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132195

Sigma-Aldrich

Trimethyl phosphate

97%

Sinônimo(s):

TMP, TMPA, TMPO

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About This Item

Fórmula linear:
(CH3O)3PO
Número CAS:
512-56-1
Peso molecular:
140.07
Beilstein:
1071731
Número CE:
208-144-8
Número MDL:
MFCD00008348
Código UNSPSC:
12352100
ID de substância PubChem:
24847552
NACRES:
NA.22

Nível de qualidade

200

Ensaio

97%

Formulário

liquid

índice de refração

n20/D 1.395 (lit.)

p.e.

197 °C (lit.)

pf

−46 °C (lit.)

densidade

1.197 g/mL at 25 °C (lit.)

grupo funcional

phosphate

cadeia de caracteres SMILES

COP(=O)(OC)OC

InChI

1S/C3H9O4P/c1-5-8(4,6-2)7-3/h1-3H3

chave InChI

WVLBCYQITXONBZ-UHFFFAOYSA-N

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Descrição geral

Trimethyl phosphate is an excellent dipolar aprotic solvent that is used as a methylating agent and acid scavenger in many organic transformations.

Aplicação

Trimethyl phosphate can be used as a methylating agent for the:
  • Solvent-free o-methylation of phenolic compounds to synthesize methyl aryl ethers.
  • S-methylation of aryl/alkyl thiols to synthesize S-methylated product in the presence of Ca(OH)2 as a base.

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Danger

Frases de perigo

H302,H315,H319,H340,H351

Classificações de perigo

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Muta. 1B - Skin Irrit. 2

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

302.0 °F - closed cup

Ponto de fulgor (°C)

150 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
MKCQ7593
MKCQ0590
MKCP4616
MKCN7206
MKCN4674

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Hydrolysis of acetyl dimethyl phosphate, a reactive acyl phosphate.
R Kluger et al.
Biochemistry, 11(8), 1544-1546 (1972-04-11)
Yongqing Ma et al.
Analytica chimica acta, 786, 47-53 (2013-06-26)
An analytical method for the determination of 14 organophosphorus flame retardants (OPFRs), including halogenated OPFRs, non-halogenated OPFRs and triphenyl phosphine oxide (TPPO) in biological samples was developed using gas chromatography-mass spectrometry (GC/MS). Biological samples were extracted using microwave-assisted extraction (MAE)
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
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
Chunhai Ruan et al.
Journal of the American Society for Mass Spectrometry, 19(2), 305-314 (2008-04-15)
Threshold collision-induced dissociation techniques are employed to determine the bond dissociation energies (BDEs) of complexes of alkali metal cations to trimethyl phosphate, TMP. Endothermic loss of the intact TMP ligand is the only dissociation pathway observed for all complexes. Theoretical
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Global Trade Item Number

SKUGTIN
83850-25G4061833417881
R3629-1G
R6625-25G4061836695927
R6625-500G
R6750-1G4061836695941
R6750-250MG4061833290026
R6750-500MG4061833290033
R6875-1G4061836695958
R6875-5G
83850-100G4061833005859
R6625-100G4061836695903
R6625-1KG4061836695910
R6750-100MG4061836695934
R6875-100MG
R3629-25G4061836695088
R3629-5G4061833663639
132195-1KG4061838728890
132195-250G4061838728906

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