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Supelco

Bis(methylglycol) phthalate

analytical standard

Synonym(s):

Bis(2-methoxyethyl) phthalate, Dimethylglycol phthalate

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About This Item

Empirical Formula (Hill Notation):
C14H18O6
CAS Number:
117-82-8
Molecular Weight:
282.29
Beilstein/REAXYS Number:
2056929
EC Number:
204-212-6
MDL number:
MFCD00042842
UNSPSC Code:
41116107
PubChem Substance ID:
329755546
NACRES:
NA.24

grade

analytical standard

Quality Level

100

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

230 °C/10 mmHg (lit.)

density

1.173 g/mL at 20 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

SMILES string

COCCOC(=O)c1ccccc1C(=O)OCCOC

InChI

1S/C14H18O6/c1-17-7-9-19-13(15)11-5-3-4-6-12(11)14(16)20-10-8-18-2/h3-6H,7-10H2,1-2H3

InChI key

HSUIVCLOAAJSRE-UHFFFAOYSA-N

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General description

Bis(methylglycol) phthalate belongs to the class of phthalate esters widely used as plasticizers in plastic films.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support. Bis(methylglycol) phthalate may be used as an analytical reference standard for the quantification of the analyte in plastic food packaging materials using gas chromatography coupled to tandem mass spectrometry.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H360

Hazard Classifications

Repr. 1B

Storage Class

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

wgk_germany

WGK 1

flash_point_f

249.8 °F - closed cup

flash_point_c

121 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB3394
BCBT9573
BCBT5847
SZBD193XV
SZB9111XV

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Gas chromatography-triple quadrupole tandem mass spectrometry for successive single-surface migration study of phthalate esters from polythene film
Yang J, et al.
Food Control, 73, 1134-1143 (2017)
Yuki Ito et al.
Journal of occupational health, 49(3), 172-182 (2007-06-19)
Di(2-ethylhexyl)phthalate (DEHP), a commonly used industrial plasticizer, causes liver tumorigenesis presumably via activation of peroxisome proliferator-activated receptor alpha (PPARalpha). The mechanism of DEHP tumorigenesis has not been fully elucidated, and to clarify whether DEHP tumorigenesis is induced via PPARalpha, we
J Yonemoto et al.
Toxicology letters, 21(1), 97-102 (1984-04-01)
The secondary metabolite of dimethoxyethyl phthalate (DMEP), methoxyacetic acid (MAA), but neither the diester nor either of its primary metabolites, monomethoxyethyl phthalate (MMEP) and 2-methoxyethanol (ME), interferes with normal growth and development of organogenesis phase rat embryos in culture. These
E J Ritter et al.
Teratology, 32(1), 25-31 (1985-08-01)
It is hypothesized that the known teratogen di(2-methoxyethyl) phthalate (DMEP) acts by in vivo hydrolysis to 2-methoxyethanol (2-ME), also a known teratogen, which in turn is metabolized to methoxyacetic acid (MAA), the proximate teratogen. Teratological studies were conducted with Wistar
M R Parkhie et al.
Environmental health perspectives, 45, 89-97 (1982-11-01)
A single intraperitoneal injection (0.6 ml/kg) of dimethoxyethyl phthalate (DMEP) was given to groups of Wistar strain rats on day 10, 11, 12, 13 or 14 of gestation. Control rats received 0.6 ml/kg of physiological saline intraperitoneally. In phthalate-treated rats
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Articles

SPME-GC-MS Determination of Phthalate Esters in Ramen Noodle Flavor Packets

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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