Substance
ID:306239
Names and Identifiers
IUPAC Traditional name
diethyl methylphosphonate
IUPAC name
diethyl methylphosphonate
Synonyms
DEMP双(二乙氧基氧膦基)甲烷Diethyl methylphosphonateDiethoxymethylphosphine oxideBis(diethoxyphosphinyl)methane甲基膦酸二乙酯
Registration numbers
MDL Number
CAS Number
Beilstein Number
EC Number
PubChem SID
Properties
Safety Information
Risk Statements
36/37/38
Safety Statements
26-36
Personal Protective Equipment
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Signal Word
Warning
GHS Hazard statements
H315-H319-H335
GHS Precautionary statements
P261-P305+P351+P338
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
MSDS Link
RTECS
SZ9085000
German water hazard class
3
European Hazard Symbols
Irritant (Xi)Product Information
Purity
97%
Linear Formula
CH3P(O)(OC2H5)2
Physical Property
Density
1.041 g/mL at 25 °C(lit.)
Refractive Index
n20/D 1.414(lit.)
Boiling Point
194 °C(lit.)
Flash Point
167 °F
75 °C
Molecule Details
Packaging
5, 25 g in glass bottle
Application
Reactant for the synthesis of:
• Fluoroalkyl α- and β-aminophosphonates1
• Acyclic nucleoside phosphonates with branched phosphonoethoxy-Et chains as potential antivirals2
• Difluoromethyl arylphosphonates3
• Pyridone alkaloids with neuritogenic activity4
• Lipophilic meropenem-derived prodrugs5
• Phomactin cyclohexane core and diterpenoid framework6
• Phosphonylated peptides via solid-phase synthesis7
Reagent employed in the synthesis of α-alkenyl, γ-hydroxyl, and dialkyl fluoroalkynyl phosphonates.
5, 25 g in glass bottle
Application
Reactant for the synthesis of:
• Fluoroalkyl α- and β-aminophosphonates1
• Acyclic nucleoside phosphonates with branched phosphonoethoxy-Et chains as potential antivirals2
• Difluoromethyl arylphosphonates3
• Pyridone alkaloids with neuritogenic activity4
• Lipophilic meropenem-derived prodrugs5
• Phomactin cyclohexane core and diterpenoid framework6
• Phosphonylated peptides via solid-phase synthesis7
Reagent employed in the synthesis of α-alkenyl, γ-hydroxyl, and dialkyl fluoroalkynyl phosphonates.
Molecular Spectra
No Data Available
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References
No Data Available
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