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126-63-6

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126-63-6 Usage

Description

BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is a colorless liquid with a mold odor, which is insoluble in water but miscible with most common organic solvents. It is a combustible compound known for its various applications across different industries due to its unique chemical properties.

Uses

Used in Heavy Metal Extraction:
BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is used as an extraction agent for the removal of heavy metals from various solutions, thanks to its ability to form complexes with metal ions.
Used in Solvent Separation:
In the solvent separation industry, BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is used as a separating agent to facilitate the separation of different solvents based on their solubility and miscibility properties.
Used in Gasoline Additive:
BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is used as an additive in the gasoline industry to enhance the performance and efficiency of the fuel, as well as to improve its combustion properties.
Used as an Antifoam Agent:
In various industrial processes, BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is used as an antifoam agent to prevent the formation of foam, which can interfere with the efficiency of the process.
Used as a Plasticizer:
In the plastics industry, BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is used as a plasticizer to increase the flexibility and workability of plastic materials.
Used as a Stabilizer:
BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is used as a stabilizer in various applications to prevent the degradation or breakdown of materials, ensuring their longevity and performance.
Used in Textile Conditioning:
In the textile industry, BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is used as a conditioner to improve the softness,手感 (hand feel), and overall quality of fabrics.
Used as an Antistatic Agent:
BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE is used as an antistatic agent in various applications to reduce the buildup of static electricity, which can cause issues in sensitive electronic equipment or during the manufacturing process.

Check Digit Verification of cas no

The CAS Registry Mumber 126-63-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126-63:
(5*1)+(4*2)+(3*6)+(2*6)+(1*3)=46
46 % 10 = 6
So 126-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C24H51O3P/c1-7-13-16-22(10-4)19-26-28(25,21-24(12-6)18-15-9-3)27-20-23(11-5)17-14-8-2/h22-24H,7-21H2,1-6H3

126-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name BIS(2-ETHYLHEXYL)-2-ETHYLHEXYLPHOSPHONATE

1.2 Other means of identification

Product number -
Other names O,O-bis(2-ethylhexyl) (2-ethylhexyl) phosphonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:126-63-6 SDS

126-63-6Downstream Products

126-63-6Relevant articles and documents

Selective Substitution of POCl 3 with Organometallic Reagents: Synthesis of Phosphinates and Phosphonates

Verbelen, Bram,Dehaen, Wim,Binnemans, Koen

, p. 2019 - 2026 (2018/04/14)

The selectivity of the substitution reaction of phosphoryl chloride with organometallic reagents was investigated using NMR spectroscopy. This led to the discovery that the selectivity of the substitution reaction can be tuned by choosing a proper organometallic reagent. A phosphinate could be obtained by using a Grignard reagent whereas an organozinc reagent provided a phosphonate. Based on these results, one-pot synthetic methods for the preparation of phosphinates and phosphonates using commercially available starting materials were developed. Both methods allow the synthesis of a broad range of either phosphinate or phosphonate derivatives in a straightforward and general procedure. Moreover, using these one-pot procedures, mixed systems substituted with different alkyl/aryl groups can be prepared.

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