PL150297B1 - - Google Patents

Info

Publication number

PL150297B1

PL150297B1 PL274176A PL27417686A PL150297B1 PL 150297 B1 PL150297 B1 PL 150297B1 PL 274176 A PL274176 A PL 274176A PL 27417686 A PL27417686 A PL 27417686A PL 150297 B1 PL150297 B1 PL 150297B1

Authority

PL

Poland

Prior art keywords

emulsifier

formula

measure according

acid

derived

Prior art date

1986-12-05

Links

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• -1 diethylethanolamine ester Chemical class 0.000 claims description 139
• 150000001412 amines Chemical class 0.000 claims description 99
• 239000011780 sodium chloride Substances 0.000 claims description 91
• 125000004432 carbon atoms Chemical group C* 0.000 claims description 84
• 150000003839 salts Chemical class 0.000 claims description 83
• 239000003995 emulsifying agent Substances 0.000 claims description 71
• 239000000203 mixture Substances 0.000 claims description 63
• 239000002253 acid Substances 0.000 claims description 61
• 238000000034 method Methods 0.000 claims description 59
• 229920000768 polyamine Polymers 0.000 claims description 58
• 125000001183 hydrocarbyl group Chemical group 0.000 claims description 52
• 150000002148 esters Chemical class 0.000 claims description 41
• 150000001408 amides Chemical class 0.000 claims description 39
• 150000008064 anhydrides Chemical class 0.000 claims description 37
• 125000003118 aryl group Chemical group 0.000 claims description 35
• 125000002947 alkylene group Chemical group 0.000 claims description 34
• 239000000839 emulsion Substances 0.000 claims description 34
• 125000001931 aliphatic group Chemical group 0.000 claims description 30
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 26
• 150000001875 compounds Chemical class 0.000 claims description 24
• RINCXYDBBGOEEQ-UHFFFAOYSA-N Succinic anhydride Chemical compound O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 claims description 23
• 125000001424 substituent group Chemical group 0.000 claims description 23
• 239000003795 chemical substances by application Substances 0.000 claims description 22
• 125000002924 primary amino group Chemical class [H]N([H])* 0.000 claims description 21
• 239000012071 phase Substances 0.000 claims description 18
• 229940014800 succinic anhydride Drugs 0.000 claims description 18
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
• 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 15
• AVXURJPOCDRRFD-UHFFFAOYSA-N hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 15
• BFSVOASYOCHEOV-UHFFFAOYSA-N Diethylethanolamine Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims description 14
• 125000003277 amino group Chemical group 0.000 claims description 14
• QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 14
• 239000004215 Carbon black (E152) Substances 0.000 claims description 12
• 150000003512 tertiary amines Chemical class 0.000 claims description 12
• 125000003342 alkenyl group Chemical group 0.000 claims description 10
• 239000008346 aqueous phase Substances 0.000 claims description 9
• 150000002430 hydrocarbons Chemical class 0.000 claims description 9
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
• VQTUBCCKSQIDNK-UHFFFAOYSA-N isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 7
• 150000004982 aromatic amines Chemical class 0.000 claims description 6
• 230000001590 oxidative Effects 0.000 claims description 6
• 125000005702 oxyalkylene group Chemical class 0.000 claims description 6
• 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 claims description 6
• 229920002367 Polyisobutene Polymers 0.000 claims description 5
• 125000005466 alkylenyl group Chemical group 0.000 claims description 5
• 125000000962 organic group Chemical group 0.000 claims description 5
• 239000007762 w/o emulsion Substances 0.000 claims description 3
• 229940004296 Formula 21 Drugs 0.000 claims description 2
• OCJYIGYOJCODJL-UHFFFAOYSA-N Meclizine Chemical group CC1=CC=CC(CN2CCN(CC2)C(C=2C=CC=CC=2)C=2C=CC(Cl)=CC=2)=C1 OCJYIGYOJCODJL-UHFFFAOYSA-N 0.000 claims description 2
• 239000003921 oil Substances 0.000 description 64
• 235000019198 oils Nutrition 0.000 description 60
• 150000001298 alcohols Chemical class 0.000 description 48
• 239000000047 product Substances 0.000 description 36
• 150000001732 carboxylic acid derivatives Chemical class 0.000 description 27
• 229910052757 nitrogen Inorganic materials 0.000 description 25
• LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 23
• 238000002360 preparation method Methods 0.000 description 22
• 150000001336 alkenes Chemical class 0.000 description 21
• 125000000217 alkyl group Chemical group 0.000 description 21
• 229910052801 chlorine Inorganic materials 0.000 description 21
• 239000007788 liquid Substances 0.000 description 21
• 239000000460 chlorine Substances 0.000 description 20
• ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 19
• 229920000642 polymer Polymers 0.000 description 19
• 229920000098 polyolefin Polymers 0.000 description 18
• 150000007513 acids Chemical class 0.000 description 16
• QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
• 239000012445 acidic reagent Substances 0.000 description 15
• 239000000654 additive Substances 0.000 description 15
• 230000015572 biosynthetic process Effects 0.000 description 15
• 150000001735 carboxylic acids Chemical class 0.000 description 15
• 238000006243 chemical reaction Methods 0.000 description 14
• RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Natural products OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 12
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
• QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 11
• 238000009833 condensation Methods 0.000 description 10
• 230000005494 condensation Effects 0.000 description 10
• 230000000875 corresponding Effects 0.000 description 10
• 238000005755 formation reaction Methods 0.000 description 10
• 125000000623 heterocyclic group Chemical group 0.000 description 10
• 125000003545 alkoxy group Chemical group 0.000 description 9
• 239000003153 chemical reaction reagent Substances 0.000 description 9
• OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 9
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 9
• 239000003381 stabilizer Substances 0.000 description 9
• IMNIMPAHZVJRPE-UHFFFAOYSA-N DABCO Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 8
• VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
• OYHQOLUKZRVURQ-IXWMQOLASA-N Linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 8
• ZQPPMHVWECSIRJ-KTKRTIGZSA-N Oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 8
• 230000000996 additive Effects 0.000 description 8
• 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 8
• 239000007795 chemical reaction product Substances 0.000 description 8
• 238000005660 chlorination reaction Methods 0.000 description 8
• 150000002829 nitrogen Chemical group 0.000 description 8
• GLUUGHFHXGJENI-UHFFFAOYSA-N piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 8
• 150000003335 secondary amines Chemical class 0.000 description 8
• 239000005977 Ethylene Substances 0.000 description 7
• KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 7
• 229910052799 carbon Inorganic materials 0.000 description 7
• HZAXFHJVJLSVMW-UHFFFAOYSA-N ethanolamine Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 7
• 239000000194 fatty acid Substances 0.000 description 7
• PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 7
• 239000004615 ingredient Substances 0.000 description 7
• PAFZNILMFXTMIY-UHFFFAOYSA-N Cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 6
• 229920001451 Polypropylene glycol Polymers 0.000 description 6
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
• 235000014113 dietary fatty acids Nutrition 0.000 description 6
• VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
• BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
• IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
• 229920001281 polyalkylene Polymers 0.000 description 6
• 229920000647 polyepoxide Polymers 0.000 description 6
• XBDQKXXYIPTUBI-UHFFFAOYSA-N propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
• 239000002904 solvent Substances 0.000 description 6
• WXZMFSXDPGVJKK-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 5
• MTHSVFCYNBDYFN-UHFFFAOYSA-N Diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
• POULHZVOKOAJMA-UHFFFAOYSA-N Lauric acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 5
• 235000021355 Stearic acid Nutrition 0.000 description 5
• IIACRCGMVDHOTQ-UHFFFAOYSA-N Sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 5
• 235000011054 acetic acid Nutrition 0.000 description 5
• 238000007792 addition Methods 0.000 description 5
• OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
• 229920001577 copolymer Polymers 0.000 description 5
• 239000003085 diluting agent Substances 0.000 description 5
• 150000004665 fatty acids Chemical class 0.000 description 5
• 239000012530 fluid Substances 0.000 description 5
• 235000011187 glycerol Nutrition 0.000 description 5
• 150000002334 glycols Chemical class 0.000 description 5
• 238000002156 mixing Methods 0.000 description 5
• YNAVUWVOSKDBBP-UHFFFAOYSA-N morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 5
• 229940113083 morpholine Drugs 0.000 description 5
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
• 125000004433 nitrogen atoms Chemical group N* 0.000 description 5
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 5
• 150000002989 phenols Chemical class 0.000 description 5
• 229920001223 polyethylene glycol Polymers 0.000 description 5
• 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
• 239000008117 stearic acid Substances 0.000 description 5
• 239000000126 substance Substances 0.000 description 5
• 235000011044 succinic acid Nutrition 0.000 description 5
• VZCYOOQTPOCHFL-OWOJBTEDSA-N (E)-but-2-enedioate;hydron Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
• PIICEJLVQHRZGT-UHFFFAOYSA-N 1,2-ethanediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 4
• UKMSUNONTOPOIO-UHFFFAOYSA-N Behenic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 4
• UNXHWFMMPAWVPI-QWWZWVQMSA-N D-Threitol Natural products OC[C@@H](O)[C@H](O)CO UNXHWFMMPAWVPI-QWWZWVQMSA-N 0.000 description 4
• 239000004386 Erythritol Substances 0.000 description 4
• UNXHWFMMPAWVPI-ZXZARUISSA-N Erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 4
• 229940009714 Erythritol Drugs 0.000 description 4
• 229940012017 Ethylenediamine Drugs 0.000 description 4
• TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 4
• 239000005642 Oleic acid Substances 0.000 description 4
• IPCSVZSSVZVIGE-UHFFFAOYSA-N Palmitic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
• 229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
• CXMXRPHRNRROMY-UHFFFAOYSA-N Sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
• 238000010306 acid treatment Methods 0.000 description 4
• 125000002877 alkyl aryl group Chemical group 0.000 description 4
• 125000003710 aryl alkyl group Chemical group 0.000 description 4
• 239000012141 concentrate Substances 0.000 description 4
• 230000001804 emulsifying Effects 0.000 description 4
• 235000019414 erythritol Nutrition 0.000 description 4
• 229940031098 ethanolamine Drugs 0.000 description 4
• 150000002170 ethers Chemical class 0.000 description 4
• 125000002768 hydroxyalkyl group Chemical group 0.000 description 4
• RRHGJUQNOFWUDK-UHFFFAOYSA-N isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
• 235000020778 linoleic acid Nutrition 0.000 description 4
• 239000000376 reactant Substances 0.000 description 4
• 239000011541 reaction mixture Substances 0.000 description 4
• LSNNMFCWUKXFEE-UHFFFAOYSA-N sulfonic acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 4
• 239000004094 surface-active agent Substances 0.000 description 4
• YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
• 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 3
• PLIKAWJENQZMHA-UHFFFAOYSA-N 4-Aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 3
• LHIJANUOQQMGNT-UHFFFAOYSA-N Aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 3
• WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
• 229920001748 Polybutylene Polymers 0.000 description 3
• 239000002202 Polyethylene glycol Substances 0.000 description 3
• PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
• CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
• 125000003158 alcohol group Chemical group 0.000 description 3
• 125000002723 alicyclic group Chemical group 0.000 description 3
• 229910052783 alkali metal Inorganic materials 0.000 description 3
• 238000005804 alkylation reaction Methods 0.000 description 3
• 125000006294 amino alkylene group Chemical group 0.000 description 3
• 239000003945 anionic surfactant Substances 0.000 description 3
• 125000004429 atoms Chemical group 0.000 description 3
• KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
• 239000003093 cationic surfactant Substances 0.000 description 3
• 125000001309 chloro group Chemical group Cl* 0.000 description 3
• 239000007859 condensation product Substances 0.000 description 3
• 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 3
• 150000004985 diamines Chemical class 0.000 description 3
• 125000003700 epoxy group Chemical group 0.000 description 3
• QUSNBJAOOMFDIB-UHFFFAOYSA-N ethyl amine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 3
• 235000019253 formic acid Nutrition 0.000 description 3
• 125000005842 heteroatoms Chemical group 0.000 description 3
• 150000002429 hydrazines Chemical class 0.000 description 3
• 239000001257 hydrogen Substances 0.000 description 3
• 229910052739 hydrogen Inorganic materials 0.000 description 3
• 239000000314 lubricant Substances 0.000 description 3
• 150000002780 morpholines Chemical class 0.000 description 3
• 239000002736 nonionic surfactant Substances 0.000 description 3
• 235000021313 oleic acid Nutrition 0.000 description 3
• 230000020477 pH reduction Effects 0.000 description 3
• 150000004885 piperazines Chemical class 0.000 description 3
• 150000003053 piperidines Chemical class 0.000 description 3
• GOOHAUXETOMSMM-UHFFFAOYSA-N propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
• BPQQTUXANYXVAA-UHFFFAOYSA-N silicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 3
• 238000003756 stirring Methods 0.000 description 3
• 150000003444 succinic acids Chemical class 0.000 description 3
• 150000003460 sulfonic acids Chemical class 0.000 description 3
• 125000004434 sulfur atoms Chemical group 0.000 description 3
• 239000010689 synthetic lubricating oil Substances 0.000 description 3
• WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 2
• WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-Butanediol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
• VXNZUUAINFGPBY-UHFFFAOYSA-N 1-butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
• RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 2
• MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (Z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 description 2
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
• WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 description 2
• WUGQZFFCHPXWKQ-UHFFFAOYSA-N 3-aminopropanol Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 2
• VACHUYIREGFMSP-SJORKVTESA-N 9,10-Dihydroxystearic acid Natural products CCCCCCCC[C@@H](O)[C@@H](O)CCCCCCCC(O)=O VACHUYIREGFMSP-SJORKVTESA-N 0.000 description 2
• WNLRTRBMVRJNCN-UHFFFAOYSA-N Adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
• XXROGKLTLUQVRX-UHFFFAOYSA-N Allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
• VSCWAEJMTAWNJL-UHFFFAOYSA-K Aluminium chloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
• IMUDHTPIFIBORV-UHFFFAOYSA-N Aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 description 2
• 235000021357 Behenic acid Nutrition 0.000 description 2
• FERIUCNNQQJTOY-UHFFFAOYSA-N Butanoic acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
• FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
• WQZGKKKJIJFFOK-GASJEMHNSA-N D-Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
• FBPFZTCFMRRESA-KAZBKCHUSA-N D-Mannitol Natural products OC[C@@H](O)[C@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KAZBKCHUSA-N 0.000 description 2
• FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
• RPNUMPOLZDHAAY-UHFFFAOYSA-N DETA Chemical class NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
• OEKPKBBXXDGXNB-IBISWUOJSA-N Digitalose Natural products CO[C@H]1[C@@H](O)[C@@H](C)O[C@@H](O)[C@@H]1O OEKPKBBXXDGXNB-IBISWUOJSA-N 0.000 description 2
• VJHINFRRDQUWOJ-UHFFFAOYSA-N Dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 2
• USIUVYZYUHIAEV-UHFFFAOYSA-N Diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
• RRAFCDWBNXTKKO-UHFFFAOYSA-N Eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
• BJHIKXHVCXFQLS-UYFOZJQFSA-N Fructose Natural products OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 description 2
• RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
• MNQZXJOMYWMBOU-UHFFFAOYSA-N Glyceraldehyde Chemical compound OCC(O)C=O MNQZXJOMYWMBOU-UHFFFAOYSA-N 0.000 description 2
• KRHYYFGTRYWZRS-UHFFFAOYSA-N HF Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
• FUZZWVXGSFPDMH-UHFFFAOYSA-N Hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
• 239000005639 Lauric acid Substances 0.000 description 2
• FPYJFEHAWHCUMM-UHFFFAOYSA-N Maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
• FBPFZTCFMRRESA-KVTDHHQDSA-N Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
• 235000021360 Myristic acid Nutrition 0.000 description 2
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