Skip to Content
Merck
CN

11514

Hydroxylamine hydrochloride

≥99.9995% (metals basis)

Synonym(s):

Hydroxylammonium chloride

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
NH2OH · HCl
CAS Number:
Molecular Weight:
69.49
EC Number:
226-798-2
UNSPSC Code:
41116105
PubChem Substance ID:
Beilstein/REAXYS Number:
3539763
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

WTDHULULXKLSOZ-UHFFFAOYSA-N

InChI

1S/ClH.H3NO/c;1-2/h1H;2H,1H2

SMILES string

Cl.NO

assay

≥99.9995% (metals basis)

form

solid

mp

155-157 °C (dec.) (lit.)

density

1.67 g/mL at 25 °C (lit.)

anion traces

sulfate (SO42-): ≤50 mg/kg

cation traces

Ag: ≤0.01 mg/kg, Al: ≤0.05 mg/kg, As: ≤0.005 mg/kg, Ba: ≤0.05 mg/kg, Be: ≤0.01 mg/kg, Bi: ≤0.01 mg/kg, Ca: ≤1 mg/kg, Cd: ≤0.01 mg/kg, Co: ≤0.01 mg/kg, Cr: ≤0.1 mg/kg, Cs: ≤0.01 mg/kg, Cu: ≤0.2 mg/kg, Fe: ≤0.5 mg/kg, Ga: ≤0.01 mg/kg, Hg: ≤0.001 mg/kg, In: ≤0.01 mg/kg, Ir: ≤0.01 mg/kg, K: ≤0.1 mg/kg, Li: ≤0.01 mg/kg, Mg: ≤0.2 mg/kg, Mn: ≤0.05 mg/kg, Mo: ≤0.01 mg/kg, Na: ≤1 mg/kg, Ni: ≤0.05 mg/kg, Os: ≤0.01 mg/kg, Pb: ≤0.01 mg/kg, Pd: ≤0.01 mg/kg, Pt: ≤0.1 mg/kg, Rb: ≤0.01 mg/kg, Rh: ≤0.01 mg/kg, Ru: ≤0.01 mg/kg, Sb: ≤0.01 mg/kg, Se: ≤0.01 mg/kg, Sn: ≤0.05 mg/kg, Sr: ≤0.01 mg/kg, Tl: ≤0.01 mg/kg, V: ≤0.01 mg/kg, Zn: ≤0.2 mg/kg

Looking for similar products? Visit Product Comparison Guide

Biochem/physiol Actions

MAO inhibitor; inhibits platelet aggregation.

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Carc. 2 - Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral

target_organs

spleen

Storage Class

4.1A - Other explosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Bereket Y Oquare et al.
Bioconjugate chemistry, 19(11), 2196-2204 (2008-10-04)
We report the design and synthesis of an orthogonally protected peptide nucleic acid (PNA) building block, Fmoc-PNA-U'-(Dde)-OH, and its use in the construction of PNA FRET probes. This building block allows for the post-synthetic attachment of reporter groups to the
Anke Bill et al.
PloS one, 9(6), e97973-e97973 (2014-06-03)
The human prostacyclin receptor (hIP receptor) is a seven-transmembrane G protein-coupled receptor (GPCR) that plays a critical role in vascular smooth muscle relaxation and platelet aggregation. hIP receptor dysfunction has been implicated in numerous cardiovascular abnormalities, including myocardial infarction, hypertension
Daniel F Dwyer et al.
Journal of immunology (Baltimore, Md. : 1950), 193(2), 529-539 (2014-06-15)
Papain, a cysteine protease allergen with inherent adjuvant activity, induces potent IL-4 expression by T cells in the popliteal lymph nodes of mice following footpad immunization. In this study, we identify a novel, non-BCR-mediated capacity for B cells to rapidly
Srikanth Pedireddy et al.
Nature communications, 5, 4947-4947 (2014-09-18)
Nanoporous gold with networks of interconnected ligaments and highly porous structure holds stimulating technological implications in fuel cell catalysis. Current syntheses of nanoporous gold mainly revolve around de-alloying approaches that are generally limited by stringent and harsh multistep protocols. Here
Ayman M Saleh et al.
Molecules (Basel, Switzerland), 19(9), 13076-13092 (2014-08-27)
A selected set of substituted pyridone-annelated isoindigos 3a-f has been synthesized via interaction of 5- and 6-substituted oxindoles 2a-f with 6-ethyl-1,2,9-trioxopyrrolo[3,2-f]quinoline-8-carboxylic acid (1) in acetic acid at reflux. Among these isoindigos, the 5'-chloro and 5'-bromo derivatives 3b and 3d show

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service