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31301

Supelco

Dioctyl phthalate

analytical standard

Synonyme(s) :

Phthalic acid di-n-octyl ester

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About This Item

Formule empirique (notation de Hill):
C24H38O4
Numéro CAS:
Poids moléculaire :
390.56
Numéro Beilstein :
1915994
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Densité

0.980 g/mL at 20 °C (lit.)

Application(s)

cleaning products
cosmetics
food and beverages
personal care

Format

neat

Chaîne SMILES 

CCCCCCCCOC(=O)c1ccccc1C(=O)OCCCCCCCC

InChI

1S/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

Clé InChI

MQIUGAXCHLFZKX-UHFFFAOYSA-N

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Description générale

Di-n-octyl phthalate, belonging to the class of plasticizers, is found to be omnipresent in the environment. It is reported to be used in the manufacturing of flooring tiles, bottle cap liners, indirect food additives and toys.
Di-n-octyl phthalate (DNOP) is a mixed component of C6–C10 linear-chain phthalates which has the ability to impart flexibility in plastics and rubber materials. It is also used as plasticizer in PVC used in flooring and carpet tiles.

Application

DNOP has been used as standard during solid-phase microextraction followed by GC-MS analysis of phthalate esters in water sample examined after sonochemical degradation.
Di-n-octyl phthalate may be used as an analytical reference standard for the quantification of the analyte in:
  • Soil samples using micellar electro-kinetic chromatography (MEKC), further confirmed by gas chromatography with flame ionization detection (GC-FID).
  • Bottled water using gas chromatography coupled to mass spectrometry (GC-MS).
  • Plastic toys using gas chromatography with flame ionization detection (GC-FID).

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Mentions de danger

Conseils de prudence

Classification des risques

Aquatic Chronic 4

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

228.2 °F - closed cup

Point d'éclair (°C)

109.0 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Certificats d'analyse (COA)

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Les clients ont également consulté

Mono-(3-carboxypropyl) phthalate, a metabolite of di-n-octyl phthalate.
Calafat AM
Journal of Toxicology and Environmental Health. Part A, 69(3-4), 215-227 (2006)
Subchronic oral toxicity of di-n-octyl phthalate and di(2-Ethylhexyl) phthalate in the rat.
Poon R
Food And Chemical Toxicology, 35(2), 225-239 (1997)
Separation and determination of phthalates by micellar electrokinetic chromatography
Guo BY, et al.
Journal of Chromatography A, 1095(1-2), 189-192 (2005)
P Wang et al.
Chemosphere, 72(10), 1567-1572 (2008-06-13)
Phthalic acid esters (PAEs) are used in many branches of industry and are produced in huge amounts throughout the world. An investigation on particulate- and gas-phase distribution of PAEs has been conducted in Nanjing (China). The 12-h daily sampling program
Xueling Wu et al.
Journal of hazardous materials, 176(1-3), 262-268 (2009-12-05)
Two bacterial strains were isolated from activated sludge using mixtures of phthalic acid esters (PAEs) as the sole source of carbon and energy. One of the isolates was identified as Gordonia sp. strain JDC-2 and the other as Arthrobacter sp.

Articles

A sensitive, quantitative, and reproducible SPME-GC/MS procedure was developed by Supelco for the extraction of phthalate esters from oily food matrices, such as the flavored oils included with ramen noodle kits.

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