BE607421A

BE607421A -

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Publication number: BE607421A
Authority: BE; Belgium
Prior art keywords: sep; layer; developing; dyes; dye
Prior art date

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English (en)

French (fr)

Publication of BE607421A publication Critical patent/BE607421A/fr

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239000000975 dye Substances 0.000 claims description 176
-1 silver halides Chemical class 0.000 claims description 89
239000000839 emulsion Substances 0.000 claims description 75
229910052709 silver Inorganic materials 0.000 claims description 61
239000004332 silver Substances 0.000 claims description 61
239000007788 liquid Substances 0.000 claims description 43
238000000034 method Methods 0.000 claims description 42
150000001875 compounds Chemical class 0.000 claims description 39
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 claims description 38
230000008569 process Effects 0.000 claims description 35
239000000243 solution Substances 0.000 claims description 33
238000011161 development Methods 0.000 claims description 30
150000004010 onium ions Chemical class 0.000 claims description 27
238000012545 processing Methods 0.000 claims description 22
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 21
238000012546 transfer Methods 0.000 claims description 19
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 14
239000012670 alkaline solution Substances 0.000 claims description 13
230000035945 sensitivity Effects 0.000 claims description 10
238000009792 diffusion process Methods 0.000 claims description 9
PLXMOAALOJOTIY-FPTXNFDTSA-N Aesculin Natural products OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1Oc2cc3C=CC(=O)Oc3cc2O PLXMOAALOJOTIY-FPTXNFDTSA-N 0.000 claims description 8
XCZKKZXWDBOGPA-UHFFFAOYSA-N 2-phenylbenzene-1,4-diol Chemical compound OC1=CC=C(O)C(C=2C=CC=CC=2)=C1 XCZKKZXWDBOGPA-UHFFFAOYSA-N 0.000 claims description 6
125000001453 quaternary ammonium group Chemical group 0.000 claims description 5
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 4
125000005496 phosphonium group Chemical group 0.000 claims description 3
RAGITMCWNGHCHV-UHFFFAOYSA-N 2,5-diphenylbenzene-1,4-diol 2,3,5,6-tetrachlorobenzene-1,4-diol Chemical compound C1(=CC=CC=C1)C1=C(O)C=C(C(=C1)O)C1=CC=CC=C1.ClC1=C(C(=C(C(=C1O)Cl)Cl)O)Cl RAGITMCWNGHCHV-UHFFFAOYSA-N 0.000 claims description 2
SNWSZCGYPHRJEY-UHFFFAOYSA-N 2-cyclohexylbenzene-1,4-diol Chemical compound OC1=CC=C(O)C(C2CCCCC2)=C1 SNWSZCGYPHRJEY-UHFFFAOYSA-N 0.000 claims description 2
ZNQOWAYHQGMKBF-UHFFFAOYSA-N 2-dodecylbenzene-1,4-diol Chemical compound CCCCCCCCCCCCC1=CC(O)=CC=C1O ZNQOWAYHQGMKBF-UHFFFAOYSA-N 0.000 claims description 2
NTKLFSYUWYPMCJ-UHFFFAOYSA-N 2-phenoxybenzene-1,4-diol Chemical compound OC1=CC=C(O)C(OC=2C=CC=CC=2)=C1 NTKLFSYUWYPMCJ-UHFFFAOYSA-N 0.000 claims description 2
IYPWHXGGZZQMMR-UHFFFAOYSA-N C(C)(C)C1=C(O)C=C(C(=C1)O)C(C)C.ClC1=C(O)C=C(C(=C1)O)Cl.C(CCC)C1=C(O)C=CC(=C1)O Chemical compound C(C)(C)C1=C(O)C=C(C(=C1)O)C(C)C.ClC1=C(O)C=C(C(=C1)O)Cl.C(CCC)C1=C(O)C=CC(=C1)O IYPWHXGGZZQMMR-UHFFFAOYSA-N 0.000 claims 1
UNZXQHFIGPGWIA-UHFFFAOYSA-N C(CCC)OC1=C(O)C=C(C(=C1)O)OCCCC.COC1=C(O)C=C(C(=C1)O)OC Chemical compound C(CCC)OC1=C(O)C=C(C(=C1)O)OCCCC.COC1=C(O)C=C(C(=C1)O)OC UNZXQHFIGPGWIA-UHFFFAOYSA-N 0.000 claims 1
UMSPLPDSKMYHNL-UHFFFAOYSA-N NC1=CC=C(C=C1)CCC1=C(O)C=C(C(=C1)O)C.NC1=CC=C(C=C1)CCC1=C(O)C=C(C(=C1)O)Br Chemical compound NC1=CC=C(C=C1)CCC1=C(O)C=C(C(=C1)O)C.NC1=CC=C(C=C1)CCC1=C(O)C=C(C(=C1)O)Br UMSPLPDSKMYHNL-UHFFFAOYSA-N 0.000 claims 1
PCILLCXFKWDRMK-UHFFFAOYSA-N naphthalene-1,4-diol Chemical compound C1=CC=C2C(O)=CC=C(O)C2=C1 PCILLCXFKWDRMK-UHFFFAOYSA-N 0.000 claims 1
239000010410 layer Substances 0.000 description 161
239000000047 product Substances 0.000 description 74
239000012190 activator Substances 0.000 description 39
108010010803 Gelatin Proteins 0.000 description 32
239000008273 gelatin Substances 0.000 description 31
229940014259 gelatin Drugs 0.000 description 31
235000019322 gelatine Nutrition 0.000 description 31
235000011852 gelatine desserts Nutrition 0.000 description 31
229920000159 gelatin Polymers 0.000 description 30
239000000463 material Substances 0.000 description 24
239000002904 solvent Substances 0.000 description 21
238000012360 testing method Methods 0.000 description 20
150000003839 salts Chemical class 0.000 description 19
239000000203 mixture Substances 0.000 description 18
239000000084 colloidal system Substances 0.000 description 15
230000000694 effects Effects 0.000 description 14
125000000217 alkyl group Chemical group 0.000 description 13
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
239000003086 colorant Substances 0.000 description 12
238000011109 contamination Methods 0.000 description 12
150000003254 radicals Chemical class 0.000 description 12
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 11
239000006185 dispersion Substances 0.000 description 11
230000006872 improvement Effects 0.000 description 11
230000002829 reductive effect Effects 0.000 description 11
230000009471 action Effects 0.000 description 10
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 9
125000003118 aryl group Chemical group 0.000 description 9
239000011230 binding agent Substances 0.000 description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
150000003242 quaternary ammonium salts Chemical class 0.000 description 9
238000009835 boiling Methods 0.000 description 8
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 8
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 7
239000007864 aqueous solution Substances 0.000 description 7
239000002585 base Substances 0.000 description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
150000001450 anions Chemical class 0.000 description 6
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
150000004820 halides Chemical class 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 6
230000003647 oxidation Effects 0.000 description 6
238000007254 oxidation reaction Methods 0.000 description 6
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 5
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 5
239000004372 Polyvinyl alcohol Substances 0.000 description 5
239000002253 acid Substances 0.000 description 5
125000004429 atom Chemical group 0.000 description 5
229920002678 cellulose Polymers 0.000 description 5
238000004040 coloring Methods 0.000 description 5
125000000623 heterocyclic group Chemical group 0.000 description 5
229920002451 polyvinyl alcohol Polymers 0.000 description 5
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 5
235000019345 sodium thiosulphate Nutrition 0.000 description 5
239000000126 substance Substances 0.000 description 5
125000001424 substituent group Chemical group 0.000 description 5
JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 5
VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
230000010933 acylation Effects 0.000 description 4
238000005917 acylation reaction Methods 0.000 description 4
125000002947 alkylene group Chemical group 0.000 description 4
150000004056 anthraquinones Chemical class 0.000 description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
230000007935 neutral effect Effects 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 3
ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 3
ABFDKXBSQCTIKH-UHFFFAOYSA-M 1-ethylpyridin-1-ium;bromide Chemical compound [Br-].CC[N+]1=CC=CC=C1 ABFDKXBSQCTIKH-UHFFFAOYSA-M 0.000 description 3
CUZKCNWZBXLAJX-UHFFFAOYSA-N 2-phenylmethoxyethanol Chemical compound OCCOCC1=CC=CC=C1 CUZKCNWZBXLAJX-UHFFFAOYSA-N 0.000 description 3
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
239000004354 Hydroxyethyl cellulose Substances 0.000 description 3
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 3
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 3
239000003513 alkali Substances 0.000 description 3
125000003545 alkoxy group Chemical group 0.000 description 3
239000001913 cellulose Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
230000000295 complement effect Effects 0.000 description 3
238000010586 diagram Methods 0.000 description 3
238000001035 drying Methods 0.000 description 3
XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
125000005843 halogen group Chemical group 0.000 description 3
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 3
239000003112 inhibitor Substances 0.000 description 3
230000009467 reduction Effects 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 2
LKGFNNSOZPTLSS-UHFFFAOYSA-M 1-benzyl-2-methylpyridin-1-ium;bromide Chemical compound [Br-].CC1=CC=CC=[N+]1CC1=CC=CC=C1 LKGFNNSOZPTLSS-UHFFFAOYSA-M 0.000 description 2
WXTMDXOMEHJXQO-UHFFFAOYSA-N 2,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC=C1O WXTMDXOMEHJXQO-UHFFFAOYSA-N 0.000 description 2
XPAZGLFMMUODDK-UHFFFAOYSA-N 6-nitro-1h-benzimidazole Chemical compound [O-][N+](=O)C1=CC=C2N=CNC2=C1 XPAZGLFMMUODDK-UHFFFAOYSA-N 0.000 description 2
DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 2
229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 2
BHJHPYFAYGAPLS-UHFFFAOYSA-N Guaicyl acetate Chemical compound COC1=CC=CC=C1OC(C)=O BHJHPYFAYGAPLS-UHFFFAOYSA-N 0.000 description 2
AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical class N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 2
125000003282 alkyl amino group Chemical group 0.000 description 2
MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
125000004104 aryloxy group Chemical group 0.000 description 2
CREXVNNSNOKDHW-UHFFFAOYSA-N azaniumylideneazanide Chemical group N[N] CREXVNNSNOKDHW-UHFFFAOYSA-N 0.000 description 2
230000008901 benefit Effects 0.000 description 2
WZJYKHNJTSNBHV-UHFFFAOYSA-N benzo[h]quinoline Chemical class C1=CN=C2C3=CC=CC=C3C=CC2=C1 WZJYKHNJTSNBHV-UHFFFAOYSA-N 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
239000002775 capsule Substances 0.000 description 2
150000001720 carbohydrates Chemical class 0.000 description 2
125000005518 carboxamido 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
238000006243 chemical reaction Methods 0.000 description 2
239000011248 coating agent Substances 0.000 description 2
238000000576 coating method Methods 0.000 description 2
229960002380 dibutyl phthalate Drugs 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 2
230000001747 exhibiting effect Effects 0.000 description 2
238000001914 filtration Methods 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
IGMNYECMUMZDDF-UHFFFAOYSA-N homogentisic acid Chemical compound OC(=O)CC1=CC(O)=CC=C1O IGMNYECMUMZDDF-UHFFFAOYSA-N 0.000 description 2
239000011229 interlayer Substances 0.000 description 2
AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical class C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
150000002596 lactones Chemical class 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
MQWCXKGKQLNYQG-UHFFFAOYSA-N methyl cyclohexan-4-ol Natural products CC1CCC(O)CC1 MQWCXKGKQLNYQG-UHFFFAOYSA-N 0.000 description 2
QRWZCJXEAOZAAW-UHFFFAOYSA-N n,n,2-trimethylprop-2-enamide Chemical compound CN(C)C(=O)C(C)=C QRWZCJXEAOZAAW-UHFFFAOYSA-N 0.000 description 2
ZWDZJRRQSXLOQR-UHFFFAOYSA-N n-butyl-n-phenylacetamide Chemical compound CCCCN(C(C)=O)C1=CC=CC=C1 ZWDZJRRQSXLOQR-UHFFFAOYSA-N 0.000 description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
230000003071 parasitic effect Effects 0.000 description 2
239000002245 particle Substances 0.000 description 2
CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 2
229920002689 polyvinyl acetate Polymers 0.000 description 2
239000011118 polyvinyl acetate Substances 0.000 description 2
229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
108090000623 proteins and genes Proteins 0.000 description 2
150000004023 quaternary phosphonium compounds Chemical class 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 2
230000003595 spectral effect Effects 0.000 description 2
239000000758 substrate Substances 0.000 description 2
125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 2
LUMLZKVIXLWTCI-NSCUHMNNSA-N (e)-2,3-dichloro-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(/Cl)C=O LUMLZKVIXLWTCI-NSCUHMNNSA-N 0.000 description 1
SGWDPXMORNZDKZ-UHFFFAOYSA-N 1,2-dibenzylpyridin-1-ium Chemical compound C=1C=CC=[N+](CC=2C=CC=CC=2)C=1CC1=CC=CC=C1 SGWDPXMORNZDKZ-UHFFFAOYSA-N 0.000 description 1
AIGNCQCMONAWOL-UHFFFAOYSA-N 1,3-benzoselenazole Chemical class C1=CC=C2[se]C=NC2=C1 AIGNCQCMONAWOL-UHFFFAOYSA-N 0.000 description 1
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
XXOFSLDVRYQVSV-UHFFFAOYSA-N 1,4-bis(2-aminoethylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(NCCN)=CC=C2NCCN XXOFSLDVRYQVSV-UHFFFAOYSA-N 0.000 description 1
MGMFSGVTTUUFOE-UHFFFAOYSA-N 1-(2-phenylethyl)pyridin-1-ium Chemical compound C=1C=CC=CC=1CC[N+]1=CC=CC=C1 MGMFSGVTTUUFOE-UHFFFAOYSA-N 0.000 description 1
JHPZVPVIEQJNSU-UHFFFAOYSA-M 1-ethyl-2-methyl-3-(2-phenylethyl)benzimidazol-3-ium;bromide Chemical compound [Br-].C12=CC=CC=C2N(CC)C(C)=[N+]1CCC1=CC=CC=C1 JHPZVPVIEQJNSU-UHFFFAOYSA-M 0.000 description 1
DPNHYAUITGEXCI-UHFFFAOYSA-M 1-heptyl-2-methylpyridin-1-ium;bromide Chemical compound [Br-].CCCCCCC[N+]1=CC=CC=C1C DPNHYAUITGEXCI-UHFFFAOYSA-M 0.000 description 1
NEQDNPLLVJBQNJ-UHFFFAOYSA-N 1-pentylpyrrolidine-2,5-dione Chemical compound CCCCCN1C(=O)CCC1=O NEQDNPLLVJBQNJ-UHFFFAOYSA-N 0.000 description 1
FGQSEPCQVURWHV-UHFFFAOYSA-N 1-piperidin-1-yldodecan-1-one Chemical compound CCCCCCCCCCCC(=O)N1CCCCC1 FGQSEPCQVURWHV-UHFFFAOYSA-N 0.000 description 1
OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical class C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
JAAIPIWKKXCNOC-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-thiolate Chemical class SC1=NN=NN1 JAAIPIWKKXCNOC-UHFFFAOYSA-N 0.000 description 1
YSOKMOXAGMIZFZ-UHFFFAOYSA-N 2,4-dinitrophenetole Chemical compound CCOC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O YSOKMOXAGMIZFZ-UHFFFAOYSA-N 0.000 description 1
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