Hydroxylamine hydrochloride, ReagentPlus®, 99% | NH2OH · HCl

Properties

Related Categories	Bioactive Small Molecules, Biochemicals and Reagents, Cell Biology, Cell Signaling and Neuroscience, Enzyme Inhibitors, Enzyme Inhibitors by Enzyme, Enzymes, Inhibitors, and Substrates, Essential Chemicals, H, Inorganic Salts, Solutions and Reagents, Monoamine Oxidase, Neuroscience, Neurotransmission, Neurotransmitter Metabolism, P to Q, Peroxidase Inhibitors, Reagent Plus, Research Essentials More...
Quality Level	PREMIUM
grade	ReagentPlus^®
assay	99%
mp	155-157 °C (dec.)(lit.)
density	1.67 g/mL at 25 °C(lit.)

Description

Biochem/physiol Actions

MAO inhibitor; inhibits platelet aggregation.

Packaging

100, 500 g in poly bottle

3 kg in poly drum

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Price and Availability

Related Papers

Synthesis of peptide nucleic acid FRET probes via an orthogonally protected building block for post-synthetic labeling of peptide nucleic acids at the 5-position of uracil. Bereket Y. Oquare et al Bioconjug. Chem. 19, 2196-204, (2009)

Documents

Certificate of Analysis

Certificate of Origin

Safety Information

Symbol	GHS05, GHS07, GHS08, GHS09
Signal word	Warning
Hazard statements	H290-H302-H312-H315-H317-H319-H351-H373-H400
Precautionary statements	P273-P280-P305 + P351 + P338
Personal Protective Equipment	Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
Hazard Codes (Europe)	E,Xn,N
Risk Statements (Europe)	2-21/22-36/38-40-43-48/22-50
Safety Statements (Europe)	36/37-61
RIDADR	UN 2923 8/PG 2
WGK Germany	3
RTECS	NC3675000

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Papers

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Synthesis of peptide nucleic acid FRET probes via an orthogonally protected building block for post-synthetic labeling of peptide nucleic acids at the 5-position of uracil. Bereket Y. Oquare et al Bioconjug. Chem. 19, 2196-204, (2009)

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Chemical genetics reveals a complex functional ground state of neural stem cells Diamandis, P., et. al. Nat. Chem. Biol. 3(5), 268-273, (2007)

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Genetic mapping of targets mediating differential chemical phenotypes in Plasmodium falciparum. Jing Yuan et al Nat. Chem. Biol. 5, 765-71, (2009)

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Purification, characterization, and crystallization of monoamine oxidase from Escherichia coli K-12. Roh, J.H. Biosci. Biotechnol. Biochem. 58, 1652, (1994)

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Merck 14,4828

Fieser 1,478 / Fieser 2,217 / Fieser 7,176 / Fieser 9,245 / Fieser 11,257 / Fieser 15,170

Aldrich MSDS 1, 1062:A / Corp MSDS 1 (1), 1930:A / FT-IR 2 (3), 4713:A / FT-IR 1 (2), 1229:A / FT-IR 1 (2), 1227:D / IR-Spectra (2), 149:C / IR-Spectra (3), 165:C / RegBook 1 (3), 3203:B / Sax 6, 1576 / Sigma FT-IR 1 (2), 1025:C / Structure Index 1, 509:D:4

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Hydroxylamine hydrochloride

ReagentPlus^®, 99%

Properties

Description

Biochem/physiol Actions

Packaging

Legal Information

Price and Availability

Related Papers

Documents

Safety Information

Papers

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