JP2551959C - - Google Patents

Info

Publication number

JP2551959C

JP2551959C JP2551959C JP 2551959 C JP2551959 C JP 2551959C JP 2551959 C JP2551959 C JP 2551959C

Authority

JP

Japan

Prior art keywords

substituted

hydrocarbon

composition

amine

group

Prior art date

1999-02-10

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired - Lifetime

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• -1 cycloaliphatic Chemical group 0.000 claims description 125
• 239000000203 mixture Substances 0.000 claims description 125
• 150000001412 amines Chemical class 0.000 claims description 94
• 125000004432 carbon atom Chemical group C* 0.000 claims description 86
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 67
• 150000008064 anhydrides Chemical class 0.000 claims description 65
• 239000002253 acid Substances 0.000 claims description 60
• 229920000768 polyamine Polymers 0.000 claims description 59
• 238000006243 chemical reaction Methods 0.000 claims description 44
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 43
• 150000002430 hydrocarbons Chemical group 0.000 claims description 43
• 239000012530 fluid Substances 0.000 claims description 39
• 239000003795 chemical substances by application Substances 0.000 claims description 37
• 229930195733 hydrocarbon Natural products 0.000 claims description 37
• 229910052757 nitrogen Inorganic materials 0.000 claims description 37
• 239000002562 thickening agent Substances 0.000 claims description 34
• 239000004215 Carbon black (E152) Substances 0.000 claims description 33
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 33
• 125000001931 aliphatic group Chemical group 0.000 claims description 31
• 125000003118 aryl group Chemical group 0.000 claims description 31
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 30
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 29
• 125000000217 alkyl group Chemical group 0.000 claims description 29
• 150000001735 carboxylic acids Chemical class 0.000 claims description 28
• 125000002947 alkylene group Chemical group 0.000 claims description 27
• 150000001875 compounds Chemical class 0.000 claims description 26
• 125000000623 heterocyclic group Chemical group 0.000 claims description 23
• 150000003839 salts Chemical class 0.000 claims description 23
• AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 22
• 150000003141 primary amines Chemical class 0.000 claims description 21
• 150000003335 secondary amines Chemical class 0.000 claims description 21
• 239000013538 functional additive Substances 0.000 claims description 19
• 239000004094 surface-active agent Substances 0.000 claims description 18
• 229910021529 ammonia Inorganic materials 0.000 claims description 15
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
• 125000005702 oxyalkylene group Chemical class 0.000 claims description 15
• 239000003112 inhibitor Substances 0.000 claims description 14
• OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 13
• 239000001257 hydrogen Substances 0.000 claims description 13
• 229910052739 hydrogen Inorganic materials 0.000 claims description 13
• HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 12
• 229910052751 metal Inorganic materials 0.000 claims description 12
• 239000002184 metal Substances 0.000 claims description 12
• 229920001281 polyalkylene Polymers 0.000 claims description 12
• 150000001340 alkali metals Chemical class 0.000 claims description 11
• 125000003342 alkenyl group Chemical group 0.000 claims description 11
• 150000007942 carboxylates Chemical class 0.000 claims description 11
• 239000000376 reactant Substances 0.000 claims description 11
• 229910052783 alkali metal Inorganic materials 0.000 claims description 10
• 150000005846 sugar alcohols Polymers 0.000 claims description 10
• FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims description 9
• VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 9
• 229910052799 carbon Inorganic materials 0.000 claims description 9
• KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical class OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 9
• 229940014800 succinic anhydride Drugs 0.000 claims description 9
• 150000003512 tertiary amines Chemical class 0.000 claims description 9
• BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical group CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims description 8
• 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 8
• 150000001342 alkaline earth metals Chemical class 0.000 claims description 8
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
• 239000007795 chemical reaction product Substances 0.000 claims description 8
• 239000002270 dispersing agent Substances 0.000 claims description 8
• IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 claims description 8
• 239000003945 anionic surfactant Substances 0.000 claims description 7
• 239000003093 cationic surfactant Substances 0.000 claims description 7
• 229920005862 polyol Polymers 0.000 claims description 7
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
• 150000001339 alkali metal compounds Chemical class 0.000 claims description 6
• 238000005260 corrosion Methods 0.000 claims description 6
• 230000007797 corrosion Effects 0.000 claims description 6
• 239000002736 nonionic surfactant Substances 0.000 claims description 6
• 150000003077 polyols Chemical class 0.000 claims description 6
• 150000001341 alkaline earth metal compounds Chemical class 0.000 claims description 5
• 125000006353 oxyethylene group Chemical group 0.000 claims description 5
• 150000001491 aromatic compounds Chemical class 0.000 claims description 4
• 239000000417 fungicide Substances 0.000 claims description 4
• 150000002429 hydrazines Chemical class 0.000 claims description 4
• 239000001384 succinic acid Substances 0.000 claims description 4
• 239000002280 amphoteric surfactant Substances 0.000 claims description 3
• 125000000962 organic group Chemical group 0.000 claims description 3
• 229920002367 Polyisobutene Polymers 0.000 claims description 2
• 230000000855 fungicidal effect Effects 0.000 claims description 2
• 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 1
• 239000000047 product Substances 0.000 description 40
• LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 39
• 125000001183 hydrocarbyl group Chemical group 0.000 description 38
• 238000000034 method Methods 0.000 description 35
• 150000001298 alcohols Chemical class 0.000 description 33
• 229920000098 polyolefin Polymers 0.000 description 31
• 150000001732 carboxylic acid derivatives Chemical class 0.000 description 30
• 239000012141 concentrate Substances 0.000 description 27
• 229910052801 chlorine Inorganic materials 0.000 description 23
• 239000000460 chlorine Substances 0.000 description 22
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 20
• 150000002148 esters Chemical class 0.000 description 20
• 239000000126 substance Substances 0.000 description 20
• 239000000654 additive Substances 0.000 description 18
• 229920000642 polymer Polymers 0.000 description 18
• GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 17
• 239000007788 liquid Substances 0.000 description 17
• MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 16
• 150000001336 alkenes Chemical class 0.000 description 15
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 14
• 239000003921 oil Substances 0.000 description 14
• 235000019198 oils Nutrition 0.000 description 14
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 13
• 150000001408 amides Chemical class 0.000 description 13
• 239000003153 chemical reaction reagent Substances 0.000 description 13
• 230000008569 process Effects 0.000 description 13
• 239000005977 Ethylene Substances 0.000 description 12
• 239000012445 acidic reagent Substances 0.000 description 12
• 150000007513 acids Chemical class 0.000 description 12
• 238000000354 decomposition reaction Methods 0.000 description 12
• 239000002904 solvent Substances 0.000 description 12
• VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 11
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 11
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 11
• GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 11
• 239000003085 diluting agent Substances 0.000 description 11
• WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 11
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
• 125000001424 substituent group Chemical group 0.000 description 11
• 239000000178 monomer Substances 0.000 description 10
• PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 9
• 238000007792 addition Methods 0.000 description 9
• 150000004982 aromatic amines Chemical group 0.000 description 9
• ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 9
• 229940012017 ethylenediamine Drugs 0.000 description 9
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
• 238000005660 chlorination reaction Methods 0.000 description 8
• 239000006185 dispersion Substances 0.000 description 8
• JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 8
• 229920006395 saturated elastomer Polymers 0.000 description 8
• 229910052717 sulfur Inorganic materials 0.000 description 8
• 239000011593 sulfur Substances 0.000 description 8
• RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 7
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 7
• 125000003277 amino group Chemical group 0.000 description 7
• RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
• 239000000543 intermediate Substances 0.000 description 7
• 239000000314 lubricant Substances 0.000 description 7
• 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
• 239000000243 solution Substances 0.000 description 7
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical class C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
• NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 6
• QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 6
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
• PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
• 125000003545 alkoxy group Chemical group 0.000 description 6
• 239000008346 aqueous phase Substances 0.000 description 6
• 125000004429 atom Chemical group 0.000 description 6
• 238000009833 condensation Methods 0.000 description 6
• 230000005494 condensation Effects 0.000 description 6
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 6
• 125000004433 nitrogen atom Chemical group N* 0.000 description 6
• 150000002989 phenols Chemical class 0.000 description 6
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 6
• 235000011044 succinic acid Nutrition 0.000 description 6
• 230000008719 thickening Effects 0.000 description 6
• VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 5
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 5
• RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 5
• 230000000996 additive effect Effects 0.000 description 5
• 125000002723 alicyclic group Chemical group 0.000 description 5
• 150000001721 carbon Chemical class 0.000 description 5
• 239000003925 fat Substances 0.000 description 5
• 125000005842 heteroatom Chemical group 0.000 description 5
• 229920001519 homopolymer Polymers 0.000 description 5
• PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 4
• 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 4
• 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 4
• 239000004386 Erythritol Substances 0.000 description 4
• UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 4
• 230000029936 alkylation Effects 0.000 description 4
• 238000005804 alkylation reaction Methods 0.000 description 4
• XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 4
• 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
• 239000002585 base Substances 0.000 description 4
• 150000001720 carbohydrates Chemical class 0.000 description 4
• 235000014633 carbohydrates Nutrition 0.000 description 4
• 229920002678 cellulose Polymers 0.000 description 4
• 125000001309 chloro group Chemical group Cl* 0.000 description 4
• 125000004122 cyclic group Chemical group 0.000 description 4
• PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 4
• 150000004985 diamines Chemical class 0.000 description 4
• POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 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
• 235000019414 erythritol Nutrition 0.000 description 4
• 239000004615 ingredient Substances 0.000 description 4
• JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 4
• 229910052760 oxygen Inorganic materials 0.000 description 4
• 239000001301 oxygen Substances 0.000 description 4
• 238000006116 polymerization reaction Methods 0.000 description 4
• 239000011541 reaction mixture Substances 0.000 description 4
• JWHOQZUREKYPBY-UHFFFAOYSA-N rubonic acid Natural products CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CC(=O)C34C)C2C1)C(=O)O JWHOQZUREKYPBY-UHFFFAOYSA-N 0.000 description 4
• 239000000600 sorbitol Substances 0.000 description 4
• 238000003756 stirring Methods 0.000 description 4
• 238000006467 substitution reaction Methods 0.000 description 4
• 125000003396 thiol group Chemical class [H]S* 0.000 description 4
• 239000004711 α-olefin Substances 0.000 description 4
• KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 3
• MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 3
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
• OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
• 208000000474 Poliomyelitis Diseases 0.000 description 3
• ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
• DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
• 235000021355 Stearic acid Nutrition 0.000 description 3
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
• 230000001476 alcoholic effect Effects 0.000 description 3
• 125000003710 aryl alkyl group Chemical group 0.000 description 3
• 239000011203 carbon fibre reinforced carbon Substances 0.000 description 3
• 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 3
• 239000001913 cellulose Substances 0.000 description 3
• 235000010980 cellulose Nutrition 0.000 description 3
• 239000007859 condensation product Substances 0.000 description 3
• 239000004020 conductor Substances 0.000 description 3
• 235000014113 dietary fatty acids Nutrition 0.000 description 3
• 238000007865 diluting Methods 0.000 description 3
• NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical compound OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 3
• 238000005516 engineering process Methods 0.000 description 3
• 150000002170 ethers Chemical class 0.000 description 3
• 239000000194 fatty acid Substances 0.000 description 3
• 229930195729 fatty acid Natural products 0.000 description 3
• 150000004665 fatty acids Chemical class 0.000 description 3
• 150000004676 glycans Chemical class 0.000 description 3
• 150000002334 glycols Chemical class 0.000 description 3
• 238000010438 heat treatment Methods 0.000 description 3
• 239000002563 ionic surfactant Substances 0.000 description 3
• 239000004816 latex Substances 0.000 description 3
• 229920000126 latex Polymers 0.000 description 3
• 238000005461 lubrication Methods 0.000 description 3
• FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
• 239000000463 material Substances 0.000 description 3
• QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
• QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
• OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
• OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 3
• 229910052698 phosphorus Inorganic materials 0.000 description 3
• 239000011574 phosphorus Substances 0.000 description 3
• 229920001282 polysaccharide Polymers 0.000 description 3
• 239000005017 polysaccharide Substances 0.000 description 3
• 238000002360 preparation method Methods 0.000 description 3
• 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 3
• 230000001568 sexual effect Effects 0.000 description 3
• 239000008117 stearic acid Substances 0.000 description 3
• 150000003444 succinic acids Chemical class 0.000 description 3
• 235000000346 sugar Nutrition 0.000 description 3
• 125000001302 tertiary amino group Chemical group 0.000 description 3
• WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
• OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
• RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 2
• ARXKVVRQIIOZGF-UHFFFAOYSA-N 1,2,4-butanetriol Chemical compound OCCC(O)CO ARXKVVRQIIOZGF-UHFFFAOYSA-N 0.000 description 2
• VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-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
• CYOIAXUAIXVWMU-UHFFFAOYSA-N 2-[2-aminoethyl(2-hydroxyethyl)amino]ethanol Chemical compound NCCN(CCO)CCO CYOIAXUAIXVWMU-UHFFFAOYSA-N 0.000 description 2
• JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 2
• KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
• JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
• WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
• WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 description 2
• LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
• FRDAATYAJDYRNW-UHFFFAOYSA-N 3-methyl-3-pentanol Chemical class CCC(C)(O)CC FRDAATYAJDYRNW-UHFFFAOYSA-N 0.000 description 2
• KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
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• UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
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