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Key Documents

274992

Sigma-Aldrich

O-Ethylhydroxylamine hydrochloride

97%

Synonym(s):

Ethoxyamine hydrochloride

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About This Item

Linear Formula:
CH3CH2ONH2 · HCl
CAS Number:
Molecular Weight:
97.54
Beilstein:
3606639
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

130-133 °C (lit.)

SMILES string

Cl[H].CCON

InChI

1S/C2H7NO.ClH/c1-2-4-3;/h2-3H2,1H3;1H

InChI key

NUXCOKIYARRTDC-UHFFFAOYSA-N

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Application

O-Ethylhydroxylamine hydrochloride was used in the determination of α-hydroxycarbonyl compounds.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Formation of α-hydroxycarbonyl and α-dicarbonyl compounds during degradation of monosaccharides.
NOVOtNy O, et al.
Czech Journal of Food Sciences, 25(3), 119-130 (2007)
Bo He et al.
Nature communications, 12(1), 4249-4249 (2021-07-14)
5-Hydroxymethylcytosine (5hmC) is an important epigenetic mark that regulates gene expression. Charting the landscape of 5hmC in human tissues is fundamental to understanding its regulatory functions. Here, we systematically profiled the whole-genome 5hmC landscape at single-base resolution for 19 types
Yafen Wang et al.
Chemical science, 10(2), 447-452 (2019-02-13)
5-Hydroxymethylcytosine (5hmC) is known as one of the vital players in nuclear reprogramming and the process of active DNA demethylation. Although the development of whole-genome sequencing methods for modified cytosine bases has burgeoned, the easily operated gene-specific loci detection of
Teresa Mairinger et al.
Analytical chemistry, 87(23), 11792-11802 (2015-10-30)
For the first time an analytical work flow based on accurate mass gas chromatography-quadrupole time-of-flight mass spectrometry (GC-QTOFMS) with chemical ionization for analysis providing a comprehensive picture of (13)C distribution along the primary metabolism is elaborated. The method provides a
Enkhtuul Tsogtbaatar et al.
Journal of experimental botany, 66(14), 4267-4277 (2015-02-26)
Pennycress (Thlaspi arvense L.), a plant naturalized to North America, accumulates high levels of erucic acid in its seeds, which makes it a promising biodiesel and industrial crop. The main carbon sinks in pennycress embryos were found to be proteins

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