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Bis(2-ethylhexyl) phosphate

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Bis(2-ethylhexyl) phosphate Basic information

Product Name:
Bis(2-ethylhexyl) phosphate
Synonyms:
  • PHOSPHORIC ACID BIS (2-ETHYLHEXYL) ESTER
  • PHOSPHORIC ACID DI(2-ETHYLHEXYL) ESTER
  • PHOSPHORIC ACID DIOCTYL ESTER
  • Phosphorsurebis-(2-ethylhexyl)-ester
  • isooctanol, hydrogen phosphate
  • DIETHYLHEXYL PHOSPHATE
  • Bis(2-ethylhexyl) Hydrogen Phosphate [for Rare Metals Extraction]
  • Dicapryl phosphate
CAS:
298-07-7
MF:
C16H35O4P
MW:
322.42
EINECS:
206-056-4
Product Categories:
  • Organics
  • Industrial/Fine Chemicals
  • organophosphorus compound
  • Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
  • Organic Phosphates/Phosphites
  • Phosphorus Compounds
  • orgainic intermediates
  • solvent
  • 298-07-7
  • K00001
  • bc0001
Mol File:
298-07-7.mol
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Bis(2-ethylhexyl) phosphate Chemical Properties

Melting point:
−60 °C(lit.)
Boiling point:
48 °C (12 mmHg)
Density 
0.965 g/mL at 25 °C(lit.)
vapor pressure 
<0.1 hPa (20 °C)
refractive index 
n20/D 1.443(lit.)
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
ethanol: soluble100mg/mL, clear
form 
Liquid
pka
1.47±0.50(Predicted)
Specific Gravity
0.974
color 
Colorless
PH
3 (< 1g/l, H2O)
Water Solubility 
slightly soluble
FreezingPoint 
-60℃
BRN 
1712988
Stability:
Moisture Sensitive
InChIKey
SEGLCEQVOFDUPX-UHFFFAOYSA-N
LogP
2.88 at 25℃
CAS DataBase Reference
298-07-7(CAS DataBase Reference)
NIST Chemistry Reference
Bis(2-ethylhexyl)hydrogen phosphate(298-07-7)
EPA Substance Registry System
Bis(2-ethylhexyl) phosphate (298-07-7)
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Safety Information

Hazard Codes 
C
Risk Statements 
21-34
Safety Statements 
26-36/37/39-45-25
RIDADR 
UN 1902 8/PG 3
WGK Germany 
1
RTECS 
TB7875000
Autoignition Temperature
255 °C
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29190090
Hazardous Substances Data
298-07-7(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 4940 mg/kg LD50 dermal Rabbit 1250 mg/kg

MSDS

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Bis(2-ethylhexyl) phosphate Usage And Synthesis

Chemical Properties

clear colorless to light yellow liquid

Uses

Additive to lubrication oils, corrosion inhibitor, and antioxidant. Used as extractant in the hydrometallurgical separation of cobalt and nickel. Metal extraction and separation, intermediate for wetting agents and detergents . Feedstock for chemical synthesis; extraction fluid for metal salts; cation extracting agent.

Uses

Extraction of metals.Bis(2-ethylhexyl) phosphate is used as a lubricant additive, corrosion inhibitor and a metal extractant. It is involved in the solvent extraction of uranium salts and rare earth metals. Iron(II) ions are extracted after reduction of Iron(III) ions. Further, it is used as a plasticizer and as a solvent in the synthesis of plastic.

Production Methods

Produced by chlorinating bis(2-ethylhexyl) phosphonate to give the phosphate diester chloride, followed by hydrolysis, or by saponification of tris(2-ethylhexyl) phosphate .

Synthesis

2-ethylhexan-1-ol could be used as a starting material to synthesize Bis(2-ethylhexyl) phosphate.

General Description

Odorless light yellow liquid. Floats on water.

Reactivity Profile

Organophosphates, such as Bis(2-ethylhexyl) phosphate, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides. Mildly corrosive to most metals; may form flammable hydrogen gas [USCG, 1999].

Health Hazard

Contact with liquid irritates eyes and may cause serious injury; consult an eye specialist. Also causes skin irritation on contact. Ingestion produces irritation similar to that caused by strong vinegar.

Fire Hazard

Special Hazards of Combustion Products: Irritating phosphorus oxides may be released.

Flammability and Explosibility

Non flammable

Purification Methods

Contaminants of commercial samples include the monoester, polyphosphates, pyrophosphate, 2-ethylhexanol and metal impurities. Dissolve the acid in n-hexane to give an 0.8M solution. Wash this with an equal volume of M HNO3, then with saturated (NH4)2CO3 solution, with 3M HNO3, and twice with water [Petrow & Allen Anal Chem 33 1303 1961]. Similarly, the impure sodium salt, after scrubbing with pet ether, is acidified with HCl and the free organic acid is extracted into pet ether and purified as above [Peppard et al. J Inorg Nucl Chem 7 231 1958], or as described by Stewart & Crandall [J Am Chem Soc 73 1377 1951]. It can be purified via its copper salt [McDowell et al. J Inorg Nucl Chem 38 2127 1976]. [Beilstein 1 IV 1796.]

Bis(2-ethylhexyl) phosphate Preparation Products And Raw materials

Raw materials

Preparation Products

Bis(2-ethylhexyl) phosphateSupplier

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