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9-Fluorenone

9-Fluorenone Structure
CAS No.
486-25-9
Chemical Name:
9-Fluorenone
Synonyms
9H-FLUOREN-9-ONE;FLUORENONE;FLUOREN-9-ONE;9H-fluorene-9-one;uorenone;9-FLUORENON;9-FLUORENONE;Dluoren-9-one;9-Fluoreneone;9-oxofluorene
CBNumber:
CB2304953
Molecular Formula:
C13H8O
Molecular Weight:
180.2
MOL File:
486-25-9.mol
MSDS File:
SDS
Modify Date:
2024/7/29 15:17:36

9-Fluorenone Properties

Melting point 80-83 °C (lit.)
Boiling point 342 °C (lit.)
Density 0,9 g/cm3
vapor pressure 0.005-0.2Pa at 20-50℃
refractive index 1.6309 (estimate)
Flash point 163 °C
storage temp. Store below +30°C.
solubility DMSO (Slightly), Methanol (Slightly)
form Crystalline Powder or Flakes
color Yellow
Water Solubility insoluble
BRN 1636531
Stability Stable. Combustible. Incompatible with strong oxidizing agents.
InChIKey YLQWCDOCJODRMT-UHFFFAOYSA-N
LogP 3.25 at 25℃ and pH7.7
CAS DataBase Reference 486-25-9(CAS DataBase Reference)
NIST Chemistry Reference 9H-Fluoren-9-one(486-25-9)
EPA Substance Registry System 9-Fluorenone (486-25-9)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07,GHS09
Signal word  Warning
Hazard statements  H319-H411
Precautionary statements  P273-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  24/25-36/37/39-27-26
WGK Germany  3
RTECS  LL8925000
Autoignition Temperature 608 °C
Hazard Note  Irritant
TSCA  Yes
HS Code  29143900
Toxicity LD50 orally in Rabbit: > 3900 mg/kg
NFPA 704
1
1 0

9-Fluorenone price More Price(14)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) F1506 9-Fluorenone 98% 486-25-9 5G ₹2294.9 2022-06-14 Buy
Sigma-Aldrich(India) F1506 9-Fluorenone 98% 486-25-9 100G ₹2976.88 2022-06-14 Buy
Sigma-Aldrich(India) F1506 9-Fluorenone 98% 486-25-9 500G ₹10348.7 2022-06-14 Buy
Sigma-Aldrich(India) 8.03977 9-Fluorenone for synthesis 486-25-9 250G ₹10989.99 2022-06-14 Buy
ALFA India ALF-A12910-36 9-Fluorenone, 98+% 486-25-9 500g ₹6987 2022-05-26 Buy
Product number Packaging Price Buy
F1506 5G ₹2294.9 Buy
F1506 100G ₹2976.88 Buy
F1506 500G ₹10348.7 Buy
8.03977 250G ₹10989.99 Buy
ALF-A12910-36 500g ₹6987 Buy

9-Fluorenone Chemical Properties,Uses,Production

Description

9-fluorenone is an important intermediate for organic synthesis. It can be used to manufacture a variety of fine chemicals, mainly used as a modifier for the production of polymer materials, bisphenol fluorene, fluorenyl benzoxazine resin, acrylic resin, polyester, polycarbonate and epoxy resin. In the laboratory, fluorene was used as the raw material, dimethyl sulfoxide as the solvent, sodium hydroxide as the catalyst and oxygen as the oxidant. The oxidizing reaction was carried out by a tower packing reactor. The reaction solution was cooled and filtered to obtain a crude fluorenone. The content of crude fluorenone is 93%. We can recover 94% of the solvent and part of the crude fluorenone through distillation of the filtrate. The crude fluorenone is purified by directional crystallization to obtain yellow flaky fluorenone that have a purity of 99.8% or more.

Chemical Properties

yellow flakes, chips or crystalline powder; Soluble in ethanol and ether, insoluble in water.

Uses

9-Fluorenone is used in the preparation of antimalarial drugs. It is a fluorene derivative. Further, it is used in functional polymer and in dyes.

Application

9-Fluorenone has been extensively used as a precursor to synthesize a variety of organic electronic materials. Some of the general examples are:
Synthesis of host for the blue and green phosphorescent organic light emitting diodes (PHOLEDs).
Synthesis of fluorene-based molecular motors.
Synthesis of open-shell Chichibabin′s hydrocarbons as potential organic spintronic materials.
It also acts as a sensitizer in the formation of picene via photosensitization of 1,2-di(1-naphthyl)ethane.

Definition

ChEBI: Fluoren-9-one is the simplest member of the class fluoren-9-ones that is 9H-fluorene bearing an oxo substituent at position 9. It has a role as a fungal xenobiotic metabolite.

Preparation

Fluorenone can be produced by catalytic oxidation of fluorene, or of fluorene fractions in the presence of a quarternary ammonium salt, or by catalytic oxidative cracking (oxicracking) of a suitable aromatic.

Purification Methods

Crystallise 9-fluorenone from absolute EtOH, MeOH or *benzene/pentane. [Ikezawa J Am Chem Soc 108 1589 1986.] Also recrystallise it twice from toluene and sublime it in a vacuum [Saltiel J Am Chem Soc 108 2674 1986]. It can be distilled under high vacuum. [Beilstein 7 H 465, 7 III 2330, 7 IV 1629.]

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9-FLUORENON 9-FLUORENONE FLUORENONE(9-) AURORA KA-7498 9-Fluorenone/9H-Fluoren-9-one 9-Fluorenone, 99+% 100GR Dluoren-9-one 9-FLUORENONE FOR SYNTHESIS 250 G 9H-Fluoren-9-one 98% 9-Oxo-9H-fluorene 9-Fluorenone 0 9-Fluoreneone 9-FLUORENONE PESTANAL, 250 MG 9-Fluorenone99% 9-Fluorenone,98% 9-oxofluorene Diphenyleneketone Fluoren-9-one 98% 9-oxofluorine fluorene ketone 9-FLUOROENONE 9-FLUORENONE, 98%9-FLUORENONE, 98%9-FLUORENONE, 98% F**9-Fluorenone uorenone JACS-486-25-9 9-Fluorenone> 9-Fluorenone (Stellar-2010) 9H-FLUOREN-9-ONE FLUORENONE FLUOREN-9-ONE 9H-fluorene-9-one 9-Fluoro none Tilorone Impurity 7 486-25-9 Fluorenes & Fluorenones Photopolymerization Initiators Fluorenones C13 to C14 Carbonyl Compounds Building Blocks Organic Building Blocks Ketones Fluorene Derivatives Fluorenes, Flurenones Fluorenes & Fluorenones Pharmaceutical intermediates Imidazoles ,Homopiperidines OLED materials,pharm chemical,electronic Fluorenones Functional Materials Photopolymerization Initiators Fused Ring Systems C13 to C14 Carbonyl Compounds Ketones bc0001