BE460922A - - Google Patents
Info
- Publication number
- BE460922A BE460922A BE460922DA BE460922A BE 460922 A BE460922 A BE 460922A BE 460922D A BE460922D A BE 460922DA BE 460922 A BE460922 A BE 460922A
- Authority
- BE
- Belgium
- Prior art keywords
- alcohols
- terpenes
- ethers
- salts
- sesquiterpenes
- Prior art date
Links
- 150000001298 alcohols Chemical class 0.000 claims description 10
- 150000003505 terpenes Chemical class 0.000 claims description 7
- 235000007586 terpenes Nutrition 0.000 claims description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 6
- 239000004014 plasticizer Substances 0.000 claims description 5
- 229930004725 sesquiterpene Natural products 0.000 claims description 5
- 150000004354 sesquiterpene derivatives Chemical class 0.000 claims description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 241001466538 Gymnogyps Species 0.000 claims 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 239000001856 Ethyl cellulose Substances 0.000 description 3
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 3
- 239000000020 Nitrocellulose Substances 0.000 description 3
- 229920001249 ethyl cellulose Polymers 0.000 description 3
- 235000019325 ethyl cellulose Nutrition 0.000 description 3
- 229920001220 nitrocellulos Polymers 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- -1 ethers salts Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229940049953 phenylacetate Drugs 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/01—Hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE460922A true BE460922A (index.php) |
Family
ID=113690
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE460922D BE460922A (index.php) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE460922A (index.php) |
-
0
- BE BE460922D patent/BE460922A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Brannock | Preparation of Sunstituted 4-Pentenals | |
| RO78862A (ro) | Compozitie insecticida si acaricida lichida | |
| CA2341574A1 (fr) | Phosphohalohydrines, procede de fabrication et applications | |
| BE460922A (index.php) | ||
| Balaban et al. | Reduction of pyrylium salts with sodium borohydride | |
| EP0588680A1 (fr) | Procédé pour l'isomérisation des oléfines. | |
| EP0696265A1 (fr) | Procede pour l'isomerisation des olefines | |
| US3375271A (en) | Sun-screening compounds | |
| JPH049388A (ja) | 含ケイ素α−シアノアクリレートの製造法 | |
| CA1296354C (fr) | 2,2-dimethyl 3-formyl cyclopropane carboxylate de pentafluoro-phenylmethyle, son procede de preparation et son application a la synthese de produits pesticides | |
| GB567807A (en) | Triphenylethylene derivatives | |
| KR960041303A (ko) | 점착제 조성물 및 그를 이용하는 점착테이프의 제조방법 | |
| CA1293089C (fr) | Polymeres capables d'absorber le rayonnement ultraviolet, leur preparation et leur application notamment en cosmetologie | |
| US1408423A (en) | Cellulose-ester composition | |
| Bish et al. | The reaction of imidazole with 2-phenyl, 4-chloromethylene-oxazol-5-one | |
| EP0021926B1 (fr) | Procédé de préparation d'alléthrolone optiquement active | |
| Traynham et al. | Effects of Ring Size on the Reactions of Cyclic Olefins: Halohydrins from METHYLENECYCLOALKANES1 | |
| DE749054C (de) | Verfahren zur Herstellung von ª‡-Cyanaethylalkylaethern | |
| US3459819A (en) | 8-chloro-1-octene | |
| US1994131A (en) | Process for the production of cineol | |
| CA2138881A1 (fr) | Procede d'isomerisation squelettale des olefines utilisant une matiere a base d'alumine | |
| Mundy et al. | Ring size effects. II. An examination of conditions for the pinacol rearrangement | |
| FR3157202B1 (fr) | Composition à base de robinine et de solvants hydrophiles | |
| BE575917A (index.php) | ||
| BE428751A (index.php) |