittel |
| FI772471A FI60106C (fi) | 1976-10-09 | 1977-08-18 | Foerfarande foer konservering av fodermedel genom anvaendning av furan- eller tiofenderivat |
| JP11008177A JPS5348886A (en) | 1976-10-09 | 1977-09-14 | Furan as rreservative and reserve auxiliary agent and thiophene derivatives and method of preserving feed therewith |
| US05/834,419 US4139641A (en) | 1976-10-09 | 1977-09-19 | Furan and thiophene derivatives as preservatives and silage conditioners |
| BE181196A BE859049A (fr) | 1976-10-09 | 1977-09-26 | Agents de conservation et de silotage pour les fourrages a base de derive du furanne et du thiophene |
| CH1224477A CH633417A5 (de) | 1976-10-09 | 1977-10-06 | Mittel zum konservieren von futtermitteln. |
| HU77BA3592A HU177547B (en) | 1976-10-09 | 1977-10-07 | Process for canning fodder with furane- or thiophene derivatives |
| AT716777A AT353593B (de) | 1976-10-09 | 1977-10-07 | Verfahren zur konservierung von futtermitteln |
| FR7730294A FR2366802A1 (fr) | 1976-10-09 | 1977-10-07 | Derives de furanne et de thiophene comme agents de conservation et d'ensilage |
| NL7711056A NL7711056A (nl) | 1976-10-09 | 1977-10-07 | Werkwijze voor de bereiding van een preparaat voor het conserveren en in kuilen opslaan van voer. |
| NO773433A NO145559C (no) | 1976-10-09 | 1977-10-07 | Konservert forstoff |
| GB41779/77A GB1588329A (en) | 1976-10-09 | 1977-10-07 | Furan and thiophene derivatives as preservatives for animal feedstuffs and silage conditioners |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762645715 DE2645715A1 (de) | 1976-10-09 | 1976-10-09 | Furan- und thiophenderivate als konservierungsstoffe und silierhilfsmittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2645715A1 true DE2645715A1 (de) | 1978-04-13 |
Family
ID=5990114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19762645715 Withdrawn DE2645715A1 (de) | 1976-10-09 | 1976-10-09 | Furan- und thiophenderivate als konservierungsstoffe und silierhilfsmittel |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4139641A (enExample) |
| JP (1) | JPS5348886A (enExample) |
| AT (1) | AT353593B (enExample) |
| BE (1) | BE859049A (enExample) |
| CH (1) | CH633417A5 (enExample) |
| DE (1) | DE2645715A1 (enExample) |
| FI (1) | FI60106C (enExample) |
| FR (1) | FR2366802A1 (enExample) |
| GB (1) | GB1588329A (enExample) |
| HU (1) | HU177547B (enExample) |
| NL (1) | NL7711056A (enExample) |
| NO (1) | NO145559C (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4617047A (en) * | 1982-07-27 | 1986-10-14 | Campbell Soup Company | Mushroom supplement |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE285726C (enExample) * | ||||
| GB479437A (en) * | 1935-08-12 | 1938-02-04 | Int Suiker En Alcohol Cie Inte | An improved method of stabilizing green fodder |
| US2527372A (en) * | 1948-02-25 | 1950-10-24 | Dow Chemical Co | Diphenyl halo-thiophene and fungicidal compositions containing the same |
| US3031447A (en) * | 1959-03-18 | 1962-04-24 | Masajiro Ueno | New nitrofuranacrylic derivatives |
| DE1176982B (de) * | 1960-03-16 | 1964-08-27 | Joseph Frateur | Mittel zur Silierung von Futterstoffen |
| FR1290405A (fr) * | 1961-03-31 | 1962-04-13 | Commercial Solvents Corp | Procédé de conservation du fourrage |
| FR1367878A (fr) * | 1962-11-03 | 1964-07-24 | Merck Ag E | Agent conservateur |
| FR1350241A (fr) * | 1963-02-18 | 1964-01-24 | Kaken Kagaku Kk | Procédé pour la maturation des produits d'ensilage |
| FR1458540A (fr) * | 1965-09-27 | 1966-03-04 | Centre Nat Rech Scient | Composés acryliques soufrés et leur préparation |
| DE1793471A1 (de) * | 1968-09-23 | 1971-07-01 | Hoechst Ag | Thiophen-3-isonitrile und Verfahren zu ihrer Herstellung |
| DE2412801A1 (de) * | 1974-03-16 | 1975-09-18 | Degussa | Konservierungsstoffe fuer futtermittel und mischfutter |
| US4010165A (en) * | 1974-10-03 | 1977-03-01 | Basf Aktiengesellschaft | Manufacture of thiophen-3-aldehyde |
-
1976
- 1976-10-09 DE DE19762645715 patent/DE2645715A1/de not_active Withdrawn
-
1977
- 1977-08-18 FI FI772471A patent/FI60106C/fi not_active IP Right Cessation
- 1977-09-14 JP JP11008177A patent/JPS5348886A/ja active Pending
- 1977-09-19 US US05/834,419 patent/US4139641A/en not_active Expired - Lifetime
- 1977-09-26 BE BE181196A patent/BE859049A/xx not_active IP Right Cessation
- 1977-10-06 CH CH1224477A patent/CH633417A5/de not_active IP Right Cessation
- 1977-10-07 NO NO773433A patent/NO145559C/no unknown
- 1977-10-07 GB GB41779/77A patent/GB1588329A/en not_active Expired
- 1977-10-07 AT AT716777A patent/AT353593B/de not_active IP Right Cessation
- 1977-10-07 FR FR7730294A patent/FR2366802A1/fr active Granted
- 1977-10-07 HU HU77BA3592A patent/HU177547B/hu unknown
- 1977-10-07 NL NL7711056A patent/NL7711056A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FI60106C (fi) | 1981-12-10 |
| JPS5348886A (en) | 1978-05-02 |
| US4139641A (en) | 1979-02-13 |
| NO773433L (no) | 1978-04-11 |
| AT353593B (de) | 1979-11-26 |
| FR2366802B1 (enExample) | 1984-01-27 |
| FI60106B (fi) | 1981-08-31 |
| FR2366802A1 (fr) | 1978-05-05 |
| NL7711056A (nl) | 1978-04-11 |
| NO145559B (no) | 1982-01-11 |
| ATA716777A (de) | 1979-04-15 |
| NO145559C (no) | 1982-04-21 |
| GB1588329A (en) | 1981-04-23 |
| HU177547B (en) | 1981-11-28 |
| BE859049A (fr) | 1978-03-28 |
| FI772471A7 (fi) | 1978-04-10 |
| CH633417A5 (de) | 1982-12-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8130 | Withdrawal |