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Triethyl Phosphite (122-52-1)
Triethyl Phosphite (122-52-1)
Triethyl Phosphite (122-52-1)
Triethyl Phosphite (122-52-1)
Triethyl Phosphite (122-52-1)
Triethyl Phosphite (122-52-1)
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Triethyl Phosphite (122-52-1)

Price 2000.0 INR/ Kilograms

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MOQ : 25 Kilograms

Triethyl Phosphite (122-52-1) Specification

  • Physical Form
  • Liquid
  • Melting Point
  • -60 C
  • Application
  • Industrial
  • Appearance
  • Colorless to pale yellow liquid
  • Properties
  • Triethyl phosphite is a versatile organophosphorus reagent widely used in the Michaelis-Arbuzov reaction to synthesize phosphonate esters. These products are crucial intermediates in the production of flame retardants, plasticizers, and complex pharmaceuticals. It also serves as a potent reducing agent for various organic functional groups in synthesis.v
  • Usage
  • Phosphite ester reagent in organic synthesis; used as a phosphite donor in radical and condensation reactions; intermediate in synthesis of phosphorus-containing compounds
  • Molecular Weight
  • 166.16 g/mol Grams (g)
  • Molecular Formula
  • C6H15O3P
  • Purity
  • 98 99%
  • CAS No
  • 122-52-1
  • Structural Formula
  • C6H15O3P
  • Refractive Rate
  • 1.43
  • Solubility
  • Immiscible with water; soluble in organic solvents
 

Triethyl Phosphite (122-52-1) Trade Information

  • Minimum Order Quantity
  • 25 Kilograms
  • Payment Terms
  • Cash in Advance (CID)
  • Supply Ability
  • 5000 Kilograms Per Month
  • Delivery Time
  • 10 Days
  • Main Domestic Market
  • All India
 

About Triethyl Phosphite (122-52-1)

We are Supplier, Exporter and Contract Manufacturer.
Technical profile of Triethyl Phosphite, a high-purity raw chemical material supplied by Triveni Chemicals for industrial manufacturing and laboratory synthesis.

Technical Specifications:
CAS Number: 122-52-1
Synonyms: Phosphorous Acid Triethyl Ester
Chemical Formula: C6H15O3P

Industrial Uses & Applications:
It Is Widely Used As An Intermediate And Reagent In Organic Synthesis, Particularly In The Manufacture Of Phosphonates, Pharmaceuticals, Agrochemicals, And Plastic Additives. It Is An Organophosphorus Compound That Readily Undergoes Oxidation And Esterification Reactions.


Versatile Organophosphorus Reagent

Triethyl phosphite is essential in organic chemistry, primarily enabling the Michaelis-Arbuzov reaction to produce phosphonate esters. Its versatility extends to serving as a reducing agent for transforming diverse organic functional groups, broadening its utility in industrial and research settings.


Key Applications in Industry

This compound is integral to the manufacturing of flame retardants, plasticizers, and complex pharmaceuticals. Its specialized properties support the efficient production of phosphorus-containing intermediates, contributing to advancements in material safety and pharmaceutical innovation.

FAQ's of Triethyl Phosphite (122-52-1):


Q: How is triethyl phosphite commonly used in industrial applications?

A: Triethyl phosphite is extensively used as a phosphite ester reagent in organic synthesis, especially for the Michaelis-Arbuzov reaction, leading to the creation of phosphonate esters. These are crucial intermediates in the production of flame retardants, plasticizers, and some pharmaceuticals.

Q: What are the main benefits of using triethyl phosphite in synthesis?

A: The main advantage of triethyl phosphite is its effectiveness as a reducing agent and its capacity to introduce phosphorus into organic molecules, facilitating the synthesis of valuable intermediates while enhancing process efficiency and reliability.

Q: When should triethyl phosphite be applied in organic synthesis?

A: Triethyl phosphite is typically used when phosphorus-containing groups are to be introduced into a molecule, or when a potent reducing agent is required for modifying various organic functional groups during synthesis.

Q: Where is triethyl phosphite commonly manufactured and supplied?

A: Triethyl phosphite is produced and supplied globally, with several reputable manufacturers and suppliers based in India catering to the industrial and research needs for this reagent.

Q: What is the process of using triethyl phosphite in the Michaelis-Arbuzov reaction?

A: In the Michaelis-Arbuzov reaction, triethyl phosphite reacts with alkyl halides to generate phosphonate esters. The process involves heating the reagents together, promoting the transfer of an ethoxy group to form the desired phosphorus-carbon bond.

Q: Is triethyl phosphite soluble in water?

A: No, triethyl phosphite is immiscible with water but is soluble in many organic solvents, making it appropriate for a variety of organic synthesis applications where water-free conditions are necessary.

Q: What safety precautions are important when handling triethyl phosphite?

A: While using triethyl phosphite, it is essential to operate in a well-ventilated area and wear suitable protective equipment, as it is a chemical reagent that should be handled with care to avoid exposure and potential reactions with moisture.

Triethyl Phosphite (122-52-1)
Triethyl Phosphite (122-52-1)
Triethyl Phosphite (122-52-1)
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