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Diisodecyl phthalate

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Diisodecyl phthalate Basic information

Product Name:
Diisodecyl phthalate
Synonyms:
  • DIDP
  • Diisodecyl-o-phthalate
  • DIISODEYLPHTHALATE
  • PHTHALIC ACID, BIS-ISODECYL ESTER
  • PHTHALIC ACID DIISODECYL ESTER
  • Diisodecyl Phthtalate
  • Diisodecyl phthalate
  • Diisodecyl phthalate 10g [26761-40-0]
CAS:
26761-40-0
MF:
C28H46O4
MW:
446.66
EINECS:
247-977-1
Product Categories:
  • Functional Materials
  • Phthalates (Plasticizer)
  • Plasticizer
  • Analytical/Chromatography
  • Ion Sensor Materials
  • Plasticizer for ISE
Mol File:
26761-40-0.mol
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Diisodecyl phthalate Chemical Properties

Melting point:
235°C
Boiling point:
475.97°C (rough estimate)
Density 
0.965 g/mL at 20 °C (lit.)
vapor pressure 
0.1 hPa (20 °C)
refractive index 
n20/D 1.486
Flash point:
235 °C
storage temp. 
Store below +30°C.
solubility 
0.00028g/l
form 
Oil
color 
Colourless
Odor
Faint.
Water Solubility 
0.28mg/L(24 ºC)
BRN 
2171889
LogP
10.554 (est)
CAS DataBase Reference
26761-40-0(CAS DataBase Reference)
NIST Chemistry Reference
1,2-Benzenedicarboxylic acid, diisodecyl ester(26761-40-0)
EPA Substance Registry System
Diisodecyl phthalate (26761-40-0)
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Safety Information

Hazard Codes 
N
Risk Statements 
50/53
Safety Statements 
23-24/25-61-60
RIDADR 
UN 3082 9 / PGIII
WGK Germany 
1
RTECS 
TI1270000
Autoignition Temperature
380 °C
HS Code 
2917 33 00
Hazardous Substances Data
26761-40-0(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: > 5000 mg/kg LD50 dermal Rabbit > 3160 mg/kg

MSDS

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Diisodecyl phthalate Usage And Synthesis

Uses

Diisodecyl Phthalate is a phthalate plasticizer. Not only are pthalate plasticizers widely used in the plastics industry, but they have also been detected in soft drinks, pharmaceuticals and food products

Definition

ChEBI: Diisodecyl phthalate is a phthalate ester and a diester. Used as plasticizer for polyvinyl chloride in calendered film, coated fabrics, building wire jackets, wire and cable extrusion, and other applications.

Preparation

Diisodecyl phthalate is prepared from propylene and butenes through an oligomerisation process forming hydrocarbons with 8 to 15 carbon atoms. After distillation (in view of obtaining nonene), oxonation forms aldehydes with one more carbon atom ("isodecanal"). The latter are hydrogenated and distilled to form monohydric alcohols (mainly C10). These are reacted with phthalic anhydride (PA). The first reaction step, alcoholysis of PA to give the monoester, is rapid and goes to completion. By charging in excess alcohol and by removing the water which is formed, the equilibrium can be shifted almost completely towards the products side.

General Description

Diisodecyl phthalate appears as colorless liquid. May float or sink in?water. (USCG, 1999)

Air & Water Reactions

bis(8-methylnonyl) phthalate is insoluble in water.

Reactivity Profile

bis(8-methylnonyl) phthalate is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Can generate electrostatic charges. [Handling Chemicals Safely 1980. p. 250].

Health Hazard

No symptoms reported for any rate of exposure.

Fire Hazard

bis(8-methylnonyl) phthalate is combustible.

Diisodecyl phthalateSupplier

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