BE456086A - - Google Patents
Info
- Publication number
- BE456086A BE456086A BE456086DA BE456086A BE 456086 A BE456086 A BE 456086A BE 456086D A BE456086D A BE 456086DA BE 456086 A BE456086 A BE 456086A
- Authority
- BE
- Belgium
- Prior art keywords
- emi
- parts
- weight
- methylol
- polyamides
- Prior art date
Links
- 239000004952 Polyamide Substances 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 239000004902 Softening Agent Substances 0.000 claims description 5
- 229920002635 polyurethane Polymers 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 229920002396 Polyurea Polymers 0.000 claims description 3
- 238000009835 boiling Methods 0.000 claims description 3
- -1 methylol groups Chemical group 0.000 claims description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 150000001491 aromatic compounds Chemical class 0.000 description 3
- LBARXHIIOCOWOG-UHFFFAOYSA-N 1,2,3,4-tetrahydronaphthalen-1-ylmethanol Chemical compound C1=CC=C2C(CO)CCCC2=C1 LBARXHIIOCOWOG-UHFFFAOYSA-N 0.000 description 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- FEOMFFKZOZMBKD-UHFFFAOYSA-N (4-phenoxyphenyl)methanol Chemical compound C1=CC(CO)=CC=C1OC1=CC=CC=C1 FEOMFFKZOZMBKD-UHFFFAOYSA-N 0.000 description 1
- DMWVQPRNHLNVKL-UHFFFAOYSA-N [1-(hydroxymethyl)-3,4-dihydro-2h-naphthalen-1-yl]methanol Chemical compound C1=CC=C2C(CO)(CO)CCCC2=C1 DMWVQPRNHLNVKL-UHFFFAOYSA-N 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003763 resistance to breakage Effects 0.000 description 1
- 239000002904 solvent 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
- C08K5/04—Oxygen-containing compounds
- C08K5/05—Alcohols; Metal alcoholates
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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE904536X | 1943-06-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
BE456086A true BE456086A (OSRAM) |
Family
ID=6861898
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE456086D BE456086A (OSRAM) | 1943-06-03 |
Country Status (2)
Country | Link |
---|---|
BE (1) | BE456086A (OSRAM) |
FR (1) | FR904536A (OSRAM) |
-
0
- BE BE456086D patent/BE456086A/fr unknown
-
1944
- 1944-05-23 FR FR904536D patent/FR904536A/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
FR904536A (fr) | 1945-11-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Lindwall et al. | A condensation of Acetophenone with Isatin by the Knoevenagel Method1 | |
Grosheintz et al. | Synthesis of 6-nitro-6-desoxy-D-glucose and 6-nitro-6-desoxy-L-idose | |
BE456086A (OSRAM) | ||
Duff | 71. A new method for the preparation of p-dialkylaminobenzaldehydes | |
Hartman et al. | The preparation of Furil | |
Sullivan | The Preparation of L-Sorbose from Sorbitol by Chemical Methods | |
FR2465762A1 (fr) | Composition polymere thermoplastique apte au faconnage, contenant un acetal cyclique en tant qu'agent de nucleation | |
US2139121A (en) | Aliphatic nitroalcohols | |
Mosher et al. | Pentaphenylethanol | |
Kinney et al. | Dideuteriovaline and Dideuterioleucine | |
US1188014A (en) | Condensation product and method of preparing same. | |
Bachmann et al. | A New Synthesis of 4-Ketohexahydroindan | |
Kelkar et al. | VI. ESSENTIAL OIL FROM THE RHIZOMES OF ACORUS CALAMUS, LINN | |
Eccott et al. | CCLXXVII.—Investigations of the lower olefinic acids. Part I. n-Hexenoic acids | |
Schwenk et al. | Debromination of Mono and Dibromocholestanone | |
US2572563A (en) | Aromatic compositions and process of treating lactone material to prepare them | |
Ide et al. | 3-Methyl-3, 4-dihydroisoquinolines and 3-Methyl-1, 2, 3, 4-tetrahydroisoquinolines1 | |
US2666789A (en) | alpha, beta-(polyhydroxyaryl)-alkanamides and methods for their producton | |
US2176063A (en) | Derivatives of pyrazine carboxylic acid and processes for their production | |
BE624199A (OSRAM) | ||
US2813895A (en) | Purification of dehydroabietylamine | |
Hazlet et al. | The Bromination of 4-Phenylphenyl Chloroacetate | |
DE645880C (de) | Verfahren zur Herstellung von in p-Stellung zum Stickstoffatom durch die Aldehydgruppe substituierten heterocyclischen Stickstoffverbindungen | |
US762765A (en) | Homologues of isoionone and process of making same. | |
Ichikawa | STUDIES ON THE CONSTITUTION OF SHONANIC ACID, ONE OF THE TWO CHARACTERISTIC VOLATILE ACIDS FROM THE WOOD OF LIBOCEDRUS FORMOSANA, FLORIN. I. THE ISOLATION OF SHONANIC ACID AND ITS GENERAL PROPERTIES |