Skip to Content
Merck
CN

523690

3-Amino-1-adamantanol

96%

Synonym(s):

(3-Hydroxyadamantan-1-yl)amine, 1-Amino-3-adamantanol, 1-Amino-3-hydroxyadamantane, 3-Amino-1-hydroxyadamantane, 3-Aminotricyclo[3.3.1.13,7]decan-1-ol

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C10H17NO
CAS Number:
Molecular Weight:
167.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
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

3-Amino-1-adamantanol, 96%

InChI

1S/C10H17NO/c11-9-2-7-1-8(3-9)5-10(12,4-7)6-9/h7-8,12H,1-6,11H2/t7-,8+,9+,10-

SMILES string

N[C@]12C[C@@H]3C[C@H](C1)C[C@@](O)(C3)C2

InChI key

DWPIPTNBOVJYAD-FIRGSJFUSA-N

assay

96%

form

solid

mp

265 °C (dec.) (lit.)

functional group

hydroxyl

Quality Level

Related Categories

Application

Employed in the synthesis of inhibitors with antihyperglycemic properties.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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

Ramzia I El-Bagary et al.
International journal of biomedical science : IJBS, 7(3), 201-208 (2011-09-01)
Two reversed-phase liquid chromatographic (RP-LC) methods are described for the determination of two binary mixtures of hypoglycemic agents. In the first method, vildagliptin (VDG) was determined in the presence of 3-amino-1-adamantanol (AAD), a synthetic intermediate and impurity of VDG. In
A Facile and Economical Method to Synthesize Vildagliptin.
Deng Y, et al.
Letters in Organic Chemistry, 11(10), 780-784 (2014)
Nieves Fresno et al.
PloS one, 9(12), e113841-e113841 (2014-12-02)
Paracetamol also known as acetaminophen, is a widely used analgesic and antipyretic agent. We report the synthesis and biological evaluation of adamantyl analogues of paracetamol with important analgesic properties. The mechanism of nociception of compound 6a/b, an analog of paracetamol
NOVEL TRICYCLIC CYANOPYRROLIDINE DERIVATIVES AS DPP4 INHIBITORS: AN IMPROVED SYNTHESIS OF TRICYCLIC a-CYCNOPYRROLIDINE FROM CAMPHOR.
Arumugam K and Anitha M.
Rasayan Journal of Chemistry, 6(3), 230-237 (2013)
Edwin B Villhauer et al.
Journal of medicinal chemistry, 46(13), 2774-2789 (2003-06-13)
Dipeptidyl peptidase IV (DPP-IV) inhibition has the potential to become a valuable therapy for type 2 diabetes. The synthesis and structure-activity relationship of a new DPP-IV inhibitor class, N-substituted-glycyl-2-cyanopyrrolidines, are described as well as the path that led from clinical

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