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O-(TERT-BUTYLDIMETHYLSILYL)HYDROXYLAMINE

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O-(TERT-BUTYLDIMETHYLSILYL)HYDROXYLAMINE Basic information

Product Name:
O-(TERT-BUTYLDIMETHYLSILYL)HYDROXYLAMINE
Synonyms:
  • O-(TERT-BUTYLDIMETHYLSILYL)HYDROXYLAMINE
  • O-(T-BUTYLDIMETHYLSILYL)HYDROXYLAMINE
  • AMINOXY-TERT-BUTYLDIMETHYLSILANE
  • AKOS 91557
  • O-(tert-Butyldiemthylsilyl)hydroxylamine
  • OtertButyldiemthylsilylhydroxylamine
  • o-(tert-butyldimethylsilyl)hydroxylamine, 95
  • tert-Butyldimethylsilyloxyamine.
CAS:
41879-39-4
MF:
C6H17NOSi
MW:
147.29
Mol File:
41879-39-4.mol
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O-(TERT-BUTYLDIMETHYLSILYL)HYDROXYLAMINE Chemical Properties

Melting point:
62-65 °C (lit.)
Boiling point:
87-90 °C/40 mmHg (lit.)
Density 
0.849±0.06 g/cm3(Predicted)
Flash point:
54°C
storage temp. 
2-8°C
solubility 
freely sol hexane, chloroform, and most organic solvents; insol water.
pka
4.75±0.70(Predicted)
form 
solid
Appearance
Colorless to off-white Solid-Liquid Mixture
Water Solubility 
Hydrolyzes in water.
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
Sensitive 
Moisture Sensitive
BRN 
2424306
InChI
InChI=1S/C6H17NOSi/c1-6(2,3)9(4,5)8-7/h7H2,1-5H3
InChIKey
SSUCKKNRCOFUPT-UHFFFAOYSA-N
SMILES
NO[Si](C(C)(C)C)(C)C
CAS DataBase Reference
41879-39-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
UN 3259 8/PG 2
WGK Germany 
3
10-21
TSCA 
No
HazardClass 
8
PackingGroup 
III

MSDS

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O-(TERT-BUTYLDIMETHYLSILYL)HYDROXYLAMINE Usage And Synthesis

Physical properties

mp 62–65°C; bp 87–90°C/40 mmHg.

Uses

O-(tert-Butyldimethylsilyl)hydroxylamine (tert-butyldimethylsilyl-O-hydroxylamine)is used to induce the cleavage, during solid supported synthesis of hydroxamic acids. It also finds it uses as a chemical additive and an intermediate.

Uses

O-(tert-Butyldimethylsilyl)hydroxylamine (tert-butyldimethylsilyl-O-hydroxylamine) may be used to induce the cleavage, during solid supported synthesis of hydroxamic acids.

Preparation

the reagents are most conveniently prepared by treatment of hydroxylamine hydrochloride with ethylenediamine in dichloromethane, followed by the appropriate chlorosilane.A two-step procedure using ammonia in place of ethylenediamine has also been reported.

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