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O-tert-Butylhydroxylamine hydrochloride

ALDRICH/20023 - ≥99.0% (AT)

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

CAS Number: 39684-28-1
Empirical Formula (Hill Notation): C4H11NO · HCl
Molecular Weight: 125.60
EC Number: 254-590-1
MDL Number: MFCD00043272
Linear Formula: (CH3)3CONH2 · HCl
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-20023-1G 1 g
$65.60
1/EA
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45-20023-5G 5 g
$311.00
1/EA
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assay ≥99.0% (AT)
form solid
InChI 1S/C4H11NO.ClH/c1-4(2,3)6-5;/h5H2,1-3H3;1H
InChI key ZBDXGNXNXXPKJI-UHFFFAOYSA-N
mp ~155 °C (dec.)
Quality Level 200 
SMILES string Cl.CC(C)(C)ON
solubility H2O: soluble 0.5 g/10 mL
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.
Application: 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
Packaging: 1, 5 g in glass bottle
Symbol GHS02  GHS02
Signal word Warning
Hazard statements H228
Precautionary statements P210
Hazard Codes F
Risk Statements 11
RIDADR UN1325 - class 4.1 - PG 3 - Flammable solids, organic, n.o.s., H
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥99.0% (AT)
mp ~155 °C (dec.)
UNSPSC 12352100

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