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Supelco

Bis(methylglycol) phthalate

analytical standard

Sinonimo/i:

Bis(2-methoxyethyl) phthalate, Dimethylglycol phthalate

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About This Item

Formula empirica (notazione di Hill):
C14H18O6
Numero CAS:
Peso molecolare:
282.29
Beilstein:
2056929
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. ebollizione

230 °C/10 mmHg (lit.)

Densità

1.173 g/mL at 20 °C (lit.)

applicazioni

cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Stringa SMILE

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
HSUIVCLOAAJSRE-UHFFFAOYSA-N

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Descrizione generale

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

Applicazioni

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.

Prodotti consigliati

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.

Pittogrammi

Health hazard

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Repr. 1B

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

249.8 °F - closed cup

Punto d’infiammabilità (°C)

121 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Certificati d'analisi (COA)

Lot/Batch Number

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I clienti hanno visto anche

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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

Articoli

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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