96328
tert-Butylamine hydrochloride
≥98.0% (AT)
Synonym(s):
2-Amino-2-methylpropane hydrochloride
Sign Into View Organizational & Contract Pricing
All Photos(1)
Select a Size
Change View
100 G
$87.60
About This Item
Linear Formula:
(CH3)3CNH2 · HCl
CAS Number:
Molecular Weight:
109.60
Beilstein/REAXYS Number:
3905687
EC Number:
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
Quality Level
assay
≥98.0% (AT)
form
powder
impurities
<0.5% water
SMILES string
Cl.CC(C)(C)N
InChI
1S/C4H11N.ClH/c1-4(2,3)5;/h5H2,1-3H3;1H
InChI key
DLDIDQIZPBIVNQ-UHFFFAOYSA-N
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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
Sankar K Guchhait et al.
Organic & biomolecular chemistry, 8(16), 3631-3634 (2010-06-25)
With the development of a novel microwave-assisted one-pot tandem de-tert-butylation of tert-butyl amine in an Ugi-type multicomponent reaction product, tert-butyl isocyanide as a useful convertible isonitrile has been explored for the first time affording access to molecular diversity of pharmaceutically-important
Active Filters
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
