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Fórmula lineal:
O(COOC2H5)2
Número CAS:
Peso molecular:
162.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-542-8
Beilstein/REAXYS Number:
637031
MDL number:
Assay:
96% (NT)
Form:
liquid
Servicio técnico
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Permítanos ayudarleQuality Level
assay
96% (NT)
form
liquid
color
APHA: ≤20
refractive index
n20/D 1.398
bp
93-94 °C/18 mmHg (lit.)
solubility
95% ethanol: 4.5 g/10 mL, clear, colorless
density
1.121 g/mL at 20 °C, 1.101 g/mL at 25 °C (lit.)
functional group
carbonate
shipped in
wet ice
storage temp.
2-8°C
SMILES string
CCOC(=O)OC(=O)OCC
InChI
1S/C6H10O5/c1-3-9-5(7)11-6(8)10-4-2/h3-4H2,1-2H3
InChI key
FFYPMLJYZAEMQB-UHFFFAOYSA-N
General description
Diethyl pyrocarbonate (DEP) is a bactericidal agent and decomposes in water to CO2 and ethanol. DEP inhibits enzymes such as DNase and RNase without affecting nucleic acids. It is useful for the preparation of mRNA from tissues.
Application
Reactivo de modificación para residuos de His y Tyr en proteínas. Sonda robusta para alteraciones estructurales en el ADN bicatenario, que reacciona con las bases total o parcialmente desapiladas.
Diethyl pyrocarbonate may be used in the following studies:
- For the modification of histidyl residues in proteins.
- As a nuclease inhibitor, for the extraction of undegraded nucleic acids from etiolated and green plant tissues.
- For the modification of linear and supercoiled plasmid DNAs.
- As a chemical probe to investigate the secondary structure in negatively supercoiled DNA.
- For cabethoxylation of histidine residues of actin.
Biochem/physiol Actions
Inactiva la ARNasa en disolución aproximadamente al 0,1% (v/v). Por tanto, protege el ARN contra la degradación.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Clase de almacenamiento
10 - Combustible liquids
wgk
WGK 3
flash_point_f
156.2 °F - closed cup
flash_point_c
69 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
W Herr
Proceedings of the National Academy of Sciences of the United States of America, 82(23), 8009-8013 (1985-12-01)
Purine residues located within regions of DNA that have the potential to form left-handed Z-helical structures are modified preferentially by diethyl pyrocarbonate; this hyperreactivity is dependent on the degree of negative superhelicity of the circular DNA molecules. As negative superhelical
Modification of histidyl residues in proteins by diethylpyrocarbonate.
E W Miles
Methods in enzymology, 47, 431-442 (1977-01-01)
Effects of diethyl pyrocarbonate and methyl methanesulfonate on nucleic acids and nucleases.
I Fedorcsák et al.
Acta chemica Scandinavica, 20(1), 107-112 (1966-01-01)
