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Merck

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:
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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



pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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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
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