Pyrene, 1,2,3,6,7,8-hexahydro- (8CI)(9CI)

Pyrene, 1,2,3,6,7,8-hexahydro- (8CI)(9CI) - Names and Identifiers

Name	1,2,3,6,7,8-Hexahydropyrene
Synonyms	NSC 60599 1,2,3,6,7,8-Hexahydropyrene 1,2,3,6,7,8-HEXAHYDROPYRENE pyrene,1,2,3,6,7,8-hexahydro- Pyrene, 1,2,3,6,7,8-hexahydro- (8CI)(9CI)
CAS	1732-13-4
EINECS	217-061-6
InChI	InChI=1/C16H16/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h7-10H,1-6H2

Pyrene, 1,2,3,6,7,8-hexahydro- (8CI)(9CI) - Physico-chemical Properties

Molecular Formula	C16H16
Molar Mass	208.3
Density	1.0102 (estimate)
Melting Point	130-134°C(lit.)
Boling Point	282.51°C (rough estimate)
Flash Point	213.3°C
Water Solubility	229.1ug/L(4 ºC)
Solubility	Chloroform (Slightly), DMSO (Slightly)
Vapor Presure	3.69E-06mmHg at 25°C
Appearance	Solid
Color	Off-White
Storage Condition	Refrigerator
Refractive Index	1.5000 (estimate)
MDL	MFCD00010584

Pyrene, 1,2,3,6,7,8-hexahydro- (8CI)(9CI) - Risk and Safety

Safety Description	S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes.
WGK Germany	3

Pyrene, 1,2,3,6,7,8-hexahydro- (8CI)(9CI) - Introduction

1,2,3,6,7,8-hexahydropyrene, also known as hexahydronaphthalene, is an organic compound. The following is an introduction to its nature, use, formulation and safety information:

Nature:
- 1,2,3,6,7,8-hexahydropyrene is a colorless to pale yellow solid.
-Its molecular formula is C10H12 and its molecular weight is 132.21g/mol.
-Hexahydropyrene is aromatic and has a typical naphthalene structure, but due to the addition of hydrogen atoms, it is more stable than pyrene.
-It has low solubility.

Use:
-Hexahydropyrene is mainly used as a starting material for organic synthesis. As an intermediate, it is widely used in the fields of pharmaceuticals, dyes and pesticides.
-It can also be used as a catalyst and reducing agent for hydrogenation reactions.
-Hexahydropyrene can be used as a light-emitting material for organic hybrid solar cells and organic light-emitting diodes.

Method:
-The preparation method of hexahydropyrene is usually obtained by the reduction reaction of hexahydronaphthalene. Typical reaction conditions are hydrogenation by reacting hexahydronaphthalene with hydrogen in the presence of hydrogen using a catalyst such as platinum, palladium or nickel.

Safety Information:
-Hexahydropyrene is less toxic to the human body under regular conditions, but it is still necessary to pay attention to proper laboratory operations.
-Since hexahydropyrene is an organic compound, prolonged exposure to high temperatures, fire sources and strong oxidants should be avoided.
-When handling hexahydropyrene, protective gloves and goggles must be worn to ensure good ventilation.
-Dispose of waste in accordance with local environmental regulations.

Last Update：2024-04-10 22:29:15