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1,4-Diiodo-2,5-dioctylbenzene, with the molecular formula C16H26I2, is an organic compound belonging to the alkylbenzene family. It is characterized by a benzene ring with two iodine atoms and two octyl groups attached to it. 1 4-DIIODO-2 5-DIOCTYLBENZENE is known for its stability and relative non-reactivity under normal conditions, which makes it suitable for various industrial and scientific applications.

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  • 171569-01-0 Structure
  • Basic information

    1. Product Name: 1 4-DIIODO-2 5-DIOCTYLBENZENE
    2. Synonyms: 1 4-DIIODO-2 5-DIOCTYLBENZENE
    3. CAS NO:171569-01-0
    4. Molecular Formula: C22H36I2
    5. Molecular Weight: 554.33018
    6. EINECS: N/A
    7. Product Categories: Aryl;C13 to C37+;Halogenated Hydrocarbons
    8. Mol File: 171569-01-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 502.2°C at 760 mmHg
    3. Flash Point: 228.5°C
    4. Appearance: /
    5. Density: 1.395g/cm3
    6. Vapor Pressure: 1.01E-09mmHg at 25°C
    7. Refractive Index: 1.551
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1 4-DIIODO-2 5-DIOCTYLBENZENE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1 4-DIIODO-2 5-DIOCTYLBENZENE(171569-01-0)
    12. EPA Substance Registry System: 1 4-DIIODO-2 5-DIOCTYLBENZENE(171569-01-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 22-24/25
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 171569-01-0(Hazardous Substances Data)

171569-01-0 Usage

Uses

Used in Chemical Synthesis:
1,4-Diiodo-2,5-dioctylbenzene is used as a reagent in the chemical synthesis of other organic compounds. Its unique structure allows it to participate in a variety of chemical reactions, contributing to the formation of new molecules with different properties and applications.
Used in Laboratory Research:
1 4-DIIODO-2 5-DIOCTYLBENZENE is also utilized in laboratory research, where it can be employed to study various chemical reactions and processes. Its stability and non-reactivity make it an ideal candidate for controlled experiments and the investigation of reaction mechanisms.
Used in the Production of Specialty Chemicals:
1,4-Diiodo-2,5-dioctylbenzene finds application in the production of specialty chemicals, which are tailored for specific industries and applications. Its unique properties and reactivity can be harnessed to create chemicals with desired characteristics, such as improved performance or enhanced stability.

Check Digit Verification of cas no

The CAS Registry Mumber 171569-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,5,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 171569-01:
(8*1)+(7*7)+(6*1)+(5*5)+(4*6)+(3*9)+(2*0)+(1*1)=140
140 % 10 = 0
So 171569-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H36I2/c1-3-5-7-9-11-13-15-19-17-22(24)20(18-21(19)23)16-14-12-10-8-6-4-2/h17-18H,3-16H2,1-2H3

171569-01-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Diiodo-2,5-dioctylbenzene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:171569-01-0 SDS

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