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Merck
CN

D5520

Dimethyl dicarbonate

for histidine methylation

Synonym(s):

DMPC, Dimethyl pyrocarbonate, Pyrocarbonic acid dimethyl ester

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About This Item

Linear Formula:
(CH3OCO)2O
CAS Number:
Molecular Weight:
134.09
EC Number:
224-859-8
UNSPSC Code:
12352202
PubChem Substance ID:
Beilstein/REAXYS Number:
956715
MDL number:
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InChI key

GZDFHIJNHHMENY-UHFFFAOYSA-N

InChI

1S/C4H6O5/c1-7-3(5)9-4(6)8-2/h1-2H3

SMILES string

COC(=O)OC(=O)OC

biological source

synthetic

form

liquid

refractive index

n20/D 1.392 (lit.)

bp

45-46 °C/5 mmHg (lit.)

density

1.25 g/mL at 25 °C (lit.)

storage temp.

room temp

Application

Methylates one or two histidine residues at the active site of PEP carboxykinase; the resulting inhibition is only partially reversible.

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

185.0 °F

flash_point_c

85 °C

ppe

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

Regulatory Information

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Small (Weinheim an der Bergstrasse, Germany), 12(44), 6106-6113 (2016-09-21)
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Scientific reports, 7(1), 4974-4974 (2017-07-12)
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Amanuel Wolde-Kidan et al.
Physical chemistry chemical physics : PCCP, 21(31), 16989-17000 (2019-07-26)
The influence of the co-solutes TMAO, urea, and NaCl on the hydration repulsion between lipid membranes is investigated in a combined experimental/simulation approach. Pressure-hydration curves obtained via sorption experiments reveal that the repulsion significantly increases when the membranes are loaded

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