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13-2291

Sigma-Aldrich

Hydroxylamine hydrochloride

≥97.0%, suitable for determination of toxic metals

Synonym(s):

Hydroxylammonium chloride

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About This Item

Linear Formula:
NH2OH · HCl
CAS Number:
Molecular Weight:
69.49
Beilstein:
3539763
EC Number:
MDL number:
UNSPSC Code:
12352301
PubChem Substance ID:

Assay

≥97.0%

form

crystalline

availability

available only in Japan

technique(s)

inhibition assay: suitable

pH

2.5-3.5 (20 °C, 50 g/L)

mp

155-157 °C (dec.) (lit.)

solubility

water: soluble

density

1.67 g/mL at 25 °C (lit.)

suitability

suitable for determination of toxic metals

SMILES string

Cl.NO

InChI

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

InChI key

WTDHULULXKLSOZ-UHFFFAOYSA-N

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Biochem/physiol Actions

MAO inhibitor; inhibits platelet aggregation.

Signal Word

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 Code

4.1A - Other explosive hazardous materials

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Journal of hazardous materials, 402, 123760-123760 (2020-12-02)
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Ayman M Atta et al.
International journal of molecular sciences, 16(4), 6911-6931 (2015-03-31)
In the present study, a new magnetic powder based on magnetite can be used as a petroleum crude oil collector. Amidoximes based on rosin as a natural product can be prepared from a reaction between hydroxylamine and rosin/acrylonitrile adducts. The
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PloS one, 9(6), e97973-e97973 (2014-06-03)
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Marte S Dragset et al.
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Efficient iron acquisition is crucial for the pathogenesis of Mycobacterium tuberculosis. Mycobacterial iron uptake and metabolism are therefore attractive targets for antitubercular drug development. Resistance mutations against a novel pyrazolopyrimidinone compound (PZP) that is active against M. tuberculosis have been

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