Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

C99604

Sigma-Aldrich

Cycloheptylamine

99%

Synonym(s):

Aminocycloheptane

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C7H13NH2
CAS Number:
5452-35-7
Molecular Weight:
113.20
Beilstein:
1847543
EC Number:
226-693-1
MDL number:
MFCD00004153
UNSPSC Code:
12352100
PubChem Substance ID:
24893208
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.472 (lit.)

bp

54 °C/11 mmHg (lit.)

density

0.889 g/mL at 25 °C (lit.)

SMILES string

NC1CCCCCC1

InChI

1S/C7H15N/c8-7-5-3-1-2-4-6-7/h7H,1-6,8H2

InChI key

VXVVUHQULXCUPF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

107.6 °F

Flash Point(C)

42 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBK6731
STBK5954
STBB2739V
STBC5618V
STBC0558V

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Neelu Kaila et al.
Bioorganic & medicinal chemistry, 15(19), 6425-6442 (2007-08-01)
We have previously reported the discovery and initial SAR of the [1,7]naphthyridine-3-carbonitriles and quinoline-3-carbonitriles as Tumor Progression Loci-2 (Tpl2) kinase inhibitors. In this paper, we report new SAR efforts which have led to the identification of 4-alkylamino-[1,7]naphthyridine-3-carbonitriles. These compounds show
Julia Greiser et al.
Dalton transactions (Cambridge, England : 2003), 47(27), 9000-9007 (2018-06-21)
We report the isolation of a new type of 1,4-diazepan-6-amine (DAZA)-based ligand. Condensation of aldehydes with DAZA gives a novel class of 1,5-diazabicyclo[3.2.1]octanes in nearly quantitative yields. Subsequent reductive cleavage of these bicyclic aminal species with sodium borohydride selectively leads
Stelios Eleftheratos et al.
Bioorganic & medicinal chemistry letters, 20(14), 4182-4187 (2010-06-24)
Interaction of aminoadamantanes with the influenza A virus M2 proton channel was analyzed by docking simulations of a series of synthetic aminoadamantane derivatives, of differing binding affinity, into the crystal structure of the transmembrane (M2TM) pore. The pore blocking model
Oxygen-18 studies on the oxidative deamination mechanism of alicyclic primary amines in rabbit liver microsomes.
H Kurebayashi et al.
Archives of biochemistry and biophysics, 215(2), 433-443 (1982-05-01)
Tsung-Chi Chen et al.
Rapid communications in mass spectrometry : RCM, 25(21), 3274-3280 (2011-10-19)
The discontinuous atmospheric pressure interface (DAPI) has been developed to allow a direct transfer of ions from atmosphere into an ion trap mass spectrometer with minimum pumping capability. Air is introduced into the trap with ions and used as a

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