96328
tert-Butylamine hydrochloride
≥98.0% (AT)
Synonym(s):
2-Amino-2-methylpropane hydrochloride
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About This Item
Linear Formula:
(CH3)3CNH2 · HCl
CAS Number:
Molecular Weight:
109.60
UNSPSC Code:
41116105
NACRES:
NA.21
PubChem Substance ID:
EC Number:
233-009-5
Beilstein/REAXYS Number:
3905687
MDL number:
Product Name
tert-Butylamine hydrochloride, ≥98.0% (AT)
InChI
1S/C4H11N.ClH/c1-4(2,3)5;/h5H2,1-3H3;1H
InChI key
DLDIDQIZPBIVNQ-UHFFFAOYSA-N
SMILES string
Cl.CC(C)(C)N
assay
≥98.0% (AT)
form
powder
impurities
<0.5% water
Quality Level
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F Alvarado et al.
Biochimica et biophysica acta, 613(1), 140-152 (1980-01-01)
The activation of rabbit brush-border sucrase by the alkali metal ions, Li+, Na+ and K+, was analyzed using the equations of the random-order allosteric model previously proposed for sucrase (Mahmood, A. and Alvarado, F. (1975) Arch. Biochem. Biophys. 168, 585).
Marina Bicchieri et al.
Analytical and bioanalytical chemistry, 402(4), 1517-1528 (2011-07-14)
The Italian dialect poet Cesare Pascarella travelled all around the world, noting down in notebooks his keen and caustic observations, and drawing sketches that are a visual reportage of his journeys. The sketches were mounted as a random collage over
A R Ekkati et al.
Amino acids, 38(3), 747-751 (2009-04-01)
N-Acetyl-AA(amino acid)-NHtBu derivatives of all 20 naturally occurring amino acids have been synthesized. Syntheses were performed via solution-phase methodology with yields that allow for access to gram quantities of substrates, in most cases. Syntheses include the coupling of a hindered
Shunzo Yamamoto et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 70(2), 265-269 (2007-09-07)
The liquid-phase mercury-photosensitized luminescence of tert-butyl alcohol (TL)-tert-butylamine (TM) mixtures has been investigated by a steady-state illumination method over a wide range of substrate concentrations. The emission bands from exciplexes (HgTL* and HgTM*) between an excited mercury atom and an
Estimation, prevention, and quality control of carbon dioxide loss during aerobic sample processing.
Z L Bandi
Clinical chemistry, 27(10), 1676-1681 (1981-10-01)
We find that 2 to 6 mmol of carbon dioxide per liter (mean: 4.1 mmol/L) is lost during routine laboratory processing of patients' serum samples after centrifugation. Additional CO2 may be lost if evacuated blood-collection tubes are not filled completely
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