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89353

Supelco

Density Standard 1191 kg/m3

H&D Fitzgerald Ltd. Quality

Synonym(s):

Dimethyl phthalate, DMP

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About This Item

Linear Formula:
C6H4-1,2-(CO2CH3)2
CAS Number:
131-11-3
Molecular Weight:
194.18
Beilstein:
1911460
EC Number:
205-011-6
MDL number:
MFCD00008425
UNSPSC Code:
41116107
PubChem Substance ID:
329769726
NACRES:
NA.24

grade

analytical standard

autoignition temp.

1033 °F

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

H&D Fitzgerald Ltd.

refractive index

n20/D 1.515 (lit.)

bp

282 °C (lit.)

mp

2 °C (lit.)

density

1.19 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
industrial qc
personal care
petroleum
pharmaceutical (small molecule)

format

mixture

SMILES string

COC(=O)c1ccccc1C(=O)OC

InChI

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

InChI key

NIQCNGHVCWTJSM-UHFFFAOYSA-N

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Application

This density CRM is used for the calibration of all types of laboratory density meters in the test temperature range of 10 to 50 °C.

Features and Benefits

  • Manufactured and verified in an ISO 17025 accredited laboratory, as per UKAS
  • Carries an associated uncertainty of +/- 0.010 Kg/m3
  • Provided in a sealed glass ampoule of 10 mL to assure safe delivery
  • Accompanied with a certificate of analysis (CoA) having information on the expiry date for an effective audit

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

294.8 °F - closed cup

Flash Point(C)

146.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCL0656
BCCK7508
BCCK0381
BCCJ6084
BCCH3264

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Diethyl phthalate PESTANAL®, analytical standard

Supelco

53008

Diethyl phthalate

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.
Yi-Hung Chen et al.
Journal of hazardous materials, 192(3), 1017-1025 (2011-07-05)
The removal of dimethyl phthalate (DMP), which is a pollutant of concern in water environments, was carried out by catalytic ozonation with TiO(2)/Al(2)O(3) catalysts. The heterogeneous catalytic ozonation was an ozonation process combined with the catalytic and adsorptive properties of
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
Yiling Chen et al.
Journal of hazardous materials, 235-236, 92-100 (2012-08-14)
In this study, we demonstrate that the decomposition of dimethyl phthalate under microwave irradiation could be greatly enhanced over Fe@Fe(2)O(3) nanowires supported on activated carbon (Fe@Fe(2)O(3)/AC). The great enhanced decomposition of dimethyl phthalate could be attributed to a unique microwave
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