Hydroxylamine hydrochloride, puriss. p.a., ACS reagent, ≥99.0% (RT) | NH2OH · HCl

Properties

Related Categories	Analytical Reagents, Analytical Reagents for General Use, Analytical/Chromatography, Bioactive Small Molecules, Cell Biology, E-L, Puriss p.a. ACS, H, Puriss p.a. ACS More...
Quality Level	PREMIUM
grade	ACS reagent
	puriss. p.a.
assay	≥99.0% (RT)
ign. residue	≤0.05% (as SO₄)
pH	2.5-3.5 (25 °C, 50 mg/mL in H₂O)
mp	155-157 °C (dec.)(lit.)
density	1.67 g/mL at 25 °C(lit.)
anion traces	sulfate (SO₄^2-): ≤50 mg/kg
cation traces	Ca: ≤10 mg/kg
	Cd: ≤5 mg/kg
	Co: ≤5 mg/kg
	Cr: ≤5 mg/kg
	Cu: ≤5 mg/kg
	Fe: ≤5 mg/kg
	K: ≤50 mg/kg
	Mg: ≤5 mg/kg
	Mn: ≤5 mg/kg
	Na: ≤50 mg/kg
	Ni: ≤5 mg/kg
	Pb: ≤5 mg/kg
	Zn: ≤5 mg/kg

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Description

Biochem/physiol Actions

MAO inhibitor; inhibits platelet aggregation.

Price and Availability

Suggested Laboratory Gloves

This substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.

for splash & immersion protection

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

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

puriss. p.a., ACS reagent, ≥99.0% (RT)

Properties

Description

Biochem/physiol Actions

Price and Availability

Suggested Laboratory Gloves

Related Papers

Documents

Safety Information

Papers

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