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线性分子式:
HCO2CH3
化学文摘社编号:
分子量:
60.05
UNSPSC Code:
12352108
NACRES:
NA.21
PubChem Substance ID:
EC Number:
203-481-7
Beilstein/REAXYS Number:
1734623
MDL number:
Grade:
spectrophotometric grade
Assay:
≥98%
Technique(s):
UV/Vis spectroscopy: suitable
Bp:
32-34 °C (lit.)
Vapor pressure:
32.81 psi ( 55 °C)
9.21 psi ( 20 °C)
9.21 psi ( 20 °C)
产品名称
甲酸甲酯, spectrophotometric grade, ≥98%
InChI key
TZIHFWKZFHZASV-UHFFFAOYSA-N
InChI
1S/C2H4O2/c1-4-2-3/h2H,1H3
SMILES string
[H]C(=O)OC
grade
spectrophotometric grade
vapor density
2.1 (vs air)
vapor pressure
32.81 psi ( 55 °C)
9.21 psi ( 20 °C)
assay
≥98%
form
liquid
autoignition temp.
842 °F
expl. lim.
23 %
technique(s)
UV/Vis spectroscopy: suitable
impurities
<0.05% water
evapn. residue
<0.0005%
refractive index
n20/D 1.343 (lit.)
pH
4.0-5.0 (20 °C, 200 g/L)
bp
32-34 °C (lit.)
mp
−100 °C (lit.)
density
0.974 g/mL at 20 °C (lit.)
λ
H2O reference
UV absorption
λ: 259 nm Amax: 1.00
λ: 260 nm Amax: 0.70
λ: 265 nm Amax: 0.20
λ: 270 nm Amax: 0.04
λ: 310-400 nm Amax: 0.1
Quality Level
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Application
- Bifunctionality of Re Supported on TiO(2) in Driving Methanol Formation in Low-Temperature CO(2) Hydrogenation.: This article explores the catalytic roles of methyl formate in methanol production from CO2 hydrogenation, providing a pathway for sustainable chemical synthesis (Urakawa A et al., 2023).
General description
Methyl formate (MF) is one of the most significant intermediates in C1 chemistry. MF has been used to produce methanamide, N, N-dimethylformamide, dimethyl carbonate, methyl glycolate, acetic acid, ethylene glycol, methyl methacrylate, and high-purity CO. Additionally, MF can be used as a solvent for nitrocellulose and cellulose acetate.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 1 - STOT SE 1 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
-2.2 °F - closed cup
flash_point_c
-19 °C - closed cup
法规信息
新产品
此项目有
Katherine R Phillips et al.
Journal of the American Chemical Society, 135(2), 574-577 (2012-12-28)
Methyl formate is produced from the photo-oxidation of methanol on preoxidized TiO(2)(110). We demonstrate that two consecutive photo-oxidation steps lead to methyl formate using mass spectrometry and scanning tunneling microscopy. The first step in methanol oxidation is formation of methoxy
Methyl N-Phenyl Carbamate Synthesis from Aniline and Methyl Formate: Carbon Recycling to Chemical Products.
Yalfani MS, et al.
ChemSusChem, 8(3), 443-447 (2015)
Barriers to rotation adjacent to double bonds. 3. The carbon-oxygen barrier in formic acid, methyl formate, acetic acid, and methyl acetate. The origin of ester and amide resonance.
Wiberg KB and Laidig KE.
Journal of the American Chemical Society, 109(20), 5935-5943 (1987)
Methyl formate as a carbonylating agent for the catalytic conversion of phenol to methyl phenyl carbonate.
Wu C, et al.
Green Chemistry, 17(3), 1467-1472 (2015)
Microwave spectrum, barrier to internal rotation, and structure of methyl formate.
Curl Jr RF.
J. Chem. Phys. , 30(6), 1529-1536 (1959)
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