Skip to Content
Merck
CN

391654

(1R,2R,3R,5S)-(−)-Isopinocampheylamine

95%

Synonym(s):

(−)-Isopinocampheylamine, (1R,2R,3R,5S)-3-Pinanamine

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C10H19N
CAS Number:
69460-11-3
Molecular Weight:
153.26
NACRES:
NA.22
PubChem Substance ID:
24864394
UNSPSC Code:
12352116
MDL number:
MFCD00192238
Assay:
95%
Form:
liquid

Key Documents

View All Documentation
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

InChI

1S/C10H19N/c1-6-8-4-7(5-9(6)11)10(8,2)3/h6-9H,4-5,11H2,1-3H3/t6-,7+,8-,9-/m1/s1

SMILES string

C[C@H]1[C@H](N)CC2CC1C2(C)C

InChI key

VPTSZLVPZCTAHZ-BZNPZCIMSA-N

assay

95%

form

liquid

optical activity

[α]21/D −42°, neat

refractive index

n20/D 1.48 (lit.)

bp

90 °C/18 mmHg (lit.)

density

0.909 g/mL at 25 °C (lit.)

Quality Level

100

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

161.6 °F - closed cup

flash_point_c

72 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBQ7835
SHBL3054
SHBF9684V
SHBD0088V
SHBB6337V

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

Wenhui Hu et al.
Journal of medicinal chemistry, 53(9), 3831-3834 (2010-04-17)
Although amantadine derivatives are the only M2 drugs for influenza virus A, their use is limited in the U.S. because of drug resistance. Here we report the identification of multiple M2 inhibitors that were rapidly generated through focused screening of

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