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Home > Encyclopedia > 2-Carboxyethyl(phenyl)phosphinic acid

2-Carboxyethyl(phenyl)phosphinic acid

2-Carboxyethyl(phenyl)phosphinic acid structure

2-Carboxyethyl(phenyl)phosphinic acid 

structure
  • CAS No:

    14657-64-8

  • Formula:

    C9H11O4P

  • Chemical Name:

    2-Carboxyethyl(phenyl)phosphinic acid

  • Synonyms:

    Propanoic acid,3-(hydroxyphenylphosphinyl)-;Propionic acid,3-(hydroxyphenylphosphinyl)-;3-(Hydroxyphenylphosphinyl)propanoic acid;2-Carboxyethyl(phenyl)phosphinic acid;3-(Phenylphosphinyl)propionic acid;3-(Hydroxyphenylphosphinyl)propionic acid;H 205 (flame retardant);H 205;Hiretar 205;2-Carboxylethyl(phenyl)phosphinic acid;Phosgard PF 100;PZ 1201

  • Categories:

    Inorganic Chemistry  >  Phosphorus Compounds

2-Carboxyethyl(phenyl)phosphinic acid Basic Attributes

214.15500

214.15

604-530-9

DTXSID30461246

2931900090

Characteristics

84.41000

-0.1

white powder

1.35 g/cm3

156-157 °C @ Solvent: Water

526.6ºC at 760 mmHg

272.3ºC

1.554

6.43E-12mmHg at 25°C

Safety Information

R41

26-39

Xi

P280, P305+P351+P338, P310

H318

|Danger|H318: Causes serious eye damage [Danger Serious eye damage/eye irritation]|P280, P305+P351+P338, and P310|H318 (100%): Causes serious eye damage [Danger Serious eye damage/eye irritation]|Aggregated GHS information provided by 19 companies from 1 notifications to the ECHA C&L Inventory.

2-Carboxyethyl(phenyl)phosphinic acid Use and Manufacturing

Methods of Manufacturing

A process for the production of 2-carboxyethylphenylphosphinic acid in accordance with the present invention without waste water, Next:(1) 1.0 mol of phenylphosphine dichloride was charged into a reaction vessel, stirred, heated to 80 ° C, 1 mol of acrylic acid was added dropwise, Finished warming to 110 deg C , heat 3 hours, cooling to 50 deg C ; (2) To the liquid obtained in the step (1), 2.0 mol of dichloropropane (secondary used mother liquor, Material complement), stirring;(3) to the step (2) to slowly drop 1.0mol of water, acid chloride intermediates and water hydrolysis reaction, drop finishedHeating to 90 DEG C, keeping for 3 hours, cooling to 20 DEG C to produce 2-carboxyethylphenylphosphinic acid, and recovering by-product hydrochloric acid.(4) The solid-liquid mixture obtained in step (3) was filtered, washed with dichloropropane, filtered again, placed in an oven, Baking at 130 ° C for 2 hours to obtain 2-carboxyethylphenylphosphinic acid, and the mother liquor was recovered in the next batch. The yield of 2-carboxyethylphenylphosphinic acid was 98.0percent, the melting point was 160.2 deg C , the acid value (mgKOH / g) was 522, the phosphorus content was 14.35percent, and the product quality was excellent.EXAMPLE 4 EXAMPLE 6

Uses

It is an important intermediate widely used in the preparation of organic phosphorus flame retardants, organic phosphorus pesticides, antioxidants, plasticizers, stabilizers, insecticides, catalysts and high-pressure lubricants, and paint molding agents.

Computed Properties

Molecular Weight:214.15
XLogP3:-0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:214.03949583
Monoisotopic Mass:214.03949583
Topological Polar Surface Area:74.6
Heavy Atom Count:14
Complexity:245
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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