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5008-73-1

ISOPROPYL N-PROPYL SULFIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 5008-73-1 Structure

  • Basic information

    1. Product Name: ISOPROPYL N-PROPYL SULFIDE
    2. Synonyms: 1-(Isopropylsulfanyl)propane;2-methyl-3-thiahexane;Isopropylpropyl sulfide;isopropylpropylsulfide;n-Propyl isopropyl sulfide;propane,1-[(1-methylethyl)thio]-;Propyl isopropyl sulfide;propylisopropylsulfide
    3. CAS NO:5008-73-1
    4. Molecular Formula: C6H14S
    5. Molecular Weight: 118.24
    6. EINECS: 225-686-0
    7. Product Categories: N/A
    8. Mol File: 5008-73-1.mol

  • Chemical Properties

    1. Melting Point: -96.69°C (estimate)
    2. Boiling Point: 132 °C
    3. Flash Point: 23°C
    4. Appearance: /liquid (estimate)
    5. Density: 0.83
    6. Vapor Pressure: 10.1mmHg at 25°C
    7. Refractive Index: 1.4430 to 1.4460
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ISOPROPYL N-PROPYL SULFIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: ISOPROPYL N-PROPYL SULFIDE(5008-73-1)
    12. EPA Substance Registry System: ISOPROPYL N-PROPYL SULFIDE(5008-73-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: R10:Flammable.;
    3. Safety Statements: S23:Do not inhale gas/fumes/vapour/spray.; S24/25:Avoid contact with skin and eyes.;
    4. RIDADR: UN 1993 3/PG III
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 3
    8. PackingGroup: III
    9. Hazardous Substances Data: 5008-73-1(Hazardous Substances Data)

5008-73-1 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 3627, 1951 DOI: 10.1021/ja01152a021

Check Digit Verification of cas no

The CAS Registry Mumber 5008-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5008-73:
(6*5)+(5*0)+(4*0)+(3*8)+(2*7)+(1*3)=71
71 % 10 = 1
So 5008-73-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H14S/c1-4-5-7-6(2)3/h6H,4-5H2,1-3H3

5008-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Isopropyl Propyl Sulfide

1.2 Other means of identification

Product number -
Other names Propane, 1-[(1-methylethyl)thio]-

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:5008-73-1 SDS

5008-73-1Relevant articles and documents

Alkyl- and Arylsulfenanilides by Cycloelimination of Propene from N-Aryl-S-isopropyl-sulfimides

Claus, Peter K.,Silbernagel, Waltraud,Franek, Walter,Rieder, Werner

, p. 841 - 850 (2007/10/02)

A series of N-aryl-S-isopropyl-S-alkyl- or aryl-sulfimides has been prepared and transformed into alkyl- or arylsulfenanilides, respectively, by thermal cycloelimination of propene. - Keywords: Sulfimides; Sulfenanilides; Thermolysis; Cycloelimination.

Reactivity of Chalcogen Cluster Polycations

Rosan, A. M.

, p. 377 - 378 (2007/10/02)

The chalcogen polycations S8(AsF6)2, S19(HS2O7)2, and Se4(HS2O7)2 are powerful oxidants entering into electron transfer reactions with hydrocarbons, aromatic compounds, and halides.

EFFET PROMOTEUR DES PHOSPHITES ALIPHATIQUES DANS L'ADDITION PHOTO AMORCEE D'H2S SUR LE PROPYLENE EN SOLUTION. I - ETUDE ANALYTIQUE

Brehon, Annick,Couture, Axel,Combier, Lablache A.

, p. 839 - 850 (2007/10/02)

Aliphatic phosphites have a promotor effect in the radical addition in solution of H2S to propylene photoinitiated as well by direct H2S irradiation as by added benzophenone irradiation.For this last reaction, the phosphite used being (CH3O)3P, the solvent polarity has no effect on the reaction.When the solvent used is a poor hydrogen donnor in a radical reaction, such as benzene, there is an induction period in the case of the benzophenone photoinitiated reaction performed in the presence of a phosphite.It increases for a given aliphatic phosphite with the phosphite concentration and varies with the aliphatic phosphites structure.Light intensity has nearly no effect on the development of the last reaction.

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