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225185

Sigma-Aldrich

Cyclobutylamine

98%

Synonym(s):

Aminocyclobutane

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About This Item

Linear Formula:
C4H7NH2
CAS Number:
2516-34-9
Molecular Weight:
71.12
Beilstein:
2069297
EC Number:
219-736-0
MDL number:
MFCD00001328
UNSPSC Code:
12352100
PubChem Substance ID:
24853483
NACRES:
NA.22

Quality Level

100

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

SMILES string

NC1CCC1

InChI

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

InChI key

KZZKOVLJUKWSKX-UHFFFAOYSA-N

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Related Categories

Pictograms

FlameCorrosion
GHS02,GHS05

Signal Word

Danger

Hazard Statements

H225,H314

Hazard Classifications

Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

24.8 °F - closed cup

Flash Point(C)

-4 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

JAN Code

225185-BULK:
225185-5G:
225185-25G:
225185-1G:
225185-VAR:
225185-250MG:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM5933
MKCK3490
MKCF9135
MKCD9947
MKBX9526V

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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.

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