Skip to Content
MilliporeSigma
All Photos(1)

Documents

479675

Sigma-Aldrich

N-(tert-Butyl)hydroxylamine acetate

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)3CNHOH·CH3CO2H
CAS Number:
Molecular Weight:
149.19
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

mp

65-69 °C (lit.)

SMILES string

CC(O)=O.CC(C)(C)NO

InChI

1S/C4H11NO.C2H4O2/c1-4(2,3)5-6;1-2(3)4/h5-6H,1-3H3;1H3,(H,3,4)

InChI key

QGYZLVSWEOXOFT-UHFFFAOYSA-N

Related Categories

General description

N-(tert-Butyl)hydroxylamine acetate (NtBuHA acetate) is a derivative of hydroxylamine that shows thioesterase-mimetic and antioxidant characteristics.

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:
  • (Z)-α-5-bromo-N-tert-butyl-2-methoxyphenylnitrone
  • ONO-type pincer ligand
  • hydroxyphenyl nitrones

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

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’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

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

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