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Diisodecyl phthalate

Selectophore™, ≥99.0%

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About This Item

Empirical Formula (Hill Notation):
C28H46O4
CAS Number:
26761-40-0
Molecular Weight:
446.66
Beilstein:
2171889
EC Number:
247-977-1
UNSPSC Code:
26111700
PubChem Substance ID:
329768722
NACRES:
NB.61

grade

for ion-selective electrodes

Quality Level

200

product line

Selectophore™

Assay

≥99.0% (sum of isomers, GC)
≥99.0%

form

liquid

refractive index

n20/D 1.486

density

0.965 g/mL at 20 °C (lit.)

SMILES string

O=C(OCCCCCCCC(C)C)C1=C(C(OCCCCCCCC(C)C)=O)C=CC=C1

InChI

1S/C28H46O4/c1-23(2)17-11-7-5-9-15-21-31-27(29)25-19-13-14-20-26(25)28(30)32-22-16-10-6-8-12-18-24(3)4/h13-14,19-20,23-24H,5-12,15-18,21-22H2,1-4H3

InChI key

ZVFDTKUVRCTHQE-UHFFFAOYSA-N

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General description

Diisodecyl phthalate (DIDP) is a dialkyl or aryl/alkyl diesters of phthalic acid that belongs to phthalate group. It is mostly used as a plasticizer in the manufacturing of PVC membrane electrodes.
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Application

DIDP is used to quantify the analyte in urban stormwater, stormwater sediment, and snow samples by electrochemical and chromatography methods.

Legal Information

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Hazard Statements

H413

Precautionary Statements

P273 - P501

Hazard Classifications

Aquatic Chronic 4

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

527.0 °F - closed cup

Flash Point(C)

275.00 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCD6089
BCCC2160
BCCB5408
BCCB0561
BCBT7846

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Jae-Min Park et al.
Journal of basic microbiology, 49 Suppl 1, S31-S35 (2009-03-27)
In this study, diisodecyl phthalate (DIDP) was efficiently degraded by Bacillus sp. SB-007. The optimal conditions for DIDP (100 mg l(-1)) degradation by Bacillus sp. SB-007 in a mineral salts medium were found to be pH 7.0 at 30 degrees
Temperature and pressure dependence of the viscosities of 2-ethylhexyl benzoate, bis (2-ethylhexyl) phthalate, 2, 6, 10, 15, 19, 23-hexamethyltetracosane (squalane), and diisodecyl phthalate.
Harris, Kenneth R.
Journal of Chemical and Engineering Data, 54.9, 2729-2738 (2009)
Matthias Wormuth et al.
Risk analysis : an official publication of the Society for Risk Analysis, 26(3), 803-824 (2006-07-13)
Phthalic acid esters (phthalates) are used as plasticizers in numerous consumer products, commodities, and building materials. Consequently, phthalates are found in human residential and occupational environments in high concentrations, both in air and in dust. Phthalates are also ubiquitous food
Katell Fiselier et al.
Journal of separation science, 28(16), 2144-2152 (2005-12-02)
Injector-internal thermal desorption from edible oil or fat is a convenient sample preparation technique for the analysis of solutes in lipids or extracts from fatty foods. The injector temperature is selected to vaporize the solutes of interest while minimizing evaporation
R H McKee et al.
Journal of applied toxicology : JAT, 20(6), 491-497 (2001-02-17)
Recently there have been reports of liver and kidney tumors in rodents following long-term exposure to di(isononyl) phthalate (DINP). Mechanistic studies suggested that the liver tumors were a consequence of peroxisomal proliferation, whereas the kidney tumors (found only in male
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