ChemicalBook > CAS DataBase List > Anthracen-9-ol

Anthracen-9-ol

Product Name
Anthracen-9-ol
CAS No.
529-86-2
Chemical Name
Anthracen-9-ol
Synonyms
9-Anthracenol;Anthracen-9-ol;Anthracen-9-ol DISCONTINUED PLEASE SEE A679600
CBNumber
CB2967789
Molecular Formula
C14H10O
Formula Weight
194.23
MOL File
529-86-2.mol
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Anthracen-9-ol Property

Melting point:
120° (if bath is heated to 110°); mp 152° (if bath is cold at start)
Boiling point:
290.68°C (rough estimate)
Density 
1.0550 (rough estimate)
refractive index 
1.5500 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
9.40±0.30(Predicted)
Water Solubility 
35.93mg/L(25 ºC)
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
CHM0310577
Product name
9-HYDROXYANTHRACENE
Purity
95.00%
Packaging
5MG
Price
$500.21
Updated
2021/12/16
Aaron Chemicals
Product number
AR00DHUS
Product name
Anthracen-9-ol
Purity
95%
Packaging
1g
Price
$604
Updated
2021/12/16
Aaron Chemicals
Product number
AR00DHUS
Product name
Anthracen-9-ol
Purity
95%
Packaging
250mg
Price
$188
Updated
2021/12/16
Alichem
Product number
529862
Product name
Anthracen-9-ol
Packaging
100g
Price
$400
Updated
2021/12/16
Abosyn
Product number
61-11020
Product name
Anthracen-9-ol
Purity
95-98%
Packaging
1g
Price
$432
Updated
2021/12/16
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Anthracen-9-ol Chemical Properties,Usage,Production

Chemical Properties

Crystals. Soluble in organic solvents with a blue fluorescence. Changes in solution to anthrone. Combustible.

Uses

Dyes.

Definition

ChEBI: 9-anthrol is an anthrol. It is a tautomer of an anthrone.

Synthesis

642-31-9

529-86-2

The general procedure for the synthesis of 9-hydroxyanthracene from 9-anthracenecarboxaldehyde is as follows: in a 1,000 mL round-bottomed flask equipped with a stirrer and thermometer, 20.00 g of 9-formylanthracene and 200 mL of acetic acid were added. After stirring the reaction mixture for 15 minutes, 45.68 g of sodium percarbonate was slowly added at room temperature. Subsequently, the reaction temperature was raised to 30 °C and the reaction mixture was continuously stirred, and the progress of the reaction was monitored by thin-layer chromatography (TLC; unfolding agent: n-hexane/ethyl acetate, 4:1). Upon completion of the reaction, the acetic acid was removed by distillation under reduced pressure and the reaction mixture was concentrated. To the concentrate, 200 mL of toluene was added and the toluene layer was washed sequentially with 100 mL of water, 100 mL of 10% sodium thiosulfate solution and 100 mL of 10% sodium hydroxide solution. Next, 22.75 g of methanol and 0.65 g of sulfuric acid were added to the toluene layer, and the resulting methyl formate and methanol were removed by distillation at atmospheric pressure. Then, 82.47 g of 10% sodium hydroxide solution was added to the toluene layer, and after stirring at room temperature, the toluene layer and the basic aqueous solution layer were separated using a partition funnel. The basic aqueous solution layer was washed several times with 20 mL of dichloromethane to remove small amounts of residual impurities (e.g., anthracene, 9-formylanthracene, etc.) until the aqueous layer was free of impurities by TLC. Subsequently, the basic aqueous solution layer was adjusted to a slightly acidic pH with concentrated sulfuric acid. the slightly reddish powder obtained was filtered and recrystallized in toluene to obtain pure 9-hydroxyanthracene (yield: 78%, purity: 99.56%).

References

[1] Patent: KR101661742, 2016, B1. Location in patent: Paragraph 0084; 0085

Anthracen-9-ol Preparation Products And Raw materials

Raw materials

Preparation Products

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Anthracen-9-ol Suppliers

Finetech Industry Limited
Tel
027-87465837 19945049750
Fax
027-8777-2287
Email
sales@finetechnology-ind.com
Country
China
ProdList
9637
Advantage
58
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15873
Advantage
55
Henan CoreyChem Co., Ltd
Tel
0371-86658258
Fax
0371-60996044
Email
info@coreychem.com
Country
China
ProdList
10453
Advantage
58
BePharm Ltd
Tel
400-685-9117
Fax
021-51816740
Email
market@bepharm.com
Country
China
ProdList
15081
Advantage
60
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Zhengzhou JACS Chemical Co., Ltd.
Tel
0371-0371-86259281 15981966935
Fax
0371-86259281
Email
jacschem@163.com
Country
China
ProdList
2005
Advantage
58
Henan's chemical products co., LTD
Tel
0371-60919097 15378766539
Fax
0371-60919097
Email
794449696@qq.com
Country
China
ProdList
4996
Advantage
58
Jiangsu aikang biomedical research and development co., LTD
Tel
025-58859352 13155353615
Email
qzhang@aikonchem.com
Country
China
ProdList
15525
Advantage
58
Henan Alfa Chemical Co., Ltd
Tel
+8615838112936
Email
alfa10@alfachem.cn
Country
China
ProdList
12921
Advantage
58
Finetech Industry Limited
Tel
+86-27-8746-5837 +8619945049750
Fax
86 27 87772287
Email
info@finetechnology-ind.com
Country
China
ProdList
9629
Advantage
58
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View Lastest Price from Anthracen-9-ol manufacturers

Career Henan Chemical Co
Product
Anthracen-9-ol 529-86-2
Price
US $9.80/KG
Min. Order
1g
Purity
≥99%
Supply Ability
100kg
Release date
2019-12-21

529-86-2, Anthracen-9-olRelated Search:


  • Anthracen-9-ol
  • 9-Anthracenol
  • Anthracen-9-ol DISCONTINUED PLEASE SEE A679600
  • 529-86-2