Skip to Content
Merck
CN

20023

O-tert-Butylhydroxylamine hydrochloride

≥99.0% (AT)

Synonym(s):

2-Aminooxy-2-methylpropane hydrochloride, O-(1,1-Dimethylethyl)hydroxylamine hydrochloride, tert-Butoxyamine hydrochloride

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
(CH3)3CONH2 · HCl
CAS Number:
39684-28-1
Molecular Weight:
125.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57647770
EC Number:
254-590-1
Beilstein/REAXYS Number:
3668106
MDL number:
MFCD00043272

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

O-tert-Butylhydroxylamine hydrochloride, ≥99.0% (AT)

InChI key

ZBDXGNXNXXPKJI-UHFFFAOYSA-N

InChI

1S/C4H11NO.ClH/c1-4(2,3)6-5;/h5H2,1-3H3;1H

SMILES string

Cl.CC(C)(C)ON

assay

≥99.0% (AT)

form

solid

mp

~155 °C (dec.)

solubility

H2O: soluble 0.5 g/10 mL

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

O-tert-Butylhydroxylamine hydrochloride was used in the synthesis of N-methyl-O-tert-butylhydroxylamine hydrochloride. It was also used in the preparation of N-tert-butoxyamino acids as substrates for the unambiguous synthesis of N-hydroxy peptides.
Reactant involved in synthesis of biologically active molecules including:
  • CGS 25966 derivatives for use as MMP inhibitors
  • Imidazolidinedione derivatives for use as antimalarial treatments
  • Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists
  • Rab proteins for isoprenylation and geranylgeranylation inhibition

Reactant involved in:
  • Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents
  • Double allylic alkylation of indole-2-hydroxamates
  • SN2 substitution reactions at amide nitrogens
  • Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines

pictograms

Flame
GHS02

signalword

Warning

hcodes

H228

pcodes

P210

Hazard Classifications

Flam. Sol. 2

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCH4806
BCBG5972V
BCBJ2009V
1393448V
1393448

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Klaus Kopka et al.
Nuclear medicine and biology, 31(2), 257-267 (2004-03-12)
Non-invasive measurement of matrix metalloproteinase (MMP) activity in vivo is a clinical challenge in many disease processes such as inflammation, tumor metastasis and atherosclerosis. Therefore, radioiodinated analogues of the non-peptidyl broad-spectrum MMP inhibitor (MMPI) CGS 27023A 1a were synthesized for
T. Kolasa et al.
Tetrahedron, 30, 3591-3591 (1974)

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