Hydroxylamine hydrochloride

• Catalog No.: 379921
• CAS Number: 5470-11-1
• M. F.: ClH4NO
• M. W.: 69.49086
• Purity: 99.9999% trace metals basis

SYNONYMS

• Title: 羟胺 盐酸盐
• IUPAC name: hydroxylamine hydrochloride
• IUPAC Traditional name: hydroxylamine hydrochloride
• Synonyms: Hydroxylammonium chloride; 盐酸羟胺

DATABASE IDS

• EC Number: 226-798-2
• CAS Number: 5470-11-1
• PubChem SID: 24863700
• MDL Number: MFCD00051089
• Beilstein Number: 3539763

PROPERTIES

• Linear Formula: NH2OH · HCl
• Purity: 99.9999% trace metals basis
• Density: 1.67 g/mL at 25 °C(lit.)
• Melting Point: 155-157 °C (dec.)(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H290-H302-H312-H315-H317-H319-H351-H373-H400
• European Hazard Symbols: Explosive (E)
• European Hazard Symbols: Harmful (Xn)
• European Hazard Symbols: Nature polluting (N)
• 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
• GHS Precautionary statements: P273-P280-P305 + P351 + P338
• RID/ADR: UN 2923 8/PG 2
• Risk Statements: 2-21/22-36/38-40-43-48/22-50
• RTECS: NC3675000
• Safety Statements: 36/37-61
• Hazard Class: 8
• UN Number: 2923
• Packing Group: 2
• German water hazard class: 3

DETAILS

Description (English)

Biochem/physiol Actions
MAO inhibitor; inhibits platelet aggregation.
Packaging
5, 25 g in poly bottle
Application
Reactant for preparation of:
• Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel1
• Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents2
• Azapeptide tocolytic agents as inhibitors of prostaglandin F2α receptor for preventing preterm labor3
• Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B4
• Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys5545
• Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents6
• Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection7
• Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence8

Description (简体中文)

Biochem/physiol Actions
MAO 抑制剂;抑制血小板聚集。
包装
5, 25 g in poly bottle
Application
Reactant for preparation of:
• Organosilane amines as potent inhibitors and structural probes of influenza A virus M2 proton channel1
• Lamellarin D analogues as inibitors of topoisomerase I and potential antitumor agents2
• Azapeptide tocolytic agents as inhibitors of prostaglandin F2α receptor for preventing preterm labor3
• Thiazolidinones spiro-fused to indolin-2-ones as potent and selective inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B4
• Orally bioavailable quinoline-based antidiabetic dipeptidyl peptidase IV inhibitors targeting Lys5545
• Pyrimidine nucleoside derivatives with nitric oxide donors as antiviral agents6
• Benzyladenosine compounds targeting adenosine A2A receptor and adenosine transporter for neuroprotection7
• Naphthol derivatives as inhibitors of the vanilloid receptor TRPV1 with improved potency in rat cystometry models of urinary incontinence8