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F-Term-List

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C09B1/00-1/62 AA AA00
NUMBER OF ANTHRAQUINONE SKELETON 		AA01 AA02
. One anthraquinone skeleton per molecule . Two or more anthraquinone skeletons per molecule
AB AB00
NUMBER OF SUBSTITUENT IN POSITION 1, 4, 5, OR 8 OF ANTHRAQUINONE SKELETON 		AB01 AB02 AB03 AB04 AB05
. No substituent i.e. absence . One substituent . Two substituents . Three substituents . Four substituents
AC AC00
NUMBER OF SUBSTITUENT IN POSITION 2, 3, 6, OR 7 OF ANTHRAQUINONE SKELETON 		AC01 AC02 AC03 AC04 AC05
. No substituent i.e. absence . One substituent . Two substituents . Three substituents . Four substituents
AD AD00
TYPE OF SUBSTITUENT 		AD01 AD02 AD03 AD04 AD06 AD07 AD08 AD09 AD10
. Hydrocarbon radicals . . -R . . -Cy containing groups . . -Ph containing groups including aralkyl groups . Hetero atoms: -X . . Halogen: -hal . . hetero atoms being oxygen . . . Hydroxy groups: OH . . . Image 291)
AD11 AD12 AD13 AD14 AD15 AD16 AD17 AD18 AD19 AD20
. . . . -O-R . . . . -O-Cy containing groups . . . . -O-Ph containing groups . . hetero atoms being sulfur . . . -SH . . . Image 297) . . . . -S-R . . . . -S-Cy containing groups . . . . -S-Ph containing groups . . . -SO2
AD21 AD22 AD23 AD24 AD25 AD26 AD27 AD28 AD29
. . . Sulfonic acids or salts thereof: -SO3H(M) . . hetero atoms being nitrogen . . .-NO -NO2 . . . -NH2 . . . Image 301) . . . . -N-R . . . . -N-Cy containing groups . . . . -N-Ph containing groups . . . Imino groups: (see Image 307) (see Image 308)
AD31 AD32 AD33 AD34 AD35 AD37 AD38
. -Y . . -CN . . Ester groups: (see Image 314) . . Carboxylic acids or salts thereof: -CO2H (M) . . Amido groups: -CONH2 (see Image 317) . Others . . Heterocyclic rings
C09B11/00-11/28 BA BA00
OVERALL STRUCTURE 		BA01 BA02 BA03
. Diarylmethane . Triarylmethane . containing multiple diarylmethane or triarylmethane skeletons per molecule
BB BB00
BASIC SKELETON 		BB01 BB02 BB03 BB04 BB05
. Aryl groups not forming identical condensed rings . Two aryl groups condensed through rings containing central carbon atoms: (see Image 323) . . Two aryl groups condensed through heterocyclic rings containing central carbon atoms: (see Image 325) . . . Heterocyclic rings containing sulfur e.g. thioxanthene rings . . . Heterocyclic rings containing oxygen e.g. xanthene rings
BB11 BB12 BB13 BB14 BB15 BB16
. One aryl group and central carbon atom forming identical condensed rings: (see Image 328) . . Central carbon atom being ring member of sultone ring: (see Image 329) . . Central carbon atom being ring member of lactam rings: (see Image 330) . . Central carbon atom being ring member of lactone rings: (see Image 331) . . . Aryl groups being aromatic heterocyclic rings: (see Image 332) . . . . Aryl groups being aromatic heterocyclic rings containing nitrogen: (see Image 333)
BC BC00
TYPE OF RING BONDING TO CENTRAL CARBON ATOM 		BC01 BC02 BC03 BC04 BC05 BC06 BC07 BC08 BC10
. Ph . Aromatic heterocyclic rings: HAr . . Aromatic heterocyclic rings containing nitrogen . . . Pyridine: (see Image 336) . . . Pyrrole: (see Image 337) . . Aromatic heterocyclic rings containing sulfur . . . Thiophenes: (see Image 338) . . Aromatic heterocyclic rings containing oxygen . Others
BD BD00
CONDENSATION STATE OF AR 		BD01 BD02 BD03 BD04 BD05 BD06 BD07 BD08
. uncondensed . condensed only with carbocyclic rings . . Carbocyclic rings or carbocyclic ring systems containing Ph . condensed with rings containing heterocyclic rings . . Nitrogen-containing heterocyclic rings . . Sulfur-containing heterocyclic rings . . Oxygen-containing heterocyclic rings . . Heterocyclic rings containing both nitrogen and oxygen
BE BE00
SUBSTITUENT OF CENTRAL CARBON ATOM, EXCLUDING BASIC SKELETON 		BE01 BE02 BE03 BE05 BE06 BE07 BE08 BE09
. Hydrocarbon radicals: (see Image 341) . . -R acyclic hydrocarbon radicals . . -Cy containing groups . Hetero atoms: -X . . -OH (see Image 348) . . -SH (see Image 351) . . Image 353) . . -NH2 (see Image 354)
BE11 BE13
. -Y . Others
BF BF00
TYPE OF SUBSTITUENT ON AR 		BF01 BF02 BF03 BF04 BF06 BF07 BF08 BF09 BF10
. Hydrocarbon radicals: (see Image 358) . . -R acyclic hydrocarbon radicals . . -Cy containing groups . . -Ph containing groups including aralkyl groups . Hetero atoms: -X . . Halogen: hal . . hetero atoms being oxygen . . . Hydroxy groups: OH . . . Image 369)
BF11 BF12 BF13 BF14 BF15 BF16 BF17 BF18 BF19 BF20
. . . . -O-R . . . . -O-Cy containing groups . . . . -O-Ph containing groups . . hetero atoms being sulfur . . . -SH . . . Image 377) . . . . -S-R . . . . -S-Cy containing groups . . . . -S-Ph containing groups . . . Image 382)
BF21 BF22 BF23 BF24 BF25 BF26 BF27 BF28 BF29
. . . Sulfonic acids or salts thereof: -SO3H (M) . . hetero atoms being nitrogen . . . -NO -NO2 . . . -NH2 . . . Image 385) . . . . -N-R . . . . -N-Cy containing groups . . . . -N-Ph containing groups . . . Imino groups: Image 392) Image 393)
BF31 BF32 BF33 BF34 BF35 BF37 BF38
. -Y . . -CN . . Ester groups: (see Image 399) . . Carboxylic acids or salts thereof: -CO2H(M) . . Amido groups: -CONH2 (see Image 402) . Others . . Heterocyclic rings
C09B23/00-23/16;57/00 CA CA00
FEATURE OF METHINE CHAIN 		CA01 CA02 CA03 CA04 CA05
. having an odd number of methine groups . having an even number of methine groups . . having two methine groups: (see Image 407) . Branched methine chains . Interrupted methine chains
CB CB00
BONDING GROUP OF METHINE CHAIN 		CB01 CB02 CB03 CB05 CB06 CB07
. Hydrocarbon radicals: (see Image 409) . . -R acyclic hydrocarbon radicals . . -Ph containing groups including aralkyl groups . Nitrogen-containing chains . Heterocyclic rings-containing chains . Others
CC CC00
START OR END POINT OF METHINE CHAIN 		CC01 CC02 CC04 CC05 CC06 CC08 CC10
. Image 417) . . Z being rings . Image 418) . . one Z being a ring and the other being an acyclic radical . . both Zs being rings . carbon bonding to methine chains being ring member . Others
CD CD00
TYPE OF ACYCLIC RADICAL BONDING TO STARTING OR ENDING POINT OF METHINE CHAIN 		CD01 CD02 CD04 CD05 CD07 CD08 CD09 CD10
. Hydrocarbon radicals (see Image 420) . . Image 421) . Hetero atoms: -X . . -NH2 (see Image 422) . -Y . . -CN . . Ester groups: (see Image 426) . . Amido groups: -CONH2 (see Image 429)
CD12
. Others
CE CE00
RING BONDING TO START OR END POINT OF METHINE CHAIN 		CE01 CE02 CE03 CE05 CE06 CE07
. Carbocyclic rings . . Ph . Heterocyclic rings . Condensed rings . . condensed with ring systems consisting of only carbocyclic rings . . condensed with ring systems containing heterocyclic ring
DA DA00
STILBENE-BASED SKELETON 		DA01 DA02 DA03 DA04
. Image 432) . . Image 433) . . . Image 434) . . . Image 435)
DB DB00
TYPE OF SUBSTITUENT ON PHENYL GROUP OF STILBENE SKELETON (HETEROCYCLIC RING CONTAINING GROUP IS NOT CONSIDERED AS SUBSTITUENT IN THIS VIEWPOINT.) 		DB01 DB02 DB03 DB05 DB06 DB07 DB08 DB09 DB10
. Hydrocarbon radicals: (see Image 436) . . Image 437) . . Image 438) . Hetero atoms: -X . . Halogen: hal . . -OH (see Image 439) . . Sulfonic acids: -SO3H (M) . . -NO2 . . -NH2 (see Image 442)
DB12 DB13 DB15
. -Y . . Ester groups: (see Image 446) . Others
DC DC00
GROUP BONDING STILBENE SKELETON AND HETEROCYCLIC RING 		DC01 DC02 DC03
. No bonding groups i.e. direct bonding . -N- . Others
DD DD00
TYPE OF HETEROCYCLIC RING 		DD01 DD02 DD03 DD04 DD05 DD06 DD07 DD08 DD09 DD10
. Heterocyclic rings containing only nitrogen as hetero atoms: (see Image 447) . . containing one nitrogen atom . . . Five-membered rings . . . Six-membered rings . . containing two nitrogen atoms . . . Five-membered rings . . . Six-membered rings . . containing three nitrogen atoms . . . Five-membered rings . . . Six-membered rings
DD11 DD12 DD14 DD15 DD16 DD18 DD19
. Heterocyclic rings containing only sulfur atoms as hetero atoms: (see Image 448) . . Five-membered rings . Heterocyclic rings containing only oxygen atoms as hetero atoms: (see Image 449) . . Five-membered rings . . Six-membered rings . Heterocyclic rings containing nitrogen atoms and sulfur atoms as hetero atoms: (see Image 450) . . Five-membered rings
DD21 DD22 DD23 DD24 DD25 DD26 DD28 DD29 DD30
. Heterocyclic rings containing nitrogen atoms and oxygen atoms as hetero atoms: (see Image 451) . . containing one nitrogen atom and one oxygen atom . . . Five-membered rings . . . Six-membered rings . . containing two nitrogen atoms and one oxygen atom . . . Five-membered rings . Heterocyclic rings having thioxo groups: (see Image 452) . Hetero groups having oxo groups: (see Image 453) . Others
DE DE00
TYPE OF SUBSTITUENT ON HETEROCYCLIC RING (BONDING GROUP BETWEEN BASIC SKELETON AND BASIC SKELETON IS NOT CONSIDERED AS SUBSTITUENT.) 		DE01 DE02 DE03 DE04 DE06 DE07 DE08 DE09 DE10
. Hydrocarbon radicals: (see Image 454) . . -R acyclic hydrocarbon radicals . . -Cy containing groups . . -Ph containing groups including aralkyl groups . Hetero atoms: -X . . Halogen: hal . . hetero atoms being oxygen . . . Hydroxyl groups: OH . . . Image 464)
DE11 DE12 DE13 DE14 DE15 DE16 DE17 DE18 DE19 DE20
. . . . -O-R . . . . -O-Cy containing groups . . . . -O-Ph containing groups . . hetero atoms being sulfur . . . -SH . . . Image 472) . . . . -S-R . . . . -S-Cy containing groups . . . . -S-Ph containing groups . . . Image 477)
DE21 DE22 DE23 DE24 DE25 DE26 DE27 DE28 DE29
. . . Sulfonic acids or salts thereof: -SO3H(M) . . hetero atoms being nitrogen . . . -NO -NO2 . . . -NH2 . . . Image 480) . . . . -N-R . . . . -N-Cy containing groups . . . . -N-Ph containing groups . . . Imino groups: (see Image 486) (see Image 487)
DE31 DE32 DE33 DE34 DE35 DE37 DE38
. -Y . . -CN . . Ester groups: (see Image 493) . . Carboxylic acids or salts thereof: -CO2H (M) . . Amido groups: -CONH2 (see Image 496) . Others . . Heterocyclic rings
C09B57/00 EA EA00
OVERALL STRUCTURE 		EA01 EA03 EA04 EA05 EA06 EA07 EA08 EA09 EA10
. acyclic . containing only carbocyclic rings . . containing only Cy . . containing Ph . . . Condensed Ph . . . Ph-Ph . . . Ph-Z-Ph . . . . Image 499) . . . . Ph-nitrogen containing chain-Ph
EA11 EA12 EA13 EA14 EA15 EA16
. containing heterocyclic rings . . Uncondensed heterocyclic rings . . Condensed heterocyclic rings . . having two or more condensed ring systems . . further containing heterocyclic rings and uncondensed Cy . . further containing heterocyclic rings and uncondensed Ph
C09B1/00-1/02;11/00-11/28;23/00-23/16;57/00;62/00-62/84 FA FA00
USE 		FA01 FA02 FA03 FA04 FA05 FA06 FA07 FA08 FA10
. Dyeing or colouring . . Fluorescent whitening agents . Heat-sensitive materials . Pressure-sensitive materials . Photosensitive materials . . Laser light . for liquid crystals . Indicators . Others
JA JA00
TYPE OF COLOURING MATTER BODY 		JA01 JA02 JA03 JA04 JA05 JA06 JA07 JA08 JA09 JA10
. Monoazo dyes . . both diazo components and couplers being aromatic rings . . both diazo components and couplers being heterocyclic rings . . diazo components being aromatic rings and couplers being heterocyclic rings . . diazo components being heterocyclic rings and couplers being aromatic rings . Disazo dyes . Polyazo dyes . Metal complex salt azo dyes . Anthraquinone dyes . Phthalocyanine dyes
JA11 JA12 JA13 JA14
. Dioxazine dyes . Formazane dyes . Dyes having more than one different types of colouring matter bodies . Other dyes
JB JB00
TYPE OF REACTIVE GROUP 		JB01 JB02 JB03 JB04
. Nitrogen-containing heterocyclic rings . . Triazine . Vinyl sulfones . Other reactive groups
JC JC00
DYE HAVING ONLY ONE REACTIVE GROUP 		JC01 JC02 JC03 JC04 JC05 JC06 JC07 JC08 JC09 JC10
. having only one colouring matter body (Monoazo dye takes precedence.) . having more than one colouring matter bodies (Disazo dye takes precedence.) . . C1-R-C2 . Monoazo dyes . . D-> K-R . . R-D-> K . Disazo dyes . . D1->D2->K type . . . D1->D2->K-R . . . Image 530)
JC11 JC12 JC13 JC14 JC15 JC16 JC17
. . . R-D1->D2->K . . D1->K<-D2 types . . . D1->K<-D2-R . . . Image 534) . . K1<-D->K2 types . . . K1<-D->K2-R . . . Image 537)
JD JD00
DYE HAVING TWO REACTIVE GROUPS 		JD01 JD02 JD03 JD04 JD05 JD06 JD07 JD08 JD09 JD10
. having only one colouring matter body (Monoazo takes precedence.) . . R1-C-R2 . . C-R1-R2 . having more than one colouring matter bodies (Disazo dye takes precedence.) . . C1-R1-C2-R2 . . C1-R1-R2-C2 . Monoazo dyes . . D->K-(Ri)2 . . (Ri)2-D->K . . R1-D->K-R2
JD11 JD12 JD13 JD14 JD15 JD16 JD17 JD18 JD19 JD20
. Disazo dyes . . of D1->D2->K types . . . D1->D2->K-(Ri)2 . . . Image 542) . . . (Ri)2-D1->D2->K . . . Image 543) . . . R1-D1->D2->K-R2 . . . Image 544) . . D1->K<-D2 types . . . D1->K<-D2-(Ri)2
JD21 JD22 JD23 JD24 JD25 JD26 JD27 JD28
. . . Image 545) . . . Image 546) . . . R1-D1->K<-D2-K2 . . of K1<-D->K2 types . . . K1<-D->K2-(Ri)2 . . . Image 547) . . . Image 548) . . . R1-K1<-D->K2-R2
JE JE00
DYE HAVING THREE OR MORE REACTIVE GROUPS 		JE01 JE02 JE03 JE04
. having three reactive groups . . having only one colouring matter body . . having more than one colouring matter bodies including disazo or polyazo . having four or more reactive groups
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