OA16693A - - Google Patents

Info

Publication number

OA16693A

OA16693A OA1201400567 OA16693A OA 16693 A OA16693 A OA 16693A OA 1201400567 OA1201400567 OA 1201400567 OA 16693 A OA16693 A OA 16693A

Authority

OA

OAPI

Prior art keywords

cellulose

ether

methyl

acid

hydroxyl groups

Prior art date

2012-06-25

Links

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• 229920002678 cellulose Polymers 0.000 claims description 101
• 239000001913 cellulose Substances 0.000 claims description 98
• 239000000463 material Substances 0.000 claims description 86
• 239000000203 mixture Substances 0.000 claims description 77
• 239000002253 acid Substances 0.000 claims description 50
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 50
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 35
• RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 26
• 239000002904 solvent Substances 0.000 claims description 23
• CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 22
• -1 benzindazones Chemical class 0.000 claims description 22
• 235000013305 food Nutrition 0.000 claims description 20
• 230000035699 permeability Effects 0.000 claims description 20
• 229910052760 oxygen Inorganic materials 0.000 claims description 18
• YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 16
• 229920000742 Cotton Polymers 0.000 claims description 14
• 239000007788 liquid Substances 0.000 claims description 14
• 239000001301 oxygen Substances 0.000 claims description 14
• MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 14
• 125000004432 carbon atoms Chemical group C* 0.000 claims description 13
• XEKOWRVHYACXOJ-UHFFFAOYSA-N acetic acid ethyl ester Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
• 239000003795 chemical substances by application Substances 0.000 claims description 12
• 150000002148 esters Chemical class 0.000 claims description 10
• 150000008064 anhydrides Chemical class 0.000 claims description 9
• 239000000835 fiber Substances 0.000 claims description 9
• 238000000034 method Methods 0.000 claims description 9
• ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 8
• RDOXTESZEPMUJZ-UHFFFAOYSA-N Anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims description 8
• VZGDMQKNWNREIO-UHFFFAOYSA-N Carbon tetrachloride Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 8
• MVPPADPHJFYWMZ-UHFFFAOYSA-N Chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 8
• SBZXBUIDTXKZTM-UHFFFAOYSA-N Diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 claims description 8
• KXKVLQRXCPHEJC-UHFFFAOYSA-N Methyl acetate Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 8
• UAEPNZWRGJTJPN-UHFFFAOYSA-N Methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 claims description 8
• YFNKIDBQEZZDLK-UHFFFAOYSA-N Triethylene glycol dimethyl ether Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 claims description 8
• UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 8
• HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 8
• MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 claims description 8
• XTHFKEDIFFGKHM-UHFFFAOYSA-N dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims description 8
• 238000001035 drying Methods 0.000 claims description 8
• 239000004744 fabric Substances 0.000 claims description 8
• 238000010438 heat treatment Methods 0.000 claims description 8
• VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 8
• UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims description 8
• YMWUJEATGCHHMB-UHFFFAOYSA-N methylene dichloride Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 8
• 239000003208 petroleum Substances 0.000 claims description 8
• WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 8
• DPBLXKKOBLCELK-UHFFFAOYSA-N Pentylamine Chemical class CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 claims description 7
• 150000001805 chlorine compounds Chemical class 0.000 claims description 7
• 230000000269 nucleophilic Effects 0.000 claims description 7
• CTQNGGLPUBDAKN-UHFFFAOYSA-N o-xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 7
• ZMANZCXQSJIPKH-UHFFFAOYSA-N triethylamine Chemical class CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 7
• 239000008096 xylene Substances 0.000 claims description 7
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 6
• 238000004381 surface treatment Methods 0.000 claims description 6
• 229920001046 Nanocellulose Polymers 0.000 claims description 5
• 235000013334 alcoholic beverage Nutrition 0.000 claims description 5
• 150000001649 bromium compounds Chemical class 0.000 claims description 5
• 235000020965 cold beverage Nutrition 0.000 claims description 5
• 235000012171 hot beverage Nutrition 0.000 claims description 5
• 150000004694 iodide salts Chemical class 0.000 claims description 5
• 150000002561 ketenes Chemical class 0.000 claims description 5
• 235000019520 non-alcoholic beverage Nutrition 0.000 claims description 5
• MZLKHPDPHGHSOY-UHFFFAOYSA-N (2,3-dioxoindole-1-carbonyl) 2,3-dioxoindole-1-carboxylate Chemical compound O=C1C(=O)C2=CC=CC=C2N1C(=O)OC(=O)N1C2=CC=CC=C2C(=O)C1=O MZLKHPDPHGHSOY-UHFFFAOYSA-N 0.000 claims description 4
• OVRRJBSHBOXFQE-UHFFFAOYSA-N 1,1,2,2-tetrabromoethene Chemical group BrC(Br)=C(Br)Br OVRRJBSHBOXFQE-UHFFFAOYSA-N 0.000 claims description 4
• WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 4
• KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 claims description 4
• ARAFEULRMHFMDE-UHFFFAOYSA-N 1,3-oxazolidine-2,5-dione Chemical class O=C1CNC(=O)O1 ARAFEULRMHFMDE-UHFFFAOYSA-N 0.000 claims description 4
• RKIPCZGWRCITOW-UHFFFAOYSA-N 1-cycloundecyl-1,5-diazacycloundecane Chemical class C1CCCCCCCCCC1N1CCCNCCCCCC1 RKIPCZGWRCITOW-UHFFFAOYSA-N 0.000 claims description 4
• KJUGUADJHNHALS-UHFFFAOYSA-N 1H-tetrazole Substances C=1N=NNN=1 KJUGUADJHNHALS-UHFFFAOYSA-N 0.000 claims description 4
• PTTPXKJBFFKCEK-UHFFFAOYSA-N 2,6-dimethylheptan-4-one Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 claims description 4
• SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-Methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 claims description 4
• OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 claims description 4
• POAOYUHQDCAZBD-UHFFFAOYSA-N 2-Butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 4
• XNLICIUVMPYHGG-UHFFFAOYSA-N 2-Pentanone Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 claims description 4
• UJOBWOGCFQCDNV-UHFFFAOYSA-N Carbazole Natural products C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 4
• YGGRMHGSIHLAMS-UHFFFAOYSA-N ClNS=O Chemical class ClNS=O YGGRMHGSIHLAMS-UHFFFAOYSA-N 0.000 claims description 4
• IMNIMPAHZVJRPE-UHFFFAOYSA-N DABCO Chemical class C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims description 4
• RRQYJINTUHWNHW-UHFFFAOYSA-N Diethylene glycol diethyl ether Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 claims description 4
• USIUVYZYUHIAEV-UHFFFAOYSA-N Diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 4
• SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 4
• BZLVMXJERCGZMT-UHFFFAOYSA-N MeOtBu Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 4
• TZIHFWKZFHZASV-UHFFFAOYSA-N Methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 claims description 4
• NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims description 4
• XJRBAMWJDBPFIM-UHFFFAOYSA-N Methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims description 4
• 210000001724 Microfibrils Anatomy 0.000 claims description 4
• TVMXDCGIABBOFY-UHFFFAOYSA-N Octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 4
• 239000005662 Paraffin oil Substances 0.000 claims description 4
• YKYONYBAUNKHLG-UHFFFAOYSA-N Propyl acetate Chemical compound CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 claims description 4
• 240000000111 Saccharum officinarum Species 0.000 claims description 4
• 235000007201 Saccharum officinarum Nutrition 0.000 claims description 4
• YBBRCQOCSYXUOC-UHFFFAOYSA-N Sulfuryl chloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims description 4
• 210000003135 Vibrissae Anatomy 0.000 claims description 4
• 229940111121 antirheumatic drugs Quinolines Drugs 0.000 claims description 4
• 150000001539 azetidines Chemical class 0.000 claims description 4
• 150000001541 aziridines Chemical class 0.000 claims description 4
• 150000001556 benzimidazoles Chemical class 0.000 claims description 4
• FUZZWVXGSFPDMH-UHFFFAOYSA-M caproate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 claims description 4
• NBYQXBYMEUOBON-UHFFFAOYSA-N carbamothioyl chloride Chemical class NC(Cl)=S NBYQXBYMEUOBON-UHFFFAOYSA-N 0.000 claims description 4
• CKDWPUIZGOQOOM-UHFFFAOYSA-N carbamoyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 claims description 4
• 150000001716 carbazoles Chemical class 0.000 claims description 4
• 150000004650 carbonic acid diesters Chemical class 0.000 claims description 4
• XDTMQSROBMDMFD-UHFFFAOYSA-N cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 4
• RGSFGYAAUTVSQA-UHFFFAOYSA-N cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 4
• 229940019778 diethylene glycol diethyl ether Drugs 0.000 claims description 4
• 229940028356 diethylene glycol monobutyl ether Drugs 0.000 claims description 4
• 125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 claims description 4
• LCGLNKUTAGEVQW-UHFFFAOYSA-N dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 4
• YNQLUTRBYVCPMQ-UHFFFAOYSA-N ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 4
• 239000008079 hexane Substances 0.000 claims description 4
• WZELXJBMMZFDDU-UHFFFAOYSA-N imidazol-2-one Chemical class O=C1N=CC=N1 WZELXJBMMZFDDU-UHFFFAOYSA-N 0.000 claims description 4
• 150000002460 imidazoles Chemical class 0.000 claims description 4
• 150000002462 imidazolines Chemical class 0.000 claims description 4
• QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical class C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 claims description 4
• 150000002475 indoles Chemical class 0.000 claims description 4
• 150000002476 indolines Chemical class 0.000 claims description 4
• 150000002513 isocyanates Chemical class 0.000 claims description 4
• 150000002537 isoquinolines Chemical class 0.000 claims description 4
• 150000002545 isoxazoles Chemical class 0.000 claims description 4
• 239000003350 kerosene Substances 0.000 claims description 4
• AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 claims description 4
• 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
• 150000002780 morpholines Chemical class 0.000 claims description 4
• IMNFDUFMRHMDMM-UHFFFAOYSA-N n-heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 4
• 150000005054 naphthyridines Chemical class 0.000 claims description 4
• 150000004866 oxadiazoles Chemical class 0.000 claims description 4
• 150000002916 oxazoles Chemical class 0.000 claims description 4
• 150000002918 oxazolines Chemical class 0.000 claims description 4
• OFBQJSOFQDEBGM-UHFFFAOYSA-N pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 4
• 150000004885 piperazines Chemical class 0.000 claims description 4
• 150000003217 pyrazoles Chemical class 0.000 claims description 4
• 150000003222 pyridines Chemical class 0.000 claims description 4
• 150000003230 pyrimidines Chemical class 0.000 claims description 4
• 150000003233 pyrroles Chemical class 0.000 claims description 4
• 150000003235 pyrrolidines Chemical class 0.000 claims description 4
• 150000004040 pyrrolidinones Chemical class 0.000 claims description 4
• 150000003248 quinolines Chemical class 0.000 claims description 4
• LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 4
• 150000003536 tetrazoles Chemical class 0.000 claims description 4
• 150000004867 thiadiazoles Chemical class 0.000 claims description 4
• 150000003567 thiocyanates Chemical class 0.000 claims description 4
• 150000003852 triazoles Chemical class 0.000 claims description 4
• JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 claims description 4
• 150000003219 pyrazolines Chemical class 0.000 claims description 3
• 150000003918 triazines Chemical class 0.000 claims description 3
• 150000007530 organic bases Chemical class 0.000 claims description 2
• 150000003053 piperidines Chemical class 0.000 claims description 2
• 235000010980 cellulose Nutrition 0.000 description 73
• 238000000576 coating method Methods 0.000 description 34
• 239000011248 coating agent Substances 0.000 description 31
• 206010053317 Hydrophobia Diseases 0.000 description 8
• 238000006243 chemical reaction Methods 0.000 description 8
• JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
• 230000004888 barrier function Effects 0.000 description 6
• 125000005647 linker group Chemical group 0.000 description 6
• 238000006467 substitution reaction Methods 0.000 description 6
• 239000007789 gas Substances 0.000 description 5
• 150000004820 halides Chemical class 0.000 description 5
• 238000004806 packaging method and process Methods 0.000 description 5
• 239000000047 product Substances 0.000 description 5
• 239000007787 solid Substances 0.000 description 5
• 239000000126 substance Substances 0.000 description 5
• 239000000758 substrate Substances 0.000 description 5
• 238000010521 absorption reaction Methods 0.000 description 4
• 230000005540 biological transmission Effects 0.000 description 4
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 4
• 238000004132 cross linking Methods 0.000 description 4
• 150000001991 dicarboxylic acids Chemical class 0.000 description 4
• 125000001424 substituent group Chemical group 0.000 description 4
• QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
• 150000008065 acid anhydrides Chemical class 0.000 description 3
• 230000001580 bacterial Effects 0.000 description 3
• 239000003153 chemical reaction reagent Substances 0.000 description 3
• 150000001875 compounds Chemical class 0.000 description 3
• BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 3
• 238000005259 measurement Methods 0.000 description 3
• 230000004048 modification Effects 0.000 description 3
• 238000006011 modification reaction Methods 0.000 description 3
• 239000004033 plastic Substances 0.000 description 3
• 229920003023 plastic Polymers 0.000 description 3
• 229920000642 polymer Polymers 0.000 description 3
• XBDQKXXYIPTUBI-UHFFFAOYSA-N propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
• 239000004094 surface-active agent Substances 0.000 description 3
• FERIUCNNQQJTOY-UHFFFAOYSA-N Butanoic acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
• 229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
• 229920003043 Cellulose fiber Polymers 0.000 description 2
• WHTNHYRHHHFFBV-UHFFFAOYSA-N ClNS(=O)=O Chemical class ClNS(=O)=O WHTNHYRHHHFFBV-UHFFFAOYSA-N 0.000 description 2
• 241000196324 Embryophyta Species 0.000 description 2
• 102000004190 Enzymes Human genes 0.000 description 2
• 108090000790 Enzymes Proteins 0.000 description 2
• 239000002841 Lewis acid Substances 0.000 description 2
• 239000000020 Nitrocellulose Substances 0.000 description 2
• 229920000297 Rayon Polymers 0.000 description 2
• 239000002250 absorbent Substances 0.000 description 2
• 230000002745 absorbent Effects 0.000 description 2
• 125000000217 alkyl group Chemical group 0.000 description 2
• 239000001768 carboxy methyl cellulose Substances 0.000 description 2
• 235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
• 239000008112 carboxymethyl-cellulose Substances 0.000 description 2
• 239000003054 catalyst Substances 0.000 description 2
• 238000001212 derivatisation Methods 0.000 description 2
• NQGIJDNPUZEBRU-UHFFFAOYSA-N dodecanoyl chloride Chemical compound CCCCCCCCCCCC(Cl)=O NQGIJDNPUZEBRU-UHFFFAOYSA-N 0.000 description 2
• 238000005516 engineering process Methods 0.000 description 2
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
• 230000005660 hydrophilic surface Effects 0.000 description 2
• 150000002576 ketones Chemical class 0.000 description 2
• 150000007517 lewis acids Chemical class 0.000 description 2
• 125000002950 monocyclic group Chemical group 0.000 description 2
• 125000001419 myristoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
• 229920001220 nitrocellulos Polymers 0.000 description 2
• 230000003000 nontoxic Effects 0.000 description 2
• 231100000252 nontoxic Toxicity 0.000 description 2
• 125000003367 polycyclic group Chemical group 0.000 description 2
• 239000000376 reactant Substances 0.000 description 2
• 239000005871 repellent Substances 0.000 description 2
• 229920005989 resin Polymers 0.000 description 2
• 239000011347 resin Substances 0.000 description 2
• LPWCRLGKYWVLHQ-UHFFFAOYSA-N tetradecanoyl chloride Chemical compound CCCCCCCCCCCCCC(Cl)=O LPWCRLGKYWVLHQ-UHFFFAOYSA-N 0.000 description 2
• LNAZSHAWQACDHT-XIYTZBAFSA-N (2R,3R,4S,5R,6S)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2R,3R,4S,5R,6R)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
• HKQOBOMRSSHSTC-DIBAFDJWSA-N (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol;[(2R,3R,4S,5R,6S)-4,5,6-triacetyloxy-3-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl acetate;[( Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O)[C@H](O)[C@H]1O.CC(=O)OC[C@H]1O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1O[C@H]1[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1.CCC(=O)OC[C@H]1O[C@@H](OC(=O)CC)[C@H](OC(=O)CC)[C@@H](OC(=O)CC)[C@@H]1O[C@H]1[C@H](OC(=O)CC)[C@@H](OC(=O)CC)[C@H](OC(=O)CC)[C@@H](COC(=O)CC)O1 HKQOBOMRSSHSTC-DIBAFDJWSA-N 0.000 description 1
• VUKAUDKDFVSVFT-UHFFFAOYSA-N 2-[6-[4,5-bis(2-hydroxypropoxy)-2-(2-hydroxypropoxymethyl)-6-methoxyoxan-3-yl]oxy-4,5-dimethoxy-2-(methoxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)-5-methoxyoxane-3,4-diol Chemical compound COC1C(OC)C(OC2C(C(O)C(OC)C(CO)O2)O)C(COC)OC1OC1C(COCC(C)O)OC(OC)C(OCC(C)O)C1OCC(C)O VUKAUDKDFVSVFT-UHFFFAOYSA-N 0.000 description 1
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