SE185976C1

SE185976C1 -

Info

Publication number: SE185976C1
Authority: SE; Sweden
Prior art keywords: bis; set according; oil; proportion; carbon atoms
Prior art date: 1963-01-01

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Other languages

English (en)

Swedish (sv)

Publication date

1963-01-01

1963-01-01 Publication of SE185976C1 publication Critical patent/SE185976C1/sv

Links

-1 cationic radicals Chemical class 0.000 claims description 34
239000000654 additive Substances 0.000 claims description 22
239000003921 oil Substances 0.000 claims description 21
125000000217 alkyl group Chemical group 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 10
150000002148 esters Chemical class 0.000 claims description 9
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
APCAAVOBFGAQFD-UHFFFAOYSA-N (phosphonomethyldisulfanyl)methylphosphonic acid Chemical compound OP(O)(=O)CSSCP(O)(O)=O APCAAVOBFGAQFD-UHFFFAOYSA-N 0.000 claims description 7
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 7
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 4
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
150000003254 radicals Chemical class 0.000 claims description 4
150000003839 salts Chemical class 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
125000004434 sulfur atom Chemical group 0.000 claims description 3
YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
229910052698 phosphorus Inorganic materials 0.000 claims description 2
150000003335 secondary amines Chemical class 0.000 claims description 2
150000003141 primary amines Chemical class 0.000 claims 2
229920000742 Cotton Polymers 0.000 claims 1
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
150000003973 alkyl amines Chemical group 0.000 claims 1
150000001723 carbon free-radicals Chemical class 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
239000010688 mineral lubricating oil Substances 0.000 claims 1
230000004048 modification Effects 0.000 claims 1
238000012986 modification Methods 0.000 claims 1
239000011574 phosphorus Substances 0.000 claims 1
239000000203 mixture Substances 0.000 description 23
239000002480 mineral oil Substances 0.000 description 21
230000000996 additive effect Effects 0.000 description 18
235000010446 mineral oil Nutrition 0.000 description 12
VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 9
229930195733 hydrocarbon Natural products 0.000 description 8
150000001875 compounds Chemical class 0.000 description 7
239000004215 Carbon black (E152) Substances 0.000 description 6
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 6
150000002430 hydrocarbons Chemical class 0.000 description 6
MDWVSAYEQPLWMX-UHFFFAOYSA-N 4,4'-Methylenebis(2,6-di-tert-butylphenol) Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 MDWVSAYEQPLWMX-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 4
229930185605 Bisphenol Natural products 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
BPHNRQYTEGQWFG-UHFFFAOYSA-N butoxy-[[[butoxy(hydroxy)phosphoryl]methyldisulfanyl]methyl]phosphinic acid Chemical compound C(CCC)OP(=O)(O)CSSCP(=O)(OCCCC)O BPHNRQYTEGQWFG-UHFFFAOYSA-N 0.000 description 3
239000007795 chemical reaction product Substances 0.000 description 3
239000010779 crude oil Substances 0.000 description 3
239000000295 fuel oil Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
239000000047 product Substances 0.000 description 3
238000007670 refining Methods 0.000 description 3
238000010992 reflux Methods 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
229910052717 sulfur Inorganic materials 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
NPNBLTJGRBYCJB-UHFFFAOYSA-N 1-[butoxy(methyl)phosphoryl]oxybutane Chemical compound CCCCOP(C)(=O)OCCCC NPNBLTJGRBYCJB-UHFFFAOYSA-N 0.000 description 2
SAIKULLUBZKPDA-UHFFFAOYSA-N Bis(2-ethylhexyl) amine Chemical compound CCCCC(CC)CNCC(CC)CCCC SAIKULLUBZKPDA-UHFFFAOYSA-N 0.000 description 2
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
LTJSXGVQCAVSJW-UHFFFAOYSA-N [K+].[K+].[S-][S-] Chemical compound [K+].[K+].[S-][S-] LTJSXGVQCAVSJW-UHFFFAOYSA-N 0.000 description 2
FLPSWUXKDMMXBJ-UHFFFAOYSA-N [chloromethyl(cyclohexyloxy)phosphoryl]oxycyclohexane Chemical compound ClCP(OC1CCCCC1)(OC1CCCCC1)=O FLPSWUXKDMMXBJ-UHFFFAOYSA-N 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
MOFCYHDQWIZKMY-UHFFFAOYSA-N chloromethylphosphonic acid Chemical compound OP(O)(=O)CCl MOFCYHDQWIZKMY-UHFFFAOYSA-N 0.000 description 2
230000008878 coupling Effects 0.000 description 2
238000010168 coupling process Methods 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical group CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 description 2
HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
230000001050 lubricating effect Effects 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
235000011007 phosphoric acid Nutrition 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
150000003018 phosphorus compounds Chemical class 0.000 description 2
238000006748 scratching Methods 0.000 description 2
230000002393 scratching effect Effects 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000001384 succinic acid Substances 0.000 description 2
125000000446 sulfanediyl group Chemical group *S* 0.000 description 2
239000011593 sulfur Substances 0.000 description 2
OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
ZJEHRMYJNACSLL-UHFFFAOYSA-N 1-[butoxy(chloro)phosphoryl]oxybutane Chemical compound CCCCOP(Cl)(=O)OCCCC ZJEHRMYJNACSLL-UHFFFAOYSA-N 0.000 description 1
LSGPZYLAHPLSBS-UHFFFAOYSA-N 1-[butoxy(chloromethyl)phosphoryl]oxybutane Chemical compound CCCCOP(=O)(CCl)OCCCC LSGPZYLAHPLSBS-UHFFFAOYSA-N 0.000 description 1
SUGMXDMMEJYWBB-UHFFFAOYSA-N 1-[butoxy(trichloromethyl)phosphoryl]oxybutane Chemical compound CCCCOP(=O)(C(Cl)(Cl)Cl)OCCCC SUGMXDMMEJYWBB-UHFFFAOYSA-N 0.000 description 1
VGVQCWXTNOGLIV-UHFFFAOYSA-N 1-[butoxy-[(dibutoxyphosphorylmethyldisulfanyl)methyl]phosphoryl]oxybutane Chemical compound C(CCC)OP(=O)(OCCCC)CSSCP(=O)(OCCCC)OCCCC VGVQCWXTNOGLIV-UHFFFAOYSA-N 0.000 description 1
WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical group [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 description 1
RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
JRBAVVHMQRKGLN-UHFFFAOYSA-N 16,16-dimethylheptadecan-1-amine Chemical compound CC(C)(C)CCCCCCCCCCCCCCCN JRBAVVHMQRKGLN-UHFFFAOYSA-N 0.000 description 1
MQCPOLNSJCWPGT-UHFFFAOYSA-N 2,2'-Bisphenol F Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1O MQCPOLNSJCWPGT-UHFFFAOYSA-N 0.000 description 1
OSYHPZSUMUFXHW-UHFFFAOYSA-N 2,3-ditert-butyl-4-[(2,3-ditert-butyl-4-hydroxyphenyl)methyl]phenol Chemical compound CC(C)(C)C1=C(O)C=CC(CC=2C(=C(C(O)=CC=2)C(C)(C)C)C(C)(C)C)=C1C(C)(C)C OSYHPZSUMUFXHW-UHFFFAOYSA-N 0.000 description 1
XOJRBTBFGUKLPU-UHFFFAOYSA-N 2,5-ditert-butyl-4-[(2,5-ditert-butyl-4-hydroxyphenyl)methyl]phenol Chemical compound C1=C(O)C(C(C)(C)C)=CC(CC=2C(=CC(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1C(C)(C)C XOJRBTBFGUKLPU-UHFFFAOYSA-N 0.000 description 1
DQSYGNJXYMAPMV-UHFFFAOYSA-N 2,6-ditert-butyl-4-(3,5-ditert-butyl-4-hydroxyphenyl)sulfanylphenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(SC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 DQSYGNJXYMAPMV-UHFFFAOYSA-N 0.000 description 1
VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
KRQUFUKTQHISJB-YYADALCUSA-N 2-[(E)-N-[2-(4-chlorophenoxy)propoxy]-C-propylcarbonimidoyl]-3-hydroxy-5-(thian-3-yl)cyclohex-2-en-1-one Chemical compound CCC\C(=N/OCC(C)OC1=CC=C(Cl)C=C1)C1=C(O)CC(CC1=O)C1CCCSC1 KRQUFUKTQHISJB-YYADALCUSA-N 0.000 description 1
WQUVEAFXOHYUQN-UHFFFAOYSA-N 2-ethyl-4-[(3-ethyl-4-hydroxyphenyl)disulfanyl]phenol Chemical compound C(C)C=1C=C(C=CC1O)SSC1=CC(=C(C=C1)O)CC WQUVEAFXOHYUQN-UHFFFAOYSA-N 0.000 description 1
LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 1
HXIQYSLFEXIOAV-UHFFFAOYSA-N 2-tert-butyl-4-(5-tert-butyl-4-hydroxy-2-methylphenyl)sulfanyl-5-methylphenol Chemical compound CC1=CC(O)=C(C(C)(C)C)C=C1SC1=CC(C(C)(C)C)=C(O)C=C1C HXIQYSLFEXIOAV-UHFFFAOYSA-N 0.000 description 1
RKLRVTKRKFEVQG-UHFFFAOYSA-N 2-tert-butyl-4-[(3-tert-butyl-4-hydroxy-5-methylphenyl)methyl]-6-methylphenol Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 RKLRVTKRKFEVQG-UHFFFAOYSA-N 0.000 description 1
OWWQFSAOAYMOMP-UHFFFAOYSA-N 2-tert-butyl-4-[(3-tert-butyl-4-hydroxy-5-propan-2-ylphenyl)methyl]-6-propan-2-ylphenol Chemical compound C(C)(C)(C)C=1C=C(C=C(C1O)C(C)C)CC1=CC(=C(C(=C1)C(C)C)O)C(C)(C)C OWWQFSAOAYMOMP-UHFFFAOYSA-N 0.000 description 1
BNEHSVRWDKQOSR-UHFFFAOYSA-N 2-tert-butyl-4-[[3-tert-butyl-4-hydroxy-5-(2,4,4-trimethylpentan-2-yl)phenyl]methyl]-6-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound C(C)(C)(C)C=1C=C(C=C(C1O)C(C)(C)CC(C)(C)C)CC1=CC(=C(C(=C1)C(C)(C)CC(C)(C)C)O)C(C)(C)C BNEHSVRWDKQOSR-UHFFFAOYSA-N 0.000 description 1
MQWCQFCZUNBTCM-UHFFFAOYSA-N 2-tert-butyl-6-(3-tert-butyl-2-hydroxy-5-methylphenyl)sulfanyl-4-methylphenol Chemical compound CC(C)(C)C1=CC(C)=CC(SC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O MQWCQFCZUNBTCM-UHFFFAOYSA-N 0.000 description 1
YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
FVXBXPJANJCDHI-UHFFFAOYSA-N 3-(2,5-dihexyl-3-hydroxyphenyl)sulfanyl-2,5-dihexylphenol Chemical compound C(CCCCC)C1=C(C=C(C=C1O)CCCCCC)SC1=C(C(=CC(=C1)CCCCCC)O)CCCCCC FVXBXPJANJCDHI-UHFFFAOYSA-N 0.000 description 1
KWIQXAVBQDPHCS-UHFFFAOYSA-N 3-[2-[3-hydroxy-2,4-bis(2-methylbutan-2-yl)phenyl]propyl]-2,6-bis(2-methylbutan-2-yl)phenol Chemical compound C(C)(C)(CC)C1=C(C=CC(=C1O)C(C)(C)CC)CC(C)C1=C(C(=C(C=C1)C(C)(C)CC)O)C(C)(C)CC KWIQXAVBQDPHCS-UHFFFAOYSA-N 0.000 description 1
VJGHSPGETLFPHX-UHFFFAOYSA-N 3-hexadecylhexanedioic acid Chemical compound CCCCCCCCCCCCCCCCC(CC(O)=O)CCC(O)=O VJGHSPGETLFPHX-UHFFFAOYSA-N 0.000 description 1
IWYSTJDKCRBQSD-UHFFFAOYSA-N 4-(4-hydroxy-2,5-dipentylphenyl)sulfanyl-2,5-dipentylphenol Chemical compound C1=C(O)C(CCCCC)=CC(SC=2C(=CC(O)=C(CCCCC)C=2)CCCCC)=C1CCCCC IWYSTJDKCRBQSD-UHFFFAOYSA-N 0.000 description 1
MIHFISIBBGHYLX-UHFFFAOYSA-N 4-(4-hydroxy-2,6-dipropylphenoxy)-3,5-dipropylphenol Chemical compound C(CC)C1=C(C(=CC(=C1)O)CCC)OC1=C(C=C(C=C1CCC)O)CCC MIHFISIBBGHYLX-UHFFFAOYSA-N 0.000 description 1
LIDOZHJCZPEWDI-UHFFFAOYSA-N 4-[[4-hydroxy-3,5-bis(2,4,4-trimethylpentan-2-yl)phenyl]methyl]-2,6-bis(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=C(O)C(C(C)(C)CC(C)(C)C)=CC(CC=2C=C(C(O)=C(C=2)C(C)(C)CC(C)(C)C)C(C)(C)CC(C)(C)C)=C1 LIDOZHJCZPEWDI-UHFFFAOYSA-N 0.000 description 1
CSULCRUOKIJXCT-UHFFFAOYSA-N 5-[(3-hydroxy-5-methyl-4-propylphenyl)disulfanyl]-3-methyl-2-propylphenol Chemical compound CC=1C=C(C=C(C1CCC)O)SSC1=CC(=C(C(=C1)O)CCC)C CSULCRUOKIJXCT-UHFFFAOYSA-N 0.000 description 1
HJCNGGKJQATACT-UHFFFAOYSA-N 6-tert-butyl-2-(3-tert-butyl-2-hydroxy-6-methylphenyl)sulfanyl-3-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1SC1=C(C)C=CC(C(C)(C)C)=C1O HJCNGGKJQATACT-UHFFFAOYSA-N 0.000 description 1
208000019901 Anxiety disease Diseases 0.000 description 1
GHQIODJXINGUFE-UHFFFAOYSA-N C(C)(C)(C)C1=CC(=C(C=C1C(C)(C)C)CCC)O Chemical compound C(C)(C)(C)C1=CC(=C(C=C1C(C)(C)C)CCC)O GHQIODJXINGUFE-UHFFFAOYSA-N 0.000 description 1
HNFQWCLIVDLTMC-UHFFFAOYSA-N C(CCC)C1=CC(=CC(C1)(O)CCCC)OC=1C=C(CC(C1)(O)CCCC)CCCC Chemical compound C(CCC)C1=CC(=CC(C1)(O)CCCC)OC=1C=C(CC(C1)(O)CCCC)CCCC HNFQWCLIVDLTMC-UHFFFAOYSA-N 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
239000001293 FEMA 3089 Substances 0.000 description 1
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
229920002367 Polyisobutene Polymers 0.000 description 1
241000220317 Rosa Species 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
WGCJUPJNMGWDAU-UHFFFAOYSA-N [chloromethyl(phenoxy)phosphoryl]oxybenzene Chemical compound C=1C=CC=CC=1OP(=O)(CCl)OC1=CC=CC=C1 WGCJUPJNMGWDAU-UHFFFAOYSA-N 0.000 description 1
238000010306 acid treatment Methods 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
230000036506 anxiety Effects 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 0.000 description 1
238000009835 boiling Methods 0.000 description 1
NATUADLETDTIRZ-UHFFFAOYSA-N butoxy(chloromethyl)phosphinic acid Chemical compound C(CCC)OP(O)(=O)CCl NATUADLETDTIRZ-UHFFFAOYSA-N 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
229910003460 diamond Inorganic materials 0.000 description 1
239000010432 diamond Substances 0.000 description 1
ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
150000002019 disulfides Chemical class 0.000 description 1
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