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Merck

254940

Sigma-Aldrich

Methyl acetimidate hydrochloride

technical grade

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25 G
MXP 12,939.00

MXP 12,939.00


Fecha estimada de envío17 de abril de 2025


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25 G
MXP 12,939.00

About This Item

Fórmula lineal:
CH3C(=NH)OCH3 · HCl
Número de CAS:
Peso molecular:
109.55
Beilstein/REAXYS Number:
3671581
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

MXP 12,939.00


Fecha estimada de envío17 de abril de 2025


Solicitar un pedido a granel

grade

technical grade

Quality Level

mp

105 °C (dec.) (lit.)

functional group

amine

storage temp.

2-8°C

SMILES string

Cl.COC(C)=N

InChI

1S/C3H7NO.ClH/c1-3(4)5-2;/h4H,1-2H3;1H

InChI key

WHYJXXISOUGFLJ-UHFFFAOYSA-N

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General description

Methyl acetimidate hydrochloride is an inhibitor of N-methylation of phosphatidylethanolamine[1]. It also prevents the stimulation of purified cardiac sarcolemmal vesicles Ca2+-pump activities[1].

Application

Methyl acetimidate hydrochloride has been used in pre-crystallization chemical modification of lysine residues[2].

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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C Donnet et al.
The Journal of membrane biology, 163(3), 217-224 (1998-06-17)
The calcium pump of plasma membranes catalyzes the hydrolysis of ATP and phosphoric esters like p-nitrophenyl phosphate (pNPP). The latter activity requires the presence of ATP and/or calmodulin, and Ca2+ [22, 25]. We have studied the effects of nucleotide-analogues and
J Armstrong et al.
The EMBO journal, 2(10), 1641-1646 (1983-01-01)
The major (gene VIII) coat protein of bacteriophage fd was radiolabelled by treating the virus with methyl[3H]acetimidate without causing any loss of infectivity. Complete amidination of lysine-8 in the amino acid sequence of the protein was achieved but little or
Michael R Shortreed et al.
Analytical chemistry, 78(18), 6398-6403 (2006-09-15)
A powerful approach to relative quantification by mass spectrometry is to employ labeling reagents that target specific functional groups in molecules of interest. A quantitative comparison of two or more samples may be readily accomplished by using a chemically identical
V Panagia et al.
Biochimica et biophysica acta, 856(2), 383-387 (1986-04-14)
Incubation of purified cardiac sarcolemmal vesicles (SL) in the presence of S-adenosyl-L-methionine, a methyl donor for the enzymatic N-methylation of phosphatidylethanolamine (PE), increased the Ca2+-stimulated ATPase and ATP-dependent Ca2+ accumulation activities. Quantitative analysis of the methylated phospholipids revealed that maximal
K C Flanders et al.
Biochemistry, 21(18), 4244-4251 (1982-08-31)
N epsilon-Acetimidoglucagon to be used for semisynthesis was prepared by reacting glucagon with methyl acetimidate hydrochloride at pH 10.2, favoring acetimidation of the sole epsilon-amino group. N epsilon-Acetimidoglucagon was isolated from the crude acetimidoglucagon mixture by anion-exchange chromatography at pH

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