Dioctyl phthalate(DOP)

Basic information

  • Product Name:Dioctyl phthalate(DOP)
  • CasNo.:117-84-0
  • MF:C24H38O4
  • MW:390.563

Physical and Chemical Properties

  • Purity:99%
  • Boiling Point:-25 °C
  • Packing:clear liquid with a mild odor
  • Throughput:
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Product Details

CasNo: 117-84-0

MF: C24H38O4

Appearance: clear liquid with a mild odor

Buy reliable Quality Dioctyl phthalate(DOP) 117-84-0 raw material with Honest Price

  • Molecular Formula:C24H38O4
  • Molecular Weight:390.563
  • Appearance/Colour:clear liquid with a mild odor 
  • Vapor Pressure:5(x 10-8 mmHg) at 82 °C, 500 at 132 °C (Gross and Colony, 1973) 
  • Melting Point:-25 °C 
  • Refractive Index:n20/D 1.485  
  • Boiling Point:416.4 °C at 760 mmHg 
  • Flash Point:222.3 °C 
  • PSA:52.60000 
  • Density:0.985 g/cm 
  • LogP:6.72120 

DI-N-OCTYL PHTHALATE(Cas 117-84-0) Usage

Physical properties

Clear, light colored, viscous, oily liquid with a slight odor

General Description

A clear liquid with a mild odor. Slightly less dense than water and insoluble in water. Hence floats on water. Flash point 430°F. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. As a liquid, can easily penetrate the soil and contaminate groundwater and nearby streams. Eye contact may produce severe irritation and direct skin contact may produce mild irritation. Used in the manufacture of a variety of plastics and coating products.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

DI-N-OCTYL PHTHALATE reacts 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 with caustic solutions. Flammable hydrogen may be generated by mixing with alkali metals and hydrides. Can generate electrostatic charges by swirling or pouring [Handling Chemicals Safely, 1980. p. 250].

Health Hazard

Produces no ill effects at normal temperatures but may give off irritating vapor at high temperature.

Fire Hazard

Special Hazards of Combustion Products: None

Safety Profile

Mildly toxic by ingestion. Experimental teratogenic and reproductive effects. A skin and severe eye irritant. Used as a plasticizer. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.

Source

Detected in distilled water-soluble fractions of new and used motor oil at concentrations of 1.3 to 1.4 and 73 to 78 μg/L, respectively (Chen et al., 1994). May leach from plastic products (e.g., tubing, containers) used in laboratories during chemical analysis of aqueous samples.

Environmental fate

Biological. o-Phthalic acid was tentatively identified as the major degradation product of di-noctyl phthalate produced by the bacterium Serratia marcescens (Mathur and Rouatt, 1975). When di-n-octyl phthalate was statically incubated in the dark at 25 °C with yeast extract and settled domestic wastewater inoculum, no degradation was observed after 7 d. In a 21-d period, however, gradual adaptation did occur, resulting in 94 and 93% losses at concentrations of 5 and 10 mg/L, respectively (Tabak et al., 1981). In the presence of suspended natural populations from unpolluted aquatic systems, the second-order microbial transformation rate constant determined in the laboratory was reported to be 3.7 ± 0.6 x 10-13 L/organism?h (Steen, 1991). Chemical/Physical. Under alkaline conditions, di-n-octyl phthalate will initially hydrolyze to noctyl hydrogen phthalate and 1-octanol. The monoester will undergo hydrolysis forming ophthalic acid and 1-octanol (Kollig, 1993). The hydrolysis half-life at pH 7 and 25 °C was estimated to be 107 yr (Ellington et al., 1988).

InChI:InChI=1/C24H38O4/c1-3-5-7-9-11-15-19-27-23(25)21-17-13-14-18-22(21)24(26)28-20-16-12-10-8-6-4-2/h13-14,17-18H,3-12,15-16,19-20H2,1-2H3

117-84-0 Relevant articles

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Bobkova,Stokolos,Garifullin

, p. 336 - 340 (2019/08/15)

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Paragraph 0018; 0019; 0020; 0021; 0023; 0024; 0025-0031, (2017/05/23)

The invention relates to a production pr...

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Parmar, Ajay M,Saravanan,Tyagi, Beena,Srinivasan, Kannan

, p. 747 - 755 (2017/08/04)

The present study reports the synthesis ...

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Page/Page column 20, (2016/06/20)

The present invention relates to a novel...

117-84-0 Process route

phthalic anhydride
85-44-9

phthalic anhydride

octanol
111-87-5

octanol

Di-n-octyl phthalate
117-84-0,8031-29-6

Di-n-octyl phthalate

Mono-n-octyl phthalate
5393-19-1

Mono-n-octyl phthalate

Conditions
Conditions Yield
With montmorillonite K-10; In tetrachloromethane; at 76 ℃; for 12h;
54%
21%
n-heptane
142-82-5

n-heptane

pyrene
129-00-0

pyrene

naphthalene
91-20-3,71998-51-1,72931-45-4

naphthalene

biphenyl
92-52-4,1594-86-1

biphenyl

2-phenylnaphthalene
612-94-2

2-phenylnaphthalene

phenanthrene
85-01-8

phenanthrene

anthracene
120-12-7

anthracene

fluoranthene
206-44-0

fluoranthene

Di-n-octyl phthalate
117-84-0,8031-29-6

Di-n-octyl phthalate

acenaphthene
83-32-9

acenaphthene

acenaphthylene
208-96-8,25036-01-5

acenaphthylene

Conditions
Conditions Yield
Mechanism; Microwave irradiation;

117-84-0 Upstream products

  • 85-44-9
    85-44-9

    phthalic anhydride

  • 111-87-5
    111-87-5

    octanol

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    84-66-2

    Diethyl phthalate

  • 88-99-3
    88-99-3

    benzene-1,2-dicarboxylic acid

117-84-0 Downstream products

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    88-99-3

    benzene-1,2-dicarboxylic acid

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    5393-19-1

    Mono-n-octyl phthalate

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    1121-84-2

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