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Merck
모든 사진(1)

주요 문서

96328

Sigma-Aldrich

tert-Butylamine hydrochloride

≥98.0% (AT)

동의어(들):

2-Amino-2-methylpropane hydrochloride

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About This Item

Linear Formula:
(CH3)3CNH2 · HCl
CAS Number:
Molecular Weight:
109.60
Beilstein:
3905687
EC Number:
MDL number:
UNSPSC 코드:
41116105
PubChem Substance ID:
NACRES:
NA.21

Quality Level

분석

≥98.0% (AT)

형태

powder

불순물

<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

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

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
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
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

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