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Sigma-Aldrich

N-tert-Butylisopropylamine

97%

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About This Item

Linear Formula:
(CH3)3CNHCH(CH3)2
CAS Number:
7515-80-2
Molecular Weight:
115.22
Beilstein/REAXYS Number:
1846752
EC Number:
231-370-3
MDL number:
MFCD00037059
UNSPSC Code:
12352100
PubChem Substance ID:
24863283
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.398 (lit.)

bp

98 °C (lit.)

density

0.727 g/mL at 25 °C (lit.)

SMILES string

CC(C)NC(C)(C)C

InChI

1S/C7H17N/c1-6(2)8-7(3,4)5/h6,8H,1-5H3

InChI key

ZWXQPERWRDHCMZ-UHFFFAOYSA-N

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General description

N-tert-Butylisopropylamine participates in the synthesis of hindered enamines.

accessory

Product No.
Description
Pricing

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H314

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

77.0 °F - closed cup

flash_point_c

25 °C - closed cup

ppe

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

Certificates of Analysis (COA)

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David M Hodgson et al.
Journal of the American Chemical Society, 126(22), 6870-6871 (2004-06-04)
A new reactivity mode of lithium amides with epoxides leads to hindered enamines. The reaction of some of these enamines with unactivated primary and secondary alkyl halides is described, which expands the range of electrophiles that one can use in

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