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1-ACENAPHTHENOL

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1-ACENAPHTHENOL Basic information

Product Name:
1-ACENAPHTHENOL
Synonyms:
  • 1-Acenaphthenol (Acenaphthene-1-hydroxy)
  • 1-Acenaphthylenol, 1,2-dihydro- (9CI)
  • A406_ALDRICH
  • Acenaphthene-1-ol
  • EINECS 228-618-8
  • NSC 22834
  • NSC22834
  • 28807-94-5
CAS:
6306-07-6
MF:
C12H10O
MW:
170.21
EINECS:
228-618-8
Product Categories:
  • Aromatic Phenols
Mol File:
6306-07-6.mol
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1-ACENAPHTHENOL Chemical Properties

Melting point:
145-148 °C (lit.)
Boiling point:
369℃
Density 
1.290
Flash point:
129℃
storage temp. 
-20°C Freezer
solubility 
Chloroform (Slightly, Sonicated), Methanol (Slightly)
form 
Solid
pka
13.68±0.20(Predicted)
color 
Yellow to Dark Yellow
BRN 
2048222
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference
6306-07-6(CAS DataBase Reference)
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Safety Information

WGK Germany 
3
HS Code 
2906.29.6000
HazardClass 
IRRITANT

MSDS

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1-ACENAPHTHENOL Usage And Synthesis

Description

1-Acenaphthenol is a white to cream solid in appearance. It is almost insoluble in water. 1-Acenaphthenol is a stable and combustible chemical substance. It is incompatible with strong oxidising agents. It is used in the syntheses of organic compounds. Exposures to 1-acenaphthenol cause irritant effects. It is harmful by ingestion, inhalation, as well as through skin absorption. There are no complete data on the toxicology of 1-acenaphthenol.

Chemical Properties

1-Acenaphthenol is a white to cream solid in appearance. It is almost insoluble in water. 1-Acenaphthenol is a stable and combustible chemical substance. It is incompatible with strong oxidizing agents. It is used in the syntheses of organic compounds.

Uses

1-Acenaphthenol is a product of the microbial metabolism and photolysis of acenaphthene, of acenaphthene, a polycyclic hydrocarbon that has potential to act as polyploidizing agents in plants. 1-Acenaphthenol is also a known substrate of dihydrodiol dehydrogenases.

Health Hazard

Exposures to 1-acenaphthenol cause irritant effects. It is harmful by ingestion, inhalation, or skin absorption. There are no complete data on the toxicology of 1-acenaphthenol.

Purification Methods

If highly coloured (yellow), dissolve it in boiling *benzene (14g in 200mL), add charcoal (0.5g), filter it through a heated funnel, concentrate to 100mL and cool to give almost colourless needles. *Benzene vapour is TOXIC; use an efficient fume cupboard. The acetate has b 166-168o/5mm (bath temperature 180-185o). [Cason Org Synth Coll Vol III 3 1955.] It can also be recrystallised from *C6H6 or EtOH [Fieser & Cason J Am Chem Soc 62 432 1940]. It forms a brick-red crystalline complex with 2,4,5,7-tetranitrofluoren-9-one which is recrystallised from AcOH and is dried in a vacuum over KOH and P2O5 at room temperature, m 170-172o [Newman & Lutz J Am Chem Soc 78 2469 1956]. [Beilstein 6 IV 4623.]

1-ACENAPHTHENOL Preparation Products And Raw materials

Raw materials

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