ChemicalBook >> CAS DataBase List >>9,9-Bis(4-aminophenyl)fluorene

9,9-Bis(4-aminophenyl)fluorene

CAS No.
15499-84-0
Chemical Name:
9,9-Bis(4-aminophenyl)fluorene
Synonyms
FDA;BAFL;AKOS BBB/416;Zinc03897005;Anilinefluorene;BIO-FARMA BF003152;TIMTEC-BB SBB008629;9,9-bis(4-aminopheny;bisaminophenylfluorene;Bis(4-aminophenyl)fluorene
CBNumber:
CB9439319
Molecular Formula:
C25H20N2
Molecular Weight:
348.44
MDL Number:
MFCD00039156
MOL File:
15499-84-0.mol
MSDS File:
SDS
Last updated:2024-01-08 21:00:42

9,9-Bis(4-aminophenyl)fluorene Properties

Melting point 237-239 °C (lit.)
Boiling point 535.2±50.0 °C(Predicted)
Density 1.245±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
Water Solubility Insoluble in water
form powder to crystal
pka 4.92±0.10(Predicted)
color White to Almost white
InChI InChI=1S/C25H20N2/c26-19-13-9-17(10-14-19)25(18-11-15-20(27)16-12-18)23-7-3-1-5-21(23)22-6-2-4-8-24(22)25/h1-16H,26-27H2
InChIKey KIFDSGGWDIVQGN-UHFFFAOYSA-N
SMILES C1(C2=CC=C(N)C=C2)(C2=CC=C(N)C=C2)C2=C(C=CC=C2)C2=C1C=CC=C2
CAS DataBase Reference 15499-84-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302+H312+H332-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352+P312-P304+P340+P312-P305+P351+P338
Hazard Codes  Xn,Xi
Risk Statements  20/21/22-36/37
Safety Statements  26-36
WGK Germany  3
HazardClass  IRRITANT
HS Code  29215900
NFPA 704
1
2 0

9,9-Bis(4-aminophenyl)fluorene price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 437913 4,4′-(9-Fluorenylidene)dianiline 99% 15499-84-0 25g $251 2024-03-01 Buy
TCI Chemical B1549 9,9-Bis(4-aminophenyl)fluorene >98.0%(T) 15499-84-0 25g $110 2024-03-01 Buy
TCI Chemical B1549 9,9-Bis(4-aminophenyl)fluorene >98.0%(T) 15499-84-0 100g $330 2024-03-01 Buy
TCI Chemical B2654 9,9-Bis(4-aminophenyl)fluorene (purified by sublimation) >99.0%(HPLC)(T) 15499-84-0 1g $91 2024-03-01 Buy
TRC F591593 4,4''-(9H-Fluorene-9,9-diyl)dianiline 15499-84-0 2.5g $90 2021-12-16 Buy
Product number Packaging Price Buy
437913 25g $251 Buy
B1549 25g $110 Buy
B1549 100g $330 Buy
B2654 1g $91 Buy
F591593 2.5g $90 Buy

9,9-Bis(4-aminophenyl)fluorene Chemical Properties,Uses,Production

Description

9,9-Bis(4-aminophenyl)fluorene (FDA) is a fluorene derivative with two aminophenyl substituents on the 9-position. This compound has partial conjugation and can be utilized as a dopant-free organic hole-transporting material in inverted perovskite solar cells. Due to its diaminophenyl groups, FDA is commonly employed in synthesizing polyimides that possess high thermal and hydrolytic stability for optical fiber light guide coatings. Because the FDA is not fully aromatized, it is chosen to produce thermally stable transparent polyimides. Additionally, the polyimide derived from 9,9-bis(4-aminophenyl)fluorene can be further modified through Friedel-Crafts alkylation on the fluorene moiety, as the polyimide backbone remains chemically stable.

Chemical Properties

White powder

Uses

9,9-bis(4-aminophenyl)fluorene be used for preparation of high-strength material and high-temperature polymers.

Preparation

The synthesis of 9,9-Bis(4-aminophenyl)fluorene can be carried out through the following stepwise procedure:
Prepare the reaction mixture:
Place 3.6 g of fluorenone (20 mmol), 7.2 g of aniline hydrochloride (55.6 mmol), 0.5 g of sodium bisulfite (4.8 mmol), 8.8 mL of aniline (96.4 mmol), and 6 mL of toluene in a 100 mL two-necked flask.
Ensure the reaction is conducted under nitrogen protection.
Add a water separator to the two-necked flask.

Begin the reaction:
Stir the reaction mixture and slowly increase the temperature to 120 °C.
Allow the reaction to continue for 30 minutes.
Separate the green liquid produced in the water separator.

Further reaction at elevated temperature:
Continue the reaction at 120 °C for an additional 3 hours.
Separate the water produced in the water separator.

Increase temperature and maintain reaction:
Slowly raise the temperature to 135 °C.
Keep the reaction at this temperature for 1.5 hours.

Monitor for completion:
Check the water separator for any further production of water.
Cease the reaction when no more water is produced in the water separator.

Cool down and adjust pH:
Allow the reacted material to cool to around 60 ℃.
Add 10 wt% potassium hydroxide solution to the reaction mixture.
Adjust the pH of the mixture to 9.
Stir the solution for 15 minutes while it is still hot.

Filtration and purification:
Filter the solution to remove any solid impurities.
Wash the filter cake with water.
Recrystallize the washed filter cake using 30 mL of toluene.
Filter the recrystallized product to obtain pure rice-white product.

Yield determination:
Weigh the obtained pure product, which should amount to 6.55 g.
Calculate the yield by dividing the obtained mass by the theoretical maximum mass and multiplying by 100%.
The yield of the pure rice-white product should be 94%.

General Description

4,4′-(9-Fluorenylidene)dianiline is a diamine.

References

[1] PHAM H D, GIL-ESCRIG L, FERON K, et al. Boosting inverted perovskite solar cell performance by using 9,9-bis(4-diphenylaminophenyl)fluorene functionalized with triphenylamine as a dopant-free hole transporting material?[J]. Journal of Materials Chemistry A, 2019, 20: 12507-12517. DOI:10.1039/C9TA01681C.
[2] G. SONG C. C. Colorless, heat resistant polyimide films derived from 2,3,3′,4′-biphenyltetracarboxylic dianhydride[J]. IOP Conference Series: Materials Science and Engineering, 2020, 73 1. DOI:10.1088/1757-899X/733/1/012035.
[3] WEI J, YU L, YAN L, et al. Synthesis of 9,9-bis(4-hydroxyphenyl) fluorene catalyzed by bifunctional ionic liquids?[J]. RSC Advances, 2021, 52: 32559-32564. DOI:10.1039/D1RA05967J.
[4] SURASAK SEESUKPHRONRARAK. Synthesis and characterization of 9,9-bis(4-hydroxyphenyl and 4-aminophenyl)dibenzofluorenes: Novel fluorene-based monomers[J]. Journal of Polymer Science Part A: Polymer Chemistry, 2019, 57 24: 2602-2605. DOI:10.1002/pola.29540.
[5] HOU CHIEN CHANG. Synthesis of 9,9-bis(4-aminophenyl)fluorene-based benzoxazine and properties of its high-performance thermoset[J]. Journal of Polymer Science Part A: Polymer Chemistry, 2012, 50 11: 2201-2210. DOI:10.1002/pola.25993.
[6] Patent: CN107892649, 2018, A, . Location in patent: Paragraph 0023-0042
[7] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 23, p. 240
[8] DONGHUI YU. Fluorene-Based Phosphine Oxide Host Materials for Blue Electrophosphorescence: An Effective Strategy for a High Triplet Energy Level[J]. Chemistry - A European Journal, 2011, 17 9: 2592-2596. DOI:10.1002/chem.201003434.

486-25-9
62-53-3
15499-84-0
Synthesis of 9,9-Bis(4-aminophenyl)fluorene from 9-Fluorenone and Aniline

9,9-Bis(4-aminophenyl)fluorene Preparation Products And Raw materials

Global( 316)Suppliers
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View Lastest Price from 9,9-Bis(4-aminophenyl)fluorene manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
4,4'-(9H-fluorene-9,9-diyl)dianiline pictures 2024-03-28 4,4'-(9H-fluorene-9,9-diyl)dianiline
15499-84-0
US $0.00 / kg 25kg 98%-99% Inquiry PNP Biotech Co. Ltd
9,9-Bis(4-aminophenyl)fluorene pictures 2024-01-08 9,9-Bis(4-aminophenyl)fluorene
15499-84-0
US $111.00-1.00 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
9,9-BIS(4-AMINOPHENYL)FLUORENE pictures 2023-07-25 9,9-BIS(4-AMINOPHENYL)FLUORENE
15499-84-0
US $0.00 / kg 1kg 99% 20 tons Hebei Yanxi Chemical Co., Ltd.
BenzenaMine,4,4'-(9H-fluoren-9-ylidene)bis- 4,4'-9-Fluorenylidene)dianilane 9,9-Bis(4-aMinophenyl)fluorene (BAFL) AKOS BBB/416 9,9'-BIS (4-AMINOPHENYL) FLUORENE 9,9-BIS(4-AMINOPHENYL)FLUORENE 4,4'-(9-FLUORENYLIDENE)DIANILINE 4,4'-(9-Fluorenylidene)dianiline 99% 9,9-Bis(4-aminophenyl)fluorene(FDA) BIO-FARMA BF003152 TIMTEC-BB SBB008629 Bis(4-aminophenyl)fluorene 9,9-Bis(4-aminophenyl)-9H-fluorene 9H-Fluorene-9,9-diylbis(p-phenylene)diamine Anilinefluorene bisaminophenylfluorene 9,9-Bis(4-aminophenyl)fluorene (refined product of B1549) Zinc03897005 9,9-Bis(4-aminophenyl)fluorene (purified by sublimation) 2-[9-(2-aMinophenyl)-9H-fluoren-9-yl]aniline 9,9-bis(aminophenyl)fluorene 4,4'-(9H-fluorene-9,9-diyl)dianiline 4,4''-(9-FLUOROENYLIDENE)DIANILINE 9-[Bis-(4-anilino)]-fluorene 9,9-BIS(4-AMINOPHENYL)FLUORENE ---POWDER, 99%--- 4,4'-(9H-Fluoren-9-ylidene)bisaniline 4,4'-(9H-Fluorene-9,9-diyl)bis(aniline) 4,4'-(9H-Fluorene-9-ylidene)dianiline 4-[9-(4-aminophenyl)fluoren-9-yl]aniline 9,9-Bis(4-aminophenyl)fluorene 15499-84-0 4,4'-(9-Fluorenylidene)dianiline 15499-84-0 9,9-Bis(4-aminophenyl)fluorene (purified by sublimation)> 9,9-Bis(4-aminophenyl)fluorene > 9,9-bis(4-aminopheny|) fluorene FDA BAFL 9,9-Bis(4-aminophenyl)fluorene (BAPF) 9,9-BIS(4-AMINOPHENYL)FLUORENE(BAF) 9,9-bis(4-aminopheny 4,4'-(9H-Fluorene-9,9-diyl)dianiline 4,4'-(9-Fluorenylidene)dianiline 15499-84-0 C25H20N2 Nitrogen Compounds Organic Building Blocks Polyamines Building Blocks Reagent for High-Performance Polymer Research Fluorenes & Fluorenones Fluorenes, etc. (reagent for high-performance polymer research) Fluorenes Electroluminescence Electronic Chemicals Electroluminescence Fluorenes Fluorenes & Fluorenones Fluorenes, etc. (reagent for high-performance polymer research) Functional Materials