479675
N-(tert-Butyl)hydroxylamine acetate
97%
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About This Item
Linear Formula:
(CH3)3CNHOH·CH3CO2H
CAS Number:
Molecular Weight:
149.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Product Name
N-(tert-Butyl)hydroxylamine acetate, 97%
InChI
1S/C4H11NO.C2H4O2/c1-4(2,3)5-6;1-2(3)4/h5-6H,1-3H3;1H3,(H,3,4)
SMILES string
CC(O)=O.CC(C)(C)NO
InChI key
QGYZLVSWEOXOFT-UHFFFAOYSA-N
assay
97%
mp
65-69 °C (lit.)
functional group
amine
carboxylic acid
Quality Level
Related Categories
Application
N-(tert-Butyl)hydroxylamine acetate has been used in a study to understand its effect on CD (cathepsin D) activity.
It may be used in the preparation of:
It may be used in the preparation of:
- (Z)-α-5-bromo-N-tert-butyl-2-methoxyphenylnitrone
- ONO-type pincer ligand
- hydroxyphenyl nitrones
General description
N-(tert-Butyl)hydroxylamine acetate (NtBuHA acetate) is a derivative of hydroxylamine that shows thioesterase-mimetic and antioxidant characteristics.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Microwave-assisted synthesis of hydroxyphenyl nitrones with protective action against oxidative stress.
Chavarria C, et al.
European Journal of Medicinal Chemistry, 58, 44-49 (2012)
(Z)-α-5-Bromo-N-tert-butyl-2-methoxyphenylnitrone.
Guo H, et al.
Acta Crystallographica Section E, Structure Reports Online, 63(10), 3943-3943 (2007)
Ruthenium ONO-Type Pincer Complex: Synthesis, Structural Characterization, and Catalysis.
Zhang Y, et al.
Advanced Synthesis & Catalysis, 352(10), 1779-1783 (2010)
Goutam Chandra et al.
Human molecular genetics, 24(19), 5416-5432 (2015-07-15)
Neurodegeneration is a devastating manifestation in the majority of >50 lysosomal storage disorders (LSDs). Neuronal ceroid lipofuscinoses (NCLs) are the most common childhood neurodegenerative LSDs. Mutations in 13 different genes (called CLNs) underlie various types of NCLs, of which the
Chinmoy Sarkar et al.
Journal of inherited metabolic disease, 43(5), 1082-1101 (2020-04-13)
Infantile neuronal ceroid lipofuscinosis (INCL) is a devastating neurodegenerative lysosomal storage disease (LSD) caused by inactivating mutations in the CLN1 gene. CLN1 encodes palmitoyl-protein thioesterase-1 (PPT1), a lysosomal enzyme that catalyzes the deacylation of S-palmitoylated proteins to facilitate their degradation
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