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2-Hydroxy-1-propyl Methanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 113391-95-0 Structure
  • Basic information

    1. Product Name: 2-Hydroxy-1-propyl Methanesulfonate
    2. Synonyms: 2-Hydroxy-1-propyl Methanesulfonate
    3. CAS NO:113391-95-0
    4. Molecular Formula: C4H10O4S
    5. Molecular Weight: 154.1848
    6. EINECS: N/A
    7. Product Categories: Aliphatics;Sulfur & Selenium Compounds;Aliphatics, Sulfur & Selenium Compounds
    8. Mol File: 113391-95-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Hydroxy-1-propyl Methanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Hydroxy-1-propyl Methanesulfonate(113391-95-0)
    11. EPA Substance Registry System: 2-Hydroxy-1-propyl Methanesulfonate(113391-95-0)
  • 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: 113391-95-0(Hazardous Substances Data)

113391-95-0 Usage

Uses

2-Hydroxy-1-propyl Methanesulfonate is used in the preparation of labeled cocaine analogs.

Check Digit Verification of cas no

The CAS Registry Mumber 113391-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,9 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113391-95:
(8*1)+(7*1)+(6*3)+(5*3)+(4*9)+(3*1)+(2*9)+(1*5)=110
110 % 10 = 0
So 113391-95-0 is a valid CAS Registry Number.

113391-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Hydroxy-1-propyl Methanesulfonate

1.2 Other means of identification

Product number -
Other names 2-hydroxypropyl methanesulfonate

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:113391-95-0 SDS

113391-95-0Downstream Products

113391-95-0Relevant articles and documents

NUCLEOPHILIC CHARACTERISTICS OF NUCLEOFUGIC ANIONS IN THE CLEAVAGE OF EPOXIDES BY PROTIC ACIDS AND NITRONIUM FLUOROBORATE

Zefirov, N. S.,Kirin, V. N.,Yur'eva, N. M.,Zhdankin, V. V.,Kozmin, A. S.

, p. 1264 - 1279 (2007/10/02)

The cleavage of ethylene, propylene, and cyclohexene oxides by protic acids RCOOH (R= CH3, CF3) in the presence of sources of nucleophilic anions (the lithium or tetrabutylammonium salts of perchloric or substituted sulfonic acids) leads to the formation not only of 2-hydroxyalkyl carboxylates but also of significant amounts of 2-hydroxyalkyl perchlorates and sulfonates.In the reactions of the same oxides with nitronium fluoroborate and the above-mentioned salts in methylene chloride 2-perchloryl- and 2-sulfonyloxyalkyl nitrates are formed with high yields; these are the products from opening of the epoxide ring and subsequent combination of the perchlorate and substituted sulfonate ions.The investigated processes extend the range of reactions involving the concurrent combination of nucleofugic anions and can be used as a method for the production of β-hydroxy- and β-nitroxyalkyl perchlorates and sulfonates.

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