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Supelco

Dimethylphthalat -Lösung

certified reference material, 5000 μg/mL in methanol

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About This Item

CAS-Nummer:
131-11-3
EG-Nummer:
200-659-6
UNSPSC-Code:
41116105

Qualität

certified reference material
TraceCERT®

Produktlinie

TraceCERT®

Analysenzertifikat (CofA)

current certificate can be downloaded

Verpackung

ampule of 1 mL

Konzentration

5000 μg/mL in methanol

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Anwendung(en)

cleaning products
cosmetics
environmental
food and beverages
personal care

Format

single component solution

Lagertemp.

2-8°C

InChI

1S/C10H10O4/c1-13-9(11)7-5-3-4-6-8(7)10(12)14-2/h3-6H,1-2H3

InChIKey

NIQCNGHVCWTJSM-UHFFFAOYSA-N

Anwendung

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

Sonstige Hinweise

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Rechtliche Hinweise

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

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Zielorgane

Eyes

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

51.8 °F - closed cup

Flammpunkt (°C)

11 °C - closed cup

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
LRAD2456
LRAC2867
XA19097V
XA19096V
XA10180V

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Zhujian Huang et al.
Journal of hazardous materials, 246-247, 70-78 (2013-01-05)
The organic layered double hydroxides (LHDs)/TiO(2) composites with various mass ratios were prepared by the reconstruction of mixed metal oxides to photodegrade dimethyl phthalate (DMP). The physicochemical properties of the obtained products were analyzed by X-ray diffraction (XRD) spectra, X-ray
Guy Bouchoux et al.
The journal of physical chemistry. A, 114(27), 7408-7416 (2010-06-22)
Aromatic substitution reactions of selected ionized benzenes derivatives (chlorobenzene, nitrobenzene, dimethylphtalates) and phenoxy cation using neutral methyl isocyanide as a nucleophile are shown to efficiently occur in the gas phase. Nitrilium ions are produced in high abundance during these processes.
Elijah J Petersen et al.
Environmental toxicology and chemistry, 30(4), 988-996 (2011-02-11)
The effects of loading and aging pyrene in soils in the presence of four environmentally common nonaqueous-phase liquids (NAPLs) (hexadecane, 2,2,4,4,6,8,8-heptamethylnonane [HMN], toluene, and dimethyl phthalate [DMP]) on its subsequent desorption from those soils, earthworm accumulation, biodegradation, and extractability were
Wenxin Wang et al.
Environmental monitoring and assessment, 184(11), 6789-6798 (2011-12-08)
Atmospheric trace phthalic esters (PAEs) carried by total suspended particulates were systematically investigated. A total of 450 air samples were collected at six typical locations and three specific micro-environmental sites (a stadium with a new plastic track, new cars, and
L J Xu et al.
Water research, 47(6), 1996-2004 (2013-02-12)
The merits of the combined process of high-frequency ultrasound (US) and catalyst-free ultraviolet irradiation (UV) have been evaluated in this study by investigating the sonophotolytic degradation of dimethyl phthalate (DMP). A 400 kHz ultrasonic system and a photolytic system at
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