Skip to Content
Merck
CN

225185

Cyclobutylamine

98%

Synonym(s):

Aminocyclobutane

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
C4H7NH2
CAS Number:
Molecular Weight:
71.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-736-0
Beilstein/REAXYS Number:
2069297
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Cyclobutylamine, 98%

InChI key

KZZKOVLJUKWSKX-UHFFFAOYSA-N

InChI

1S/C4H9N/c5-4-2-1-3-4/h4H,1-3,5H2

SMILES string

NC1CCC1

assay

98%

form

liquid

refractive index

n20/D 1.437 (lit.)

bp

81.5 °C/752 mmHg (lit.)

density

0.833 g/mL at 25 °C (lit.)

storage temp.

2-8°C

Quality Level

Looking for similar products? Visit Product Comparison Guide

pictograms

FlameCorrosion

signalword

Danger

hcodes

Hazard Classifications

Flam. Liq. 2 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

24.8 °F - closed cup

flash_point_c

-4 °C - closed cup

ppe

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

Regulatory Information

危险化学品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

McNaughton et al.
Journal of molecular spectroscopy, 196(2), 274-282 (1999-11-30)
The infrared spectrum of vinylamine, generated by pyrolysis of cyclobutylamine, has been investigated at low and high resolution. The rovibrational structure of the far infrared spectrum (0.002 cm(-1)) has been analyzed, and effective rotational and centrifugal distortion constants have been
T Maruyama et al.
Chemical & pharmaceutical bulletin, 38(10), 2719-2725 (1990-10-01)
9-Cyclobutyladenine (4a), cis- and trans-9-[3- (hydroxymethyl)cyclobutyl]adenine (4b) and 9-[3,3-bis(hydroxymethyl)cyclobutyl]adenine(4d) were prepared from the corresponding cyclobutylamine derivatives (1a, 1b and 1d). Guanine congeners (9a, cis- and trans-9b and 9d) and carbocyclic oxetanocin G (1',2'-trans-9f) were also prepared. Carbocyclic oxetanocin A(1',2'-trans-4f), the
Hartmut Schirok
The Journal of organic chemistry, 71(15), 5538-5545 (2006-07-15)
7-Azaindoles are versatile building blocks, especially in medicinal chemistry, where they serve as bioisosteres of indoles or purines. Herein, we are presenting a robust and flexible synthesis of 1,3- and 1,3,6-substituted 7-azaindoles starting from nicotinic acid derivatives or 2,6-dichloropyridine, respectively.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service