Skip to Content
Merck
All Photos(1)

Documents

130346

Sigma-Aldrich

1-Adamantanol

ReagentPlus®, 99%

Synonym(s):

1-Hydroxyadamantane

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

About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
768-95-6
Molecular Weight:
152.23
Beilstein:
1903952
EC Number:
212-202-8
MDL number:
MFCD00074729
UNSPSC Code:
12352100
PubChem Substance ID:
24847960
NACRES:
NA.22

product line

ReagentPlus®

Assay

99%

form

powder

mp

247 °C (subl.) (lit.)

SMILES string

OC12C[C@H]3C[C@H](C[C@H](C3)C1)C2

InChI

1S/C10H16O/c11-10-4-7-1-8(5-10)3-9(2-7)6-10/h7-9,11H,1-6H2/t7-,8+,9-,10-

InChI key

VLLNJDMHDJRNFK-CHIWXEEVSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

1-Adamantanol was used in the preparation of 1,3-adamantanediol.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Motowo Yamaguchi et al.
Inorganic chemistry, 45(20), 8342-8354 (2006-09-27)
New ruthenium(II) complexes having a tetradentate ligand such as tris(2-pyridylmethyl)amine (TPA), tris[2-(5-methoxycarbonyl)pyridylmethyl]amine [5-(MeOCO)3-TPA], tris(2-quinolylmethyl)amine (TQA), or bis(2-pyridylmethyl)glycinate (BPG) have been prepared. The reaction of the ligand with [RuCl2(Me2SO)4] resulted in a mixture of trans and cis isomers of the chloro(dimethyl
Koichi Mitsukura et al.
Journal of bioscience and bioengineering, 109(6), 550-553 (2010-05-18)
To efficiently produce 1,3-adamantanediol (1,3-ad(OH)(2)) from 1-adamantanol (1-adOH), our stocks of culture strains and soil microorganisms were surveyed for hydroxylation activity towards 1-adOH. Among them, the soil actinomycete SA8 showing the highest hydroxylation activity was identified as Streptomyces sp. based

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