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438227

Sigma-Aldrich

Hydroxylamine solution

50 wt. % in H2O

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Synonym(s):
HDA
Linear Formula:
NH2OH
CAS Number:
Molecular Weight:
33.03
EC Number:
MDL number:
PubChem Substance ID:

vapor pressure

9 mmHg ( 40 °C)

Quality Level

form

liquid

concentration

50 wt. % in H2O

bp

>100 °C

density

1.078 g/mL at 25 °C

SMILES string

NO

InChI

1S/H3NO/c1-2/h2H,1H2

InChI key

AVXURJPOCDRRFD-UHFFFAOYSA-N

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1 of 4

This Item
21497355460179728
Hydroxylamine solution 50 wt. % in H2O

Sigma-Aldrich

438227

Hydroxylamine solution

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

Sigma-Aldrich

55460

Hydroxylamine hydrochloride

Essential Grade
bp

>100 °C

bp

-

bp

-

bp

-

density

1.078 g/mL at 25 °C

density

1.23 g/mL at 25 °C

density

1.67 g/mL at 25 °C (lit.)

density

0.892 g/mL at 25 °C

vapor pressure

9 mmHg ( 40 °C)

vapor pressure

-

vapor pressure

0.001 hPa ( 50 °C)

vapor pressure

-

concentration

50 wt. % in H2O

concentration

1.0 M in methylene chloride

concentration

-

concentration

1.0 M lithium triethylborohydride in THF

Oxammonium, Azanol, H2NHO, dihydridohydroxidonitrogen, HOA, NH2OH, Hydroxylamine solution supplier, nitrogen cycle, nitrification, electrophiles, 1-Hexadecylamine, 1-hexadecanylamine, 1-Aminohexadecane, Cetylamine, n-Certylamine, 1-hexadecanamine, HAD, Alamine 6, Amine 16D, Armeen 16, Cetylamin, Crodamine, Palmitylamine, palmityl amine.

-

-

-

General description

Hydroxylamine is a weak base that is mainly used as a reducing agent in organic reactions.

Application

Reactant for preparation of:
  • Prodrug for cardiovascular agent Nω-hydroxy-L-arginine (NOHA, nitric oxide precursor)
  • Hydroxyaminoguanidines as anti-cancer agents
  • Nonsteroidal 2,3-dihydroquinoline glucocorticoid receptor agonists with reduced phosphoenolpyruvate caboxykinase (PEPCK) transactivation
  • Carboxamide derivatives of ofloxacin with improved antimicrobial properties
  • Analogues of coumarin based TNF-α converting enzyme (TACE) inhibitors
  • HIV integrase inhibitors

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Carc. 2 - Desen. Expl. 4 - Eye Dam. 1 - Met. Corr. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 - STOT SE 3

Target Organs

Blood, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Reducing graphene oxide via hydroxylamine: a simple and efficient route to graphene.
Zhou X, et al.
The Journal of Physical Chemistry C, 115(24), 11957-11961 (2011)
Elie Akanny et al.
Analytical and bioanalytical chemistry, 411(21), 5563-5576 (2019-06-19)
The Surface-enhanced Raman spectroscopy (SERS) method based on gold nanoparticles as SERS substrate was investigated for the label-free detection and quantification of probiotic bacteria that are widely used in various pharmaceutical formulations. Indeed, the development of a simple and fast
Ian R Kelsall et al.
Proceedings of the National Academy of Sciences of the United States of America, 116(27), 13293-13298 (2019-06-19)
The linear ubiquitin assembly complex (LUBAC) comprises 3 components: HOIP, HOIL-1, and Sharpin, of which HOIP and HOIL-1 are both members of the RBR subfamily of E3 ubiquitin ligases. HOIP catalyses the formation of Met1-linked ubiquitin oligomers (also called linear
Assembly of cyclic peptide dendrimers from unprotected linear building blocks in aqueous solution.
DavidaPallin T.
Chemical Communications (Cambridge, England), 11, 1345-1346 (1996)
A E Cribb et al.
Clinical pharmacology and therapeutics, 51(5), 522-526 (1992-05-01)
The oxidation of sulfamethoxazole to its hydroxylamine metabolite was investigated in vitro with human liver microsomes and in vivo by detection in the urine. Sulfamethoxazole was oxidized to the hydroxylamine in an NADPH-dependent process by liver microsomes prepared from two

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