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80135

Supelco

Diisodecyl phthalate

Selectophore™, ≥99.0%

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About This Item

Formula empirica (notazione di Hill):
C28H46O4
Numero CAS:
26761-40-0
Peso molecolare:
446.66
Beilstein:
2171889
Numero CE:
247-977-1
Codice UNSPSC:
26111700
ID PubChem:
329768722
NACRES:
NB.61

Grado

for ion-selective electrodes

Livello qualitativo

200

Nome Commerciale

Selectophore™

Saggio

≥99.0% (sum of isomers, GC)
≥99.0%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.486

Densità

0.965 g/mL at 20 °C (lit.)

Stringa SMILE

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
ZVFDTKUVRCTHQE-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

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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Applicazioni

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

Note legali

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Indicazioni di pericolo

H413

Consigli di prudenza

P273 - P501

Classi di pericolo

Aquatic Chronic 4

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

527.0 °F - closed cup

Punto d’infiammabilità (°C)

275.00 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCD6089
BCCC2160
BCCB5408
BCCB0561
BCBT7846

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Sigma-Aldrich

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Sigma-Aldrich

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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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