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O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE

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O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE Basic information

Product Name:
O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE
Synonyms:
  • O-(tert-Butyl)hydroxylamine hydrochloride 98%
  • O-T-BUTYLHYDROXYLAMINE HYDROCHLORIDE
  • O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE
  • O-Tert-ButylhydroxylamineHCl
  • 2-Aminooxy-2-methylpropane hydrochloride
  • O-(1,1-Dimethylethyl)hydroxylamine hydrochloride
  • tert-Butoxyamine hydrochloride
  • HydroxylaMine,O-(1,1-diMethylethyl)-, hydrochloride (1:1)
CAS:
39684-28-1
MF:
C4H12ClNO
MW:
125.6
EINECS:
254-590-1
Product Categories:
  • Building Blocks
  • Chemical Synthesis
  • Hydroxylamines
  • Nitrogen Compounds
  • Nitrogen Compounds
  • Organic Building Blocks
  • Organic Building Blocks
Mol File:
39684-28-1.mol
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O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE Chemical Properties

Melting point:
158-159 °C(lit.)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
H2O: soluble0.5g/10 mL
form 
powder to crystal
color 
White to Almost white
BRN 
3668106
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Safety Information

Hazard Codes 
F
Risk Statements 
11
RIDADR 
UN 1325 4.1/PG 3
WGK Germany 
3
10
HazardClass 
4.1
PackingGroup 
HS Code 
29280090

MSDS

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O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE Usage And Synthesis

Chemical Properties

White crystalline powder

Uses

Reactant involved in synthesis of biologically active molecules including:• ;CGS 25966 derivatives for use as MMP inhibitors1• ;Imidazolidinedione derivatives for use as antimalarial treatments2• ;Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists3• ;Rab proteins for isoprenylation and geranylgeranylation inhibition4Reactant involved in:• ;Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents5• ;Double allylic alkylation of indole-2-hydroxamates6• ;SN2 substitution reactions at amide nitrogens7• ;Photoc

Uses

O-tert-Butylhydroxylamine Hydrochloride is an reactant used in various synthesis of biologically active molecules such as camptothecin derivatives that exerts anti-tumor activity, oxime derivatives as GPR119 agonists and their preparation and highly Potent Matrix Metalloproteinase Inhibitors.

Uses

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

O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDESupplier

Suzhou Highfine Biotech Co., Ltd Gold
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0512-68417696 13962195629
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qirl@highfine.com
Zhengzhou Kingsfine Chemical Co., Ltd. Gold
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0371-56632527 13838252817
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sales@kingsfine.com
J & K SCIENTIFIC LTD.
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010-82848833 400-666-7788
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jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
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4006608290; 18621169109
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market03@meryer.com
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Email
Sales-CN@TCIchemicals.com