O-(tert-Butyl)hydroxylamine hydrochloride

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Names

[ CAS No. ]:
39684-28-1

[ Name ]:
O-(tert-Butyl)hydroxylamine hydrochloride

[Synonym ]:
tert-Butoxyamine Hydrochloride
MFCD00043272
Propane, 2-(aminooxy)-2-methyl-, hydrochloride (1:1)
O-tert-butylhydroxylamine,hydrochloride
EINECS 254-590-1
O-(tert-Butyl)hydroxylamine Hydrochloride
2-(Aminooxy)-2-methylpropane hydrochloride (1:1)
O-tert-ButylhydroxylamineHydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
110ºC at 760mmHg

[ Melting Point ]:
158-159ºC(lit.)

[ Molecular Formula ]:
C4H12ClNO

[ Molecular Weight ]:
125.597

[ Flash Point ]:
17.5ºC

[ Exact Mass ]:
125.060745

[ PSA ]:
35.25000

[ LogP ]:
2.17750

[ Water Solubility ]:
H2O: soluble0.5g/10 mL

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H228

[ Precautionary Statements ]:
P210

[ Personal Protective Equipment ]:
Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
F

[ Risk Phrases ]:
R11

[ RIDADR ]:
UN 1325 4.1/PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
Ⅲ

[ HS Code ]:
2922199090

Precursor & DownStream

Precursor

  • N-(tert-butoxy)phthalimide

DownStream

  • Methyl 2-fluorophenylglyoxylate O-tert-butyloxime
  • Methyl 3-fluorobenzoate
  • Gimatecan
  • ethyl 3-[(2-methylpropan-2-yl)oxyamino]-3-oxopropanoate

Customs

[ HS Code ]: 2922199090

[ Summary ]:
2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Synthesis and preliminary biological evaluation of new radioiodinated MMP inhibitors for imaging MMP activity in vivo.

Nucl. Med. Biol. 31(2) , 257-267, (2004)

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, rad...

T. Kolasa, A. Chimiak

Tetrahedron 30 , 3591, (1974)


More Articles

Related Compounds

  • O-ACETYL-N-(TERT-BUTYL)HYDROXYLAMINE HYDROCHLORIDE
  • n-(tert-butyl)hydroxylamine hydrochloride
  • N-tert-butyl-N-(1-diethoxyphosphoryl-2,2-dimethylpropyl)-O-(tert-butyl)hydroxylamine
  • O-tert-Butyl-L-serine methylester hydrochloride
  • O-tert-butyl-N-(4-methylbenzyl)hydroxylamine
  • O-tert-Butyl-L-threonine methyl ester hydrochloride
  • 5-[[4-(1-Phenylethyl)phenoxy]methyl]-4,5-dihydro-1,3-oxazol-2-amine
  • 2-(4-Tert-butylphenyl)-1-benzothiophen-6-ol
  • tert-butyl 3-(1H-pyrazol-1-yl)propanoate
  • 5-(2-ethoxycarbonyl-vinyl)-3-methyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester
  • (2R)-2-{[(tert-butoxy)carbonyl]amino}-3-methanesulfonylpropanoic acid
  • 4-(4-Aminomethyl-benzyl)-piperidine-1-carboxylic acid tert-butyl ester
  • (S)-3-(3-Bromo-[1,2,4]oxadiazol-5-yl)-piperidine-1-carboxylic acid tert-butyl ester
  • Tert-butyl 3-(3-bromo-1,2,4-oxadiazol-5-YL)piperidine-1-carboxylate
  • 3-Bromo-2-chlorobenzoic acid hydrazide
  • 1-(5-Fluoro-2-methylphenyl)but-3-en-1-amine
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