Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

179604

Sigma-Aldrich

exo-2-Aminonorbornane

99%

Synonym(s):

exo-2-Norbornanamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C7H13N
CAS Number:
7242-92-4
Molecular Weight:
111.18
EC Number:
230-647-6
MDL number:
MFCD00078132
UNSPSC Code:
12352100
PubChem Substance ID:
24850821
NACRES:
NA.22
Product 179604 is not currently sold in your country. Contact Technical Service

assay

99%

form

liquid

refractive index

n20/D 1.4807 (lit.)

bp

49 °C/10 mmHg (lit.)

density

0.938 g/mL at 25 °C (lit.)

SMILES string

N[C@@H]1C[C@H]2CC[C@@H]1C2

InChI

1S/C7H13N/c8-7-4-5-1-2-6(7)3-5/h5-7H,1-4,8H2/t5-,6+,7+/m0/s1

InChI key

JEPPYVOSGKWVSJ-RRKCRQDMSA-N

General description

exo-2-Aminonorbornane is an inhibitor of putrescine N-methyltransferase[1]. The structural and conformational properties of exo-2-aminonorbornane was studied[2].

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

95.0 °F - closed cup

flash_point_c

35 °C - closed cup

ppe

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BGBB0243V
BGBB0243
03306PH
91065JD
09710HD

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

Patricia Écija et al.
The Journal of chemical physics, 134(16), 164311-164311 (2011-05-03)
The intrinsic conformational and structural properties of the bicycle exo-2-aminonorbornane have been probed in a supersonic jet expansion using Fourier-transform microwave (FT-MW) spectroscopy and quantum chemical calculations. The rotational spectrum revealed two different conformers arising from the internal rotation of
N Hibi et al.
Plant physiology, 100(2), 826-835 (1992-10-01)
Biosynthesis of tropane alkaloids is thought to proceed by way of the diamine putrescine, followed by its methylation by putrescine N-methyltransferase (PMT; EC 2.1.1.53). High PMT activities were found in branch roots and/or cultured roots of several solanaceous plants. PMT

Questions

Reviews

No rating value

Active Filters

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