96328
tert-Butylamine hydrochloride
≥98.0% (AT)
Synonym(s):
2-Amino-2-methylpropane hydrochloride
Sign In to View Organizational & Contract Pricing.
Select a Size
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Kana Sadaoka et al.
Bioorganic & medicinal chemistry, 19(13), 3901-3905 (2011-06-15)
Reduction of the 7-formyl groups in chlorophyll (Chl) b and its demetalated compound pheophytin (Phe) b was kinetically analyzed by using tert-butylamine-borane complex (t-BuNH(2)·BH(3)), and was compared with that of the 3-formyl groups in Chl d and Phe d. Reduction
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
M S Suleiman et al.
Journal of pharmaceutical and biomedical analysis, 8(4), 321-327 (1990-01-01)
A new salt of ibuprofen was prepared by reaction with t-butylamine; its formation was confirmed by IR and 1H-NMR spectroscopy. The salt was characterized by thermoanalytical, X-ray powder diffraction and solubility studies. The salt was found to be 1.5 times
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service