Welcome to LookChem.com Sign In|Join Free

CAS

  • or

5927-50-4

Post Buying Request

5927-50-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5927-50-4 Usage

Description

Tetramethyl ethylenediphosphonate, a phosphorus-containing compound with the molecular formula C6H18O6P4, is a versatile chemical used in various industrial applications due to its flame retardant and chelating properties.

Uses

Used in Textile Industry:
Tetramethyl ethylenediphosphonate is used as a flame retardant for enhancing the fire resistance of textiles, ensuring safety and compliance with fire safety standards.
Used in Plastics Industry:
In the plastics industry, tetramethyl ethylenediphosphonate is used as a flame retardant to improve the fire safety of plastic products, reducing the risk of fire-related accidents.
Used in Rubber Industry:
Tetramethyl ethylenediphosphonate is used as a flame retardant in the production of rubber products, providing enhanced fire resistance and safety.
Used in Water Treatment:
Tetramethyl ethylenediphosphonate is used as a sequestering agent in water treatment processes, helping to remove impurities and improve water quality.
Used as a Scale Inhibitor:
In various industrial processes, tetramethyl ethylenediphosphonate is used as a scale inhibitor to prevent the formation of scale deposits, ensuring efficient operation and reducing maintenance costs.
Used in Pharmaceutical Production:
Due to its ability to form stable complexes with metal ions, tetramethyl ethylenediphosphonate is used in the production of pharmaceuticals, contributing to the development of effective drug formulations.
Used in Detergent Production:
Tetramethyl ethylenediphosphonate is used in the production of detergents, where it acts as a chelating agent to improve cleaning performance and prevent the formation of soap scum.
It is important to handle tetramethyl ethylenediphosphonate with care and store it properly, as it can be toxic if ingested or inhaled and can cause irritation to the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 5927-50-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5927-50:
(6*5)+(5*9)+(4*2)+(3*7)+(2*5)+(1*0)=114
114 % 10 = 4
So 5927-50-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H16O6P2/c1-9-13(7,10-2)5-6-14(8,11-3)12-4/h5-6H2,1-4H3

5927-50-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(dimethoxyphosphoryl)ethane

1.2 Other means of identification

Product number -
Other names Ethan-1,2-bis-phosphonsaeure-tetramethylester

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:5927-50-4 SDS

5927-50-4Downstream Products

5927-50-4Relevant articles and documents

A salt-free synthesis of 1,2-bisphosphorylethanes via an efficient PMe3-catalyzed addition of >P(O)H to vinylphosphoryl compounds

Saga, Yuta,Han, Daoqing,Kawaguchi, Shin-Ichi,Ogawa, Akiya,Han, Li-Biao

supporting information, p. 5303 - 5305 (2015/08/26)

Abstract A convenient and versatile method was developed for the preparation of 1,2-bisphosphorylethanes. Thus, in the presence of a catalytic amount of trimethylphosphine, a variety of >P(O)H compounds efficiently add to vinylphosphoryl compounds to produce the corresponding 1,2-bisphosphorylethanes in high yields. In most cases, the trimethylphosphine catalyst was simply removed under vacuum leaving spectroscopically pure adducts. The present method provided a halogen and metal-free clean process for the preparation of 1,2-bisphosphorylethanes.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 5927-50-4