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CAS

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29379-41-7

1-Propoxyoctane, also known as octane-1-propyl ether, is an organic compound with the chemical formula C11H24O. It is a colorless, flammable liquid that is insoluble in water but soluble in organic solvents. This ether derivative is formed by the reaction of 1-propanol and octyl bromide, and it is commonly used as a solvent, a chemical intermediate, and in the synthesis of various compounds. Due to its potential health and environmental risks, it is important to handle 1-propoxyoctane with care, following proper safety guidelines.

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  • 29379-41-7 Structure

  • Basic information

    1. Product Name: 1-propoxyoctane
    2. Synonyms: 1-Propoxyoctane; Ether, octyl propyl; octane, 1-propoxy-; Octyl propyl ether
    3. CAS NO:29379-41-7
    4. Molecular Formula: C11H24O
    5. Molecular Weight: 172.3077
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29379-41-7.mol

  • Chemical Properties

    1. Melting Point: -46.0 °C
    2. Boiling Point: 207.3°C at 760 mmHg
    3. Flash Point: 68.5°C
    4. Appearance: N/A
    5. Density: 0.795g/cm3
    6. Vapor Pressure: 0.327mmHg at 25°C
    7. Refractive Index: 1.419
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-propoxyoctane(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-propoxyoctane(29379-41-7)
    12. EPA Substance Registry System: 1-propoxyoctane(29379-41-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 29379-41-7(Hazardous Substances Data)

29379-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29379-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,7 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29379-41:
(7*2)+(6*9)+(5*3)+(4*7)+(3*9)+(2*4)+(1*1)=147
147 % 10 = 7
So 29379-41-7 is a valid CAS Registry Number.

29379-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-propoxyoctane

1.2 Other means of identification

Product number -
Other names 1-propoxy-octane

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:29379-41-7 SDS

29379-41-7Downstream Products

29379-41-7Relevant articles and documents

Continuous-Flow Reductive Alkylation: Synthesis of Bio-based Symmetrical and Disymmetrical Ethers

Bruniaux, Sophie,Luart, Denis,Len, Christophe

, p. 1849 - 1856 (2018/02/06)

For the first time, a reductive alkylation process in continuous flow has been elaborated for the conversion of bio-based alcohols and aldehydes into symmetrical and dissymmetrical high-value-added ethers for industrial companies. The developed method is an etherification associating liquid, solid and gas phases under green conditions (continuous flow, catalysis, bio-based starting materials).

Indium-catalyzed radical reductions of organic halides with hydrosilanes

Miura, Katsukiyo,Tomita, Mitsuru,Yamada, Yusuke,Hosomi, Akira

, p. 787 - 792 (2007/10/03)

(Equation Presented) The In(OAc)3-catalyzed reaction of bromo- and iodoalkanes with PhSiH3 in THF at 70°C gave dehalogenated alkanes in good to high yields. In the presence of Et3B and air, the reduction proceeded smoothly at 30°C. When 2,6-lutidine and air were used as additives, the In(OAc)3-catalyzed system enabled an efficient reduction of simple and functionalized iodoalkanes in EtOH. Catalytic use of GaCl3 was found to be effective in the reduction of haloalkanes with poly(methylhydrosiloxane) (PMHS). These catalytic reductions probably involve a radical chain mechanism in which indium or gallium hydride species work as the actual reductants.

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