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Merck

96328

Sigma-Aldrich

tert-Butylamine hydrochloride

≥98.0% (AT)

Sinónimos:

2-Amino-2-methylpropane hydrochloride

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About This Item

Fórmula lineal:
(CH3)3CNH2 · HCl
Número de CAS:
Peso molecular:
109.60
Beilstein/REAXYS Number:
3905687
EC Number:
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NA.21

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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
Pinnelli S R Prasad et al.
The journal of physical chemistry. A, 113(24), 6540-6543 (2009-05-23)
The first proof-of-concept of the formation of a double tert-butylamine (t-BuNH(2)) + hydrogen (H(2)) clathrate hydrate has been demonstrated. Binary clathrate hydrates with different molar concentrations of the large guest t-BuNH(2) (0.98-9.31 mol %) were synthesized at 13.8 MPa and

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