DK2804940T3 - APPLICATION OF IMPROVED N-ALKYL-PYRROLIDON SOLVENTS - Google Patents
APPLICATION OF IMPROVED N-ALKYL-PYRROLIDON SOLVENTS Download PDFInfo
- Publication number
- DK2804940T3 DK2804940T3 DK13703739.6T DK13703739T DK2804940T3 DK 2804940 T3 DK2804940 T3 DK 2804940T3 DK 13703739 T DK13703739 T DK 13703739T DK 2804940 T3 DK2804940 T3 DK 2804940T3
- Authority
- DK
- Denmark
- Prior art keywords
- solvent
- butylpyrrolidone
- nmp
- agent
- pyrrolidone
- Prior art date
Links
- 239000002904 solvent Substances 0.000 title claims description 115
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 90
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 73
- BNXZHVUCNYMNOS-UHFFFAOYSA-N 1-butylpyrrolidin-2-one Chemical compound CCCCN1CCCC1=O BNXZHVUCNYMNOS-UHFFFAOYSA-N 0.000 claims description 52
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 claims description 38
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 24
- 239000003795 chemical substances by application Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 11
- -1 polytetrafluoroethylene Polymers 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 11
- VATRWWPJWVCZTA-UHFFFAOYSA-N 3-oxo-n-[2-(trifluoromethyl)phenyl]butanamide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1C(F)(F)F VATRWWPJWVCZTA-UHFFFAOYSA-N 0.000 claims description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 9
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 8
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 claims description 8
- 239000003973 paint Substances 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 claims description 6
- 238000009472 formulation Methods 0.000 claims description 6
- FILVIKOEJGORQS-UHFFFAOYSA-N 1,5-dimethylpyrrolidin-2-one Chemical compound CC1CCC(=O)N1C FILVIKOEJGORQS-UHFFFAOYSA-N 0.000 claims description 5
- 239000004793 Polystyrene Substances 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 239000003905 agrochemical Substances 0.000 claims description 4
- 238000002485 combustion reaction Methods 0.000 claims description 4
- 239000002285 corn oil Substances 0.000 claims description 4
- 235000005687 corn oil Nutrition 0.000 claims description 4
- 239000006184 cosolvent Substances 0.000 claims description 4
- 229940116333 ethyl lactate Drugs 0.000 claims description 4
- WEFZXWJJPHGTTN-UHFFFAOYSA-N methyl 5-(dimethylamino)-2-methyl-5-oxopentanoate Chemical compound COC(=O)C(C)CCC(=O)N(C)C WEFZXWJJPHGTTN-UHFFFAOYSA-N 0.000 claims description 4
- 239000004814 polyurethane Substances 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229920002554 vinyl polymer Polymers 0.000 claims description 4
- 229920002678 cellulose Polymers 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 239000012459 cleaning agent Substances 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- 230000008021 deposition Effects 0.000 claims description 3
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 150000004702 methyl esters Chemical class 0.000 claims description 3
- 238000004377 microelectronic Methods 0.000 claims description 3
- 229920002120 photoresistant polymer Polymers 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 3
- 229920002635 polyurethane Polymers 0.000 claims description 3
- 239000004800 polyvinyl chloride Substances 0.000 claims description 3
- 238000009987 spinning Methods 0.000 claims description 3
- 125000006091 1,3-dioxolane group Chemical class 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 239000004642 Polyimide Substances 0.000 claims description 2
- 239000000356 contaminant Substances 0.000 claims description 2
- 239000013527 degreasing agent Substances 0.000 claims description 2
- 238000005237 degreasing agent Methods 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 238000001125 extrusion Methods 0.000 claims description 2
- 238000010030 laminating Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 229920002492 poly(sulfone) Polymers 0.000 claims description 2
- 229920002239 polyacrylonitrile Polymers 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 229920001721 polyimide Polymers 0.000 claims description 2
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 2
- 239000011118 polyvinyl acetate Substances 0.000 claims description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 2
- 239000002966 varnish Substances 0.000 claims description 2
- 239000003085 diluting agent Substances 0.000 claims 6
- 239000002270 dispersing agent Substances 0.000 claims 6
- 230000002745 absorbent Effects 0.000 claims 5
- 239000002250 absorbent Substances 0.000 claims 5
- 239000012429 reaction media Substances 0.000 claims 3
- 239000003549 soybean oil Substances 0.000 claims 2
- 235000012424 soybean oil Nutrition 0.000 claims 2
- WOZTTWIULNULHG-UHFFFAOYSA-N 2,4,6-trioxabicyclo[3.1.0]hexane Chemical compound C1OC2C(O1)O2 WOZTTWIULNULHG-UHFFFAOYSA-N 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- 239000004922 lacquer Substances 0.000 claims 1
- 238000009740 moulding (composite fabrication) Methods 0.000 claims 1
- 229920003055 poly(ester-imide) Polymers 0.000 claims 1
- 231100000091 reproductive toxicant Toxicity 0.000 claims 1
- 238000009991 scouring Methods 0.000 claims 1
- 238000012360 testing method Methods 0.000 description 30
- 230000037396 body weight Effects 0.000 description 25
- 150000001875 compounds Chemical class 0.000 description 24
- 235000019786 weight gain Nutrition 0.000 description 13
- 235000012631 food intake Nutrition 0.000 description 11
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 10
- 231100001260 reprotoxic Toxicity 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 239000004962 Polyamide-imide Substances 0.000 description 7
- 229920002312 polyamide-imide Polymers 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- DCALJVULAGICIX-UHFFFAOYSA-N 1-propylpyrrolidin-2-one Chemical compound CCCN1CCCC1=O DCALJVULAGICIX-UHFFFAOYSA-N 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 5
- 239000010949 copper Substances 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 230000013011 mating Effects 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000004040 pyrrolidinones Chemical class 0.000 description 5
- 239000011877 solvent mixture Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 4
- 210000003298 dental enamel Anatomy 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000018109 developmental process Effects 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 4
- 210000000614 rib Anatomy 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 244000068988 Glycine max Species 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 3
- 231100000303 OECD 422 Combined Repeated Dose Toxicity Study with the Reproduction/Developmental Toxicity Screening Test Toxicity 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 210000000845 cartilage Anatomy 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 229940113088 dimethylacetamide Drugs 0.000 description 3
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 210000000216 zygoma Anatomy 0.000 description 3
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 description 2
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 2
- IVUYGANTXQVDDG-UHFFFAOYSA-N 1-(2-methylpropyl)pyrrolidin-2-one Chemical compound CC(C)CN1CCCC1=O IVUYGANTXQVDDG-UHFFFAOYSA-N 0.000 description 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 2
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 2
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 2
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 239000005877 Alpha-Cypermethrin Substances 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 239000005944 Chlorpyrifos Substances 0.000 description 2
- 239000005760 Difenoconazole Substances 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 238000011887 Necropsy Methods 0.000 description 2
- 239000005590 Oxyfluorfen Substances 0.000 description 2
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 description 2
- 239000005591 Pendimethalin Substances 0.000 description 2
- 239000005594 Phenmedipham Substances 0.000 description 2
- 241000700157 Rattus norvegicus Species 0.000 description 2
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 2
- 239000005839 Tebuconazole Substances 0.000 description 2
- 239000005846 Triadimenol Substances 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 210000000854 cervical rib Anatomy 0.000 description 2
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000002761 deinking Substances 0.000 description 2
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000035558 fertility Effects 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 238000002513 implantation Methods 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 description 2
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 2
- IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 229920003009 polyurethane dispersion Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 231100000191 repeated dose toxicity Toxicity 0.000 description 2
- 238000001542 size-exclusion chromatography Methods 0.000 description 2
- 210000003625 skull Anatomy 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 230000002110 toxicologic effect Effects 0.000 description 2
- 231100000723 toxicological property Toxicity 0.000 description 2
- 231100000041 toxicology testing Toxicity 0.000 description 2
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 2
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 2
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 2
- PKGXVWBTRTVHDW-UHFFFAOYSA-N 1-(6-methylheptyl)pyrrolidin-2-one Chemical compound CC(C)CCCCCN1CCCC1=O PKGXVWBTRTVHDW-UHFFFAOYSA-N 0.000 description 1
- GVDQKJQFVPXADH-UHFFFAOYSA-N 1-propan-2-ylpiperidin-2-one Chemical compound CC(C)N1CCCCC1=O GVDQKJQFVPXADH-UHFFFAOYSA-N 0.000 description 1
- LUVQSCCABURXJL-UHFFFAOYSA-N 1-tert-butylpyrrolidin-2-one Chemical compound CC(C)(C)N1CCCC1=O LUVQSCCABURXJL-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 1
- WPPOGHDFAVQKLN-UHFFFAOYSA-N N-Octyl-2-pyrrolidone Chemical compound CCCCCCCCN1CCCC1=O WPPOGHDFAVQKLN-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 206010074268 Reproductive toxicity Diseases 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000013475 authorization Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000005810 carbonylation reaction Methods 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 229920006334 epoxy coating Polymers 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000000895 extractive distillation Methods 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000003682 fluorination reaction Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000003304 gavage Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 210000002149 gonad Anatomy 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 230000008821 health effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 231100000092 inhalation hazard Toxicity 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229910001416 lithium ion Inorganic materials 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 210000001161 mammalian embryo Anatomy 0.000 description 1
- 230000008774 maternal effect Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000011164 ossification Effects 0.000 description 1
- 239000010893 paper waste Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- WEXRUCMBJFQVBZ-UHFFFAOYSA-N pentobarbital Chemical compound CCCC(C)C1(CC)C(=O)NC(=O)NC1=O WEXRUCMBJFQVBZ-UHFFFAOYSA-N 0.000 description 1
- 229960001412 pentobarbital Drugs 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000011527 polyurethane coating Substances 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000007696 reproductive toxicity Effects 0.000 description 1
- 231100000372 reproductive toxicity Toxicity 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000012488 skeletal system development Effects 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 230000021595 spermatogenesis Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000010254 subcutaneous injection Methods 0.000 description 1
- 239000007929 subcutaneous injection Substances 0.000 description 1
- 231100000615 substance of very high concern Toxicity 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000048 toxicity data Toxicity 0.000 description 1
- 231100000440 toxicity profile Toxicity 0.000 description 1
- 231100000583 toxicological profile Toxicity 0.000 description 1
- 210000004291 uterus Anatomy 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/12—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C09D127/18—Homopolymers or copolymers of tetrafluoroethene
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D179/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
- C09D179/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C09D179/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3281—Heterocyclic compounds
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
- C11D7/5013—Organic solvents containing nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Toxicology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Detergent Compositions (AREA)
- Pyrrole Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Paints Or Removers (AREA)
- Exposure Of Semiconductors, Excluding Electron Or Ion Beam Exposure (AREA)
- Cleaning Or Drying Semiconductors (AREA)
- Cleaning By Liquid Or Steam (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE2012/0037A BE1020269A5 (nl) | 2012-01-17 | 2012-01-17 | Gebruik van vervangende oplosmiddelen voor n-methylpyrrolidon (nmp). |
| PCT/EP2013/050852 WO2013107822A1 (en) | 2012-01-17 | 2013-01-17 | Use of improved n-alkyl pyrrolidone solvents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DK2804940T3 true DK2804940T3 (en) | 2018-11-05 |
Family
ID=47710093
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DK13703739.6T DK2804940T3 (en) | 2012-01-17 | 2013-01-17 | APPLICATION OF IMPROVED N-ALKYL-PYRROLIDON SOLVENTS |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20150057375A1 (enExample) |
| EP (1) | EP2804940B1 (enExample) |
| JP (2) | JP2015511935A (enExample) |
| KR (1) | KR101515848B1 (enExample) |
| CN (1) | CN104136595A (enExample) |
| BE (1) | BE1020269A5 (enExample) |
| CA (1) | CA2861145C (enExample) |
| DK (1) | DK2804940T3 (enExample) |
| ES (1) | ES2691268T3 (enExample) |
| IN (1) | IN2014DN06843A (enExample) |
| MX (1) | MX363336B (enExample) |
| PL (1) | PL2804940T3 (enExample) |
| WO (1) | WO2013107822A1 (enExample) |
Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE1020269A5 (nl) * | 2012-01-17 | 2013-07-02 | Taminco | Gebruik van vervangende oplosmiddelen voor n-methylpyrrolidon (nmp). |
| JP5990928B2 (ja) * | 2012-02-24 | 2016-09-14 | Jsr株式会社 | 液晶配向剤 |
| WO2015051928A1 (en) * | 2013-10-11 | 2015-04-16 | Solvay Specialty Polymers Italy S.P.A. | Process for manufacturing fluoropolymer membranes |
| US9725617B2 (en) * | 2014-04-17 | 2017-08-08 | Fujifilm Hunt Chemicals U.S.A., Inc. | Low toxicity solvent system for polyamideimide and polyamide amic acid resin coating |
| US9815941B2 (en) * | 2014-04-17 | 2017-11-14 | Cymer-Dayton, Llc | Low toxicity solvent system for polyamdieimide and polyamide amic acid resin manufacture |
| US20160024320A1 (en) * | 2014-07-24 | 2016-01-28 | Kolazi S. Narayanan | Mixed solvent based compositions for removal of paint and varnish |
| CN104152307B (zh) * | 2014-08-08 | 2017-11-10 | 深圳市爱康泉水处理服务有限公司 | 一种清洗剂用组合物和清洗剂及其应用 |
| US20160208097A1 (en) | 2015-01-15 | 2016-07-21 | Rohm And Haas Electronic Materials Llc | Polyimide compositions and methods |
| WO2016124251A1 (en) * | 2015-02-06 | 2016-08-11 | Taminco | Aqueous polyurethane dispersions |
| FR3040997B1 (fr) * | 2015-09-15 | 2019-12-27 | Arkema France | Composition de solvant(s) comprenant un melange d'une molecule ayant une fonction sulfoxyde et d'une molecule ayant une fonction amide |
| FR3040995B1 (fr) | 2015-09-15 | 2019-12-27 | Arkema France | Utilisation de composes comprenant une fonction sulfoxyde ou sulfone et une fonction amide comme solvants et nouveaux solvants |
| FR3041357B1 (fr) * | 2015-09-17 | 2017-09-01 | Rhodia Operations | Solvants de decapage des resines photosensibles |
| CN105695150A (zh) * | 2016-03-22 | 2016-06-22 | 深圳市盛元半导体有限公司 | 一种led封装残胶的除胶剂 |
| JP6878752B2 (ja) * | 2016-05-23 | 2021-06-02 | 学校法人神奈川大学 | フレキシブル熱電変換部材の作製方法 |
| DE102016210164A1 (de) | 2016-06-08 | 2017-12-14 | Clariant International Ltd | Verwendung von N-substituierten Pyrrolidonen zur Förderung der Penetration von agrochemischen Wirkstoffen |
| SE540725C2 (en) * | 2016-06-23 | 2018-10-23 | Ohla Plast & Faergteknik Ab | Use of composition comprising polyvinyl chloride dissolved in1-bytylpyrrolidin-2-one for joining floor panels made of po lyvinyl chloride |
| PL3287477T3 (pl) * | 2016-08-24 | 2020-01-31 | Henkel Ag & Co. Kgaa | Wspomaganie adhezji tworzywa sztucznego w poliuretanowych środkach adhezyjnych 2K |
| CN106752893A (zh) * | 2016-12-16 | 2017-05-31 | 吴中区穹窿山福顺生物技术研究所 | 一种电缆用耐腐蚀漆包线漆及其制备方法 |
| KR101921553B1 (ko) * | 2016-12-29 | 2018-11-26 | 코오롱글로텍주식회사 | 친환경 폴리우레탄수지 희석제 및 세척제 |
| WO2018162554A1 (en) * | 2017-03-09 | 2018-09-13 | Basf Se | Biodegradable solvent |
| KR101899098B1 (ko) * | 2017-04-28 | 2018-09-14 | 지에스칼텍스 주식회사 | 폴리이미드 필름의 제조방법 및 이에 의해 제조된 폴리이미드 필름 |
| KR102482434B1 (ko) | 2017-06-26 | 2022-12-27 | 어드밴식스 레진즈 앤드 케미컬즈 엘엘씨 | 카프로락탐-유도된 용매를 사용하는 폴리우레탄 분산액을 위한 방법 및 조성물 |
| JP6915433B2 (ja) * | 2017-08-01 | 2021-08-04 | 昭和電工マテリアルズ株式会社 | ポリアミドイミド樹脂液及びその製造方法 |
| WO2019067560A1 (en) | 2017-09-26 | 2019-04-04 | Ecolab Usa Inc. | ANTIMICROBIAL COMPOSITIONS AND ACID / ANIONIC VIROCIDES AND USES THEREOF |
| JP6927619B2 (ja) * | 2018-01-19 | 2021-09-01 | エムティーアイ カンパニー, リミテッドMti Co., Ltd. | ダイシング工程用保護コーティング剤剥離用剥離剤 |
| US12532886B2 (en) | 2018-12-04 | 2026-01-27 | Virox Technologies Inc. | Method of killing microbes using C3-C5 n-alkyl-gamma-butyrolactams and antimicrobial compositions containing same |
| AU2019391650B2 (en) * | 2018-12-04 | 2024-10-03 | Virox Technologies Inc. | C3-C5 N-alkyl-gamma-butyrolactam-containing antimicrobial compositions and uses thereof |
| US12053540B2 (en) | 2018-12-04 | 2024-08-06 | Virox Technologies Inc. | Antimicrobial compositions containing solvents including a C3-C5 N-alkyl-gamma-butyrolactam |
| US12052990B2 (en) | 2018-12-04 | 2024-08-06 | Virox Technologies Inc. | C3-C5 n-alkyl-gamma-butyrolactam containing antimicrobial compositions and methods of using same |
| KR102637130B1 (ko) * | 2019-05-22 | 2024-02-14 | 어드밴식스 레진즈 앤드 케미컬즈 엘엘씨 | 와이어 상에 에나멜 코팅을 형성하기 위한 중합체 조성물 |
| EP3756753B1 (en) | 2019-06-27 | 2022-08-31 | Sartorius Stedim Biotech GmbH | Combination of pyrrolidone based solvents for the production of porous membranes |
| KR102669766B1 (ko) * | 2019-08-27 | 2024-05-28 | 가부시끼가이샤 레조낙 | 조성물, 및 접착성 폴리머의 세정 방법 |
| AU2020408331B2 (en) | 2019-12-16 | 2023-12-14 | Ecolab Usa Inc. | Anionic surfactant impact on virucidal efficacy |
| ES2968509T3 (es) | 2020-01-15 | 2024-05-10 | Grupa Azoty S A | Composiciones disolventes líquidas que contienen triamida N-(n-butil)tiofosfórica (NBPT) y su uso como un aditivo para fertilizantes que contienen nitrógeno amida |
| KR20220142462A (ko) * | 2020-02-14 | 2022-10-21 | 엥거스 케미칼 캄파니 | 저 독성 nmp 대체물 및 이의 용도 |
| WO2021191043A1 (en) | 2020-03-25 | 2021-09-30 | Basf Se | Solution of polysulfons in n-n-butyl-2-pyrrolidone for the use of membranes |
| WO2021206683A1 (en) * | 2020-04-06 | 2021-10-14 | Basf Corporation | High-load solution concentrates of dicamba |
| KR20230065317A (ko) | 2020-09-09 | 2023-05-11 | 케이제이 케미칼즈 가부시키가이샤 | 수지 합성용 용매 및 그 용매를 사용한 합성 수지의 제조 방법 |
| US20230287180A1 (en) * | 2020-09-22 | 2023-09-14 | Elantas Europe S.R.L. | Wire enamel composition comprising polyamideimide |
| WO2022112150A1 (en) | 2020-11-30 | 2022-06-02 | Basf Se | Solution of sulfone polymers in n-tert.-butyl-2-pyrrolidone for the use of membranes |
| KR20230147687A (ko) * | 2021-03-25 | 2023-10-23 | 엘란타스 유럽 에스.알.엘. | 환경 친화적인 수계 엔지니어링 중합체 조성물 |
| WO2022214341A1 (en) | 2021-04-08 | 2022-10-13 | Basf Se | Solution of polymer p in n-tert-butyl-2-pyrrolidione for the use of membranes |
| CN118139911A (zh) * | 2021-08-26 | 2024-06-04 | 索尔维特殊聚合物美国有限责任公司 | 含有聚酰胺酰亚胺聚合物的粘度降低的组合物 |
| WO2023171679A1 (ja) | 2022-03-08 | 2023-09-14 | Ｋｊケミカルズ株式会社 | 高安全性アミド化合物を含有する組成物 |
| KR102996185B1 (ko) | 2022-07-20 | 2026-07-28 | (주)제이캠 | 비유독성 용제를 이용한 광학용 가지형 폴리우레탄 고분자의 제조 방법 |
| WO2024102348A1 (en) * | 2022-11-09 | 2024-05-16 | Illinois Tool Works Inc. | Sealant remover |
| SE546251C2 (en) * | 2022-11-29 | 2024-09-10 | Ohla Plast & Faergteknik Ab | Coating composition for components made of PVC, coated component made of PVC and method of coating a component made of PVC |
| WO2024260991A1 (en) * | 2023-06-19 | 2024-12-26 | Basf Se | Process for recovery of a polyethylene terephthalate based polymer from a polymeric material |
| CN116731551B (zh) * | 2023-06-28 | 2024-06-04 | 广东润和新材料科技有限公司 | 一种航空用途环保褪漆剂及其制备方法与应用 |
| CN118880053B (zh) * | 2024-07-22 | 2025-05-06 | 肇庆南都再生铝业有限公司 | 铝的生产工艺 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1568079C3 (de) * | 1966-02-17 | 1975-07-17 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Gewinnung von aromatischen Kohlenwasserstoffen durch selektive Extraktion von Kohlenwasserstoffgemischen |
| US3402178A (en) * | 1966-11-17 | 1968-09-17 | Allied Chem | Process for the preparation of heterocyclic iminoethers |
| FR2001768A1 (fr) | 1968-02-12 | 1969-10-03 | Gillette Co | Compositions pour l'application topique de medicaments sur la peau |
| IL35229A (en) * | 1969-10-30 | 1973-03-30 | Gaf Corp | Process for purifying gases containing sulfur dioxide |
| US3963560A (en) * | 1972-11-01 | 1976-06-15 | Gaf Corporation | Composition for deinking waste paper |
| JPS56112933A (en) * | 1980-02-12 | 1981-09-05 | Toray Ind Inc | Thermoplastic polyamide-imide copolymer and production thereof |
| JPS61276834A (ja) | 1985-06-03 | 1986-12-06 | Nippon Oil & Fats Co Ltd | ポリウレタン樹脂成形物の上塗り塗装方法 |
| US5389688A (en) * | 1989-12-11 | 1995-02-14 | Isp Investments Inc. | Water based microemulsion formulations |
| US5252535A (en) | 1992-12-23 | 1993-10-12 | Eastman Kodak Company | Thermal dye transfer receiving element with antistat backing layer |
| JPH0912910A (ja) * | 1995-04-28 | 1997-01-14 | Taoka Chem Co Ltd | テトラキスアゾ化合物及びその用途 |
| US5929274A (en) | 1995-06-07 | 1999-07-27 | Hfm International, Inc. | Method to reduce carboxybenzaldehyde isomers in terephthalic acid or isophthalic acid |
| EP0755987B1 (de) * | 1995-07-24 | 1999-06-02 | CFM GmbH Chemo-technische produkte | Farbentfernungsmittel |
| JP3644554B2 (ja) * | 1996-01-08 | 2005-04-27 | 三井・デュポンフロロケミカル株式会社 | フルオロポリマー水性エマルジョン及びその製造方法 |
| JPH10330792A (ja) * | 1997-05-28 | 1998-12-15 | T Paul Kk | 殺菌洗浄剤組成物およびその使用方法 |
| JPH1184686A (ja) * | 1997-09-01 | 1999-03-26 | Mitsubishi Gas Chem Co Inc | レジスト剥離剤組成物 |
| JP4056194B2 (ja) * | 2000-03-27 | 2008-03-05 | 独立行政法人科学技術振興機構 | カルボン酸とアミンを用いたアミド縮合物の製造方法 |
| US20030015554A1 (en) * | 2000-12-07 | 2003-01-23 | Gatzke Kenneth G. | Mehtod of cleaning an internal combustion engine using an engine cleaner composition and fluid-dispensing device for use in said method |
| DE10341811B4 (de) * | 2003-09-10 | 2006-09-28 | Ems-Chemie Ag | Katalysatorlösung zur Durchführung der anionischen Lactampolymerisation, Verfahren zu deren Herstellung und Polyamidformmasse |
| DE102004012751A1 (de) * | 2004-03-15 | 2005-10-06 | Basf Ag | Verwendung von N-Ethyl-2-pyrrolidon |
| ATE420127T1 (de) * | 2004-03-15 | 2009-01-15 | Basf Se | N-ethylpyrrolidon in der herstellung von polyurethandispersionen |
| WO2007115943A2 (de) | 2006-04-06 | 2007-10-18 | Basf Se | Verfahren zur herstellung eines n-alkyl-lactams mit verbesserter farbqualität |
| EP2005824A1 (de) * | 2007-06-21 | 2008-12-24 | Bayer CropScience AG | Wirkstoffsuspensionen in Glycerin |
| JP5301872B2 (ja) * | 2007-08-29 | 2013-09-25 | 国立大学法人東北大学 | チオール基含有感紫外線化合物および、その用途 |
| JP4702351B2 (ja) * | 2007-11-14 | 2011-06-15 | セイコーエプソン株式会社 | ２次電池電極用インク、リチウムイオン電池、電子機器及び車両 |
| WO2010142617A1 (de) | 2009-06-10 | 2010-12-16 | Basf Se | Neue lösungsmittel in der herstellung von polyurethandispersionen |
| BE1020269A5 (nl) * | 2012-01-17 | 2013-07-02 | Taminco | Gebruik van vervangende oplosmiddelen voor n-methylpyrrolidon (nmp). |
-
2012
- 2012-01-17 BE BE2012/0037A patent/BE1020269A5/nl active
-
2013
- 2013-01-17 EP EP13703739.6A patent/EP2804940B1/en not_active Revoked
- 2013-01-17 KR KR1020147022834A patent/KR101515848B1/ko active Active
- 2013-01-17 MX MX2014008606A patent/MX363336B/es unknown
- 2013-01-17 CA CA2861145A patent/CA2861145C/en active Active
- 2013-01-17 US US14/372,411 patent/US20150057375A1/en not_active Abandoned
- 2013-01-17 WO PCT/EP2013/050852 patent/WO2013107822A1/en not_active Ceased
- 2013-01-17 JP JP2014551652A patent/JP2015511935A/ja not_active Withdrawn
- 2013-01-17 PL PL13703739T patent/PL2804940T3/pl unknown
- 2013-01-17 IN IN6843DEN2014 patent/IN2014DN06843A/en unknown
- 2013-01-17 DK DK13703739.6T patent/DK2804940T3/en active
- 2013-01-17 CN CN201380010688.5A patent/CN104136595A/zh active Pending
- 2013-01-17 ES ES13703739.6T patent/ES2691268T3/es active Active
-
2017
- 2017-02-17 JP JP2017027841A patent/JP2017095520A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| MX363336B (es) | 2019-03-19 |
| EP2804940B1 (en) | 2018-09-19 |
| CN104136595A (zh) | 2014-11-05 |
| EP2804940A1 (en) | 2014-11-26 |
| BE1020269A5 (nl) | 2013-07-02 |
| ES2691268T3 (es) | 2018-11-26 |
| WO2013107822A1 (en) | 2013-07-25 |
| PL2804940T3 (pl) | 2019-02-28 |
| KR20140111038A (ko) | 2014-09-17 |
| CA2861145C (en) | 2020-03-24 |
| MX2014008606A (es) | 2014-08-27 |
| KR101515848B1 (ko) | 2015-04-29 |
| JP2015511935A (ja) | 2015-04-23 |
| US20150057375A1 (en) | 2015-02-26 |
| IN2014DN06843A (enExample) | 2015-05-22 |
| JP2017095520A (ja) | 2017-06-01 |
| CA2861145A1 (en) | 2013-07-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2804940B1 (en) | Use of improved n-alkyl pyrrolidone solvents | |
| US9351484B2 (en) | N-alkyl lactam ethers, and compositions and uses thereof | |
| CA2851390C (fr) | Composition, procede d'obtention de la composition et formulation phytosanitaire la comprenant | |
| TW200936045A (en) | Use of esteramides, novel esteramides and process for preparing esteramides | |
| CN104782624A (zh) | 生产乳酰胺化合物的方法、新的乳酰胺化合物和含有乳酰胺化合物的制剂 | |
| CN105143195A (zh) | 作为载体的糠醛衍生物 | |
| WO2005090447A2 (de) | Verwendung von n-ethyl-2-pyrrolidon | |
| HUE028200T2 (en) | Improvements to Organic Compounds | |
| JP2011518867A (ja) | エーテルアミド型化合物、その製造方法及び使用 | |
| FR3040995A1 (fr) | Utilisation de composes comprenant une fonction sulfoxyde ou sulfone et une fonction amide comme solvants et nouveaux solvants | |
| CN103328444A (zh) | N-取代的2-吡咯烷酮-4-甲酸酯作为溶剂的用途 | |
| CN103052622B (zh) | 配制品 | |
| CN109851760A (zh) | 阳离子改性环氧树脂、改性环氧树脂聚合物、乳液及其制备方法和涂料及应用 | |
| JPH0585908A (ja) | 除草剤プロパニルの安定な溶液型組成物及び乳剤型組成物 | |
| WO2005092953A1 (de) | Verwendung von n-methylcaprolactam | |
| EP1059292B1 (en) | New adamantane derivative and aqueous disinfectant composition containing it | |
| CA3014540C (en) | High purity disorbate ester of triethylene glycol | |
| CN103025704B (zh) | 配制品 | |
| CN109423102A (zh) | 一种新型防沉剂 | |
| WO2017139966A1 (en) | Preparation of high purity disorbate ester of triethylene glycol |