The molarity of a 50% solution for Product 467804 would be 15.1M. This is calculated based on the fact that 1M is equivalent to 33.03 g in 1L
467804
Hydroxylamine solution
50 wt. % in H2O, 99.999%
Synonym(s):
HDA
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10 ML
CHF 55.80
50 ML
CHF 103.00
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10 ML
CHF 55.80
50 ML
CHF 103.00
About This Item
Linear Formula:
NH2OH
CAS Number:
Molecular Weight:
33.03
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
99.999%
concentration
50 wt. % in H2O
bp
107 °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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General description
Hydroxylamine solution is widely used as a reducing agent and antioxidant in organic synthesis, polymer industry and water treatment.[1]
Application
Hydroxylamine solution (NH2OH) can be used as a reactant for the preparation of:
- Primary amides from aldehydes catalyzed by an arene–ruthenium(II) complex.[2]
- Hydroxyaminoguanidines and carboxamide derivatives of ofloxacin for biological studies.[3][4]
- Fe3O4/Au (GoldMag) nanoparticles for antibody immobilization.[5]
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 Statements
Precautionary Statements
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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Flutamide (2-methyl-N-[4-nitro-3-(trifluoromethyl)phenyl]-propanamide), a nonsteroidal antiandrogen, is used in the treatment of prostate cancer but is occasionally associated with hepatic dysfunction. In the present study, the metabolism of flutamide including the formation of the possible reactive toxic metabolites was investigated using
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