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358991

Sigma-Aldrich

N-tert-Butylmethylamine

97%

Synonym(s):

N-Methyl-tert-butylamine

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About This Item

Linear Formula:
(CH3)3CNHCH3
CAS Number:
14610-37-8
Molecular Weight:
87.16
Beilstein/REAXYS Number:
1730941
EC Number:
238-646-2
MDL number:
MFCD00042853
UNSPSC Code:
12352100
PubChem Substance ID:
24862045
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.395 (lit.)

bp

67-69 °C (lit.)

density

0.727 g/mL at 25 °C (lit.)

SMILES string

CNC(C)(C)C

InChI

1S/C5H13N/c1-5(2,3)6-4/h6H,1-4H3

InChI key

ZQGJEUVBUVKZKS-UHFFFAOYSA-N

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Application

N-tert-Butylmethylamine may be used in the preparation of 3-benzyl-N-tert-butyl-N,3-dimethyl-2,3-dihydrobenzofuran-6-carboxamide. N-tert-Butylmethylamine (N-Methyl-tert-butylamine) may be used in the preparation of 2-(α-N-methyl-tert-butylaminobenzyl)-1-indenone.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

-14.8 °F - closed cup

flash_point_c

-26 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mobile keto allyl systems. XVI. Thermal decomposition of 2-(. alpha.-N-methyl-tert-butylaminobenzyl)-1-indenone. Deamination-rearrangement.
Murray RJ and Cromwell NH.
The Journal of Organic Chemistry, 39(26), 3939-3941 (1974)
Philippe Diaz et al.
ChemMedChem, 4(10), 1615-1629 (2009-07-29)
We recently discovered and reported a series of N-alkyl-isatin acylhydrazone derivatives that are potent cannabinoid receptor 2 (CB(2)) agonists. In an effort to improve the druglike properties of these compounds and to better understand and improve the treatment of neuropathic
Karolina Klesiewicz et al.
The Journal of antibiotics, 69(11), 825-834 (2016-03-31)
A series of 20 xanthone derivatives was synthesized and evaluated for anti-Helicobacter pylori (H. pylori) activity. Qualitative and quantitative in vitro tests using the Kirby-Bauer method (agar disc-diffusion method) were performed. The tested compounds were screened against clarithromycin- and/or metronidazole-resistant

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