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Merck

36735

Phtalate de bis(2-éthylhexyle)

PESTANAL®, analytical standard

Synonyme(s) :

Bis(2-éthylhexyl ester) d’acide phthalique

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A propos de cet article

Formule empirique (notation de Hill) :
C24H38O4
Numéro CAS:
117-81-7
Poids moléculaire :
390.56
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755483
EC Number:
204-211-0
Beilstein/REAXYS Number:
1890696
MDL number:
MFCD00009493

Principaux documents

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Nom du produit

Phtalate de bis(2-éthylhexyle), PESTANAL®, analytical standard

InChI key

BJQHLKABXJIVAM-UHFFFAOYSA-N

InChI

1S/C24H38O4/c1-5-9-13-19(7-3)17-27-23(25)21-15-11-12-16-22(21)24(26)28-18-20(8-4)14-10-6-2/h11-12,15-16,19-20H,5-10,13-14,17-18H2,1-4H3

SMILES string

CCCCC(CC)COC(=O)c1ccccc1C(=O)OCC(CC)CCCC

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

386 °C (lit.)

density

0.985 g/mL at 20 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

Quality Level

100

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Catégories apparentées

Application

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

General description

This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H360FD

Hazard Classifications

Repr. 1B

Classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 1

flash_point_f

392.0 °F - Pensky-Martens closed cup

flash_point_c

200 °C - Pensky-Martens closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificats d'analyse (COA)

Lot/Batch Number
BCCK6225
BCCK6224
BCCK6223
BCCC8985
BCBX5578

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Jian Hou et al.
Ecotoxicology and environmental safety, 182, 109384-109384 (2019-07-05)
Exposure to polycyclic aromatic hydrocarbons (PAHs) and phthalates link to oxidative stress and inflammatory response, which exert cellular aging. However, modification effect of seasonal factor on the association of PAHs or phthalates exposure with relative telomere length (RTL) or mitochondrial
Alessia Arena et al.
Food chemistry, 396, 133721-133721 (2022-07-24)
Phthalic acid esters (PAEs), known as phthalates, have a variety of industrial applications, mainly related to their ability to increase plastic softness,flexibility, and durability. With regard to toxicological aspects, several studies suggest that phthalates would act as endocrine-disrupting chemicals, and
N B Hopf et al.
Toxicology letters, 224(1), 47-53 (2013-10-22)
Phthalates are suspected to be endocrine disruptors. Di(2-ethylhexyl) phthalate (DEHP) is assumed to have low dermal absorption; however, previous in vitro skin permeation studies have shown large permeation differences. Our aims were to determine DEHP permeation parameters and assess extent
Na Rae Song et al.
Environment international, 54, 65-73 (2013-02-19)
Di(2-ethylhexyl) phthalate (DEHP) is one of the common phthalate plasticizers used primarily in soft polyvinyl chloride, which is a plastic polymer that makes up the total weight of goods from 1% up to 40% in many consumer products. The aims
Outi Huttala et al.
ALTEX, 36(3), 419-434 (2019-03-18)
Besides being an energy storage, adipose tissue is an endocrine organ closely associated with vascular system. Human relevant in vitro models are needed to study adipose tissue and related diseases. Vasculature plays a central role in the development and inhibition
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