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374148

N-tert-Butylisopropylamine

Name: <I>N</I>-<I>tert</I>-Butylisopropylamine
Brand: ALDRICH

97%

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About This Item

Linear Formula:

(CH₃)₃CNHCH(CH₃)₂

CAS Number:

7515-80-2

Molecular Weight:

115.22

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24863283

EC Number:

231-370-3

Beilstein/REAXYS Number:

1846752

MDL number:

MFCD00037059

Assay:

97%

Form:

liquid

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Properties

assay

97%

form

liquid

refractive index

n20/D 1.398 (lit.)

bp

98 °C (lit.)

density

0.727 g/mL at 25 °C (lit.)

functional group

amine

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

Description

General description

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

pictograms

GHS02,GHS05

signalword

Danger

hcodes

H226,H314

pcodes

P210 - P233 - P240 - P280 - P303 + P361 + P353 - P305 + P351 + P338

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

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

Regulatory Information

危险化学品

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Enamines from terminal epoxides and hindered lithium amides.

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

Global Trade Item Number

SKU	GTIN
374148-5G	04061836826635