241024
Trimethyl phosphate
≥99%
Synonym(s):
TMP, TMPA, TMPO
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About This Item
Linear Formula:
(CH3O)3PO
CAS Number:
Molecular Weight:
140.07
Beilstein:
1071731
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥99%
form
liquid
refractive index
n20/D 1.395 (lit.)
bp
197 °C (lit.)
mp
−46 °C (lit.)
density
1.197 g/mL at 25 °C (lit.)
SMILES string
COP(=O)(OC)OC
InChI
1S/C3H9O4P/c1-5-8(4,6-2)7-3/h1-3H3
InChI key
WVLBCYQITXONBZ-UHFFFAOYSA-N
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General description
The trimethyl phosphate levels in environmental water was determined by direct analysis real-time ionization source interfaced with a triple quadrupole mass spectrometer (DART-MS/MS) with multiple reaction monitoring (MRM).
Application
- Enhanced Battery Performance: Trimethyl phosphate is utilized to manipulate the ionic conductivity and interfacial compatibility in polymer-in-dual-salt electrolytes, significantly extending the operable temperature range of quasi-solid metal batteries (Lin et al., 2024).
- Thermochemical Properties Analysis: Research on trimethyl phosphate′s thermochemistry properties and rate kinetics, particularly H-Atom Abstraction reactions, provides valuable insights into its stability and reactivity, which are crucial for various chemical synthesis applications (Bruce and Li, 2023).
- Organophosphorus Flame Retardants Detection: Trimethyl phosphate is explored for its role in the screening of organophosphorus flame retardant residues in food samples, specifically rice, utilizing advanced chromatographic techniques to ensure food safety and compliance with environmental regulations (Li et al., 2023).
- Interfacial Reaction Regulation in Batteries: The study on regulating interfacial reactions through electrolyte chemistry, involving trimethyl phosphate, highlights its potential to create gradient interphases for low-temperature zinc metal batteries, contributing to enhanced battery safety and efficiency (Wang et al., 2023).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Muta. 1B - Skin Irrit. 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 1
Flash Point(F)
302.0 °F - closed cup
Flash Point(C)
150 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Xiaowei Wang et al.
Journal of chromatography. A, 1333, 134-137 (2014-02-20)
Trimethyl phosphate (TMP) is used extensively in industrial chemical processes. Due to the high polarity and volatility, methods for its quantification in environmental samples have not been well developed. Currently, the pollution status of TMP in the environment still has
R V Banerjee et al.
Biochemistry, 27(25), 9062-9070 (1988-12-13)
The transfer of 17O and/or 18O from (COOH-17O or -18O) enriched substrates to inorganic phosphate (Pi) has been demonstrated for two enzyme-catalyzed reactions involved in folate biosynthesis and glutamylation. COOH-18O-labeled folate, methotrexate, and dihydropteroate, in addition to [17O]-glutamate, were synthesized
Qingguo Meng et al.
Environmental science & technology, 45(7), 3000-3005 (2011-03-03)
Due to the neurotoxicity of organophosphate (OP) pesticides and nerve agents synthesized as military or terror agents, their safe destruction and disposal is of considerable current importance. A representative OP, trimethyl phosphate (TMP), was adsorbed onto NaX zeolite, two mesoporous
K Sundararajan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(10), 1855-1867 (2000-09-16)
Trimethyl phosphate (TMP) and acetylene were codeposited in nitrogen and argon matrices and adducts of these species were identified using infrared spectroscopy. Formation of the adducts was evidenced by shifts in the vibrational frequencies of the modes involving the TMP
Johannes Bernarding et al.
Journal of the American Chemical Society, 128(3), 714-715 (2006-01-19)
In ultralow magnetic fields, liquid state nuclear magnetic resonance (NMR) spectra of homonuclear spin systems exhibit line widths dominated by their natural lifetime. Chemical shifts become negligible, and heteronuclear NMR spectra show predominantly the electron-mediated field-independent J-coupling. However, weak polarization
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