2-HYDROXYADAMANTANE

PRODUCT IDENTIFICATION

CAS NO. 700-57-2

2-HYDROXYADAMANTANE

EINECS NO. 211-846-7
FORMULA C10H15OH
MOL WT. 152.23

H.S. CODE

2906.19.5000

TOXICITY

 

SYNONYMS Tricyclo[3.3.1.13,7]decan-2-ol; 2-Adamantanol; Adamantan-2-ol;
2-Adamantanol;
SMILES C1C2CC3CC1CC(C3O)C2

CLASSIFICATION

 

EXTRA NOTES

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE white crystalline powder
MELTING POINT 258 -262 C
BOILING POINT

Decomposes

SPECIFIC GRAVITY  
SOLUBILITY IN WATER insoluble
pH  
VAPOR DENSITY

 

AUTOIGNITION

 

NFPA RATINGS

Health: 1; Flammability: 0; Reactivity: 0

REFRACTIVE INDEX

 
FLASH POINT

 

STABILITY

Stable under ordinary conditions

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking - Adamantane

Google Scholar Search

Drug Information Portal (U.S. National Library of Medicine) - 2-Hydroxyadamantane

PubChem Compound Summary - 2-Hydroxyadamantane

http://www.ebi.ac.uk/chebi/ - 2-Hydroxyadamantane

Local:
Adamantane consists of four cyclohexanes fused each other in chair conformations. It is the most stable isomer of formula, C10H16; one of  the highest melting point hydrocarbons (> 210 C); boiling point cannot be determined directly as it sublimes easily. Its stability is from strain free and highly symmetrical structure (all C-C bonds are set in and all Cs are tetrahedral). Its systematical name is tricyclo[3.3.1.1(3,7)]decane which means bicyclo[3.3.1]decane with an extra one-carbon bridge between C3 and C7. An alkyl substituent is axial in one ring and equatorial in another. Polymantanes have the same structure as the diamond lattice featuring highly symmetrical and strain free and are named as diamondoids . The general molecular formula of homologous diamondoid is C4n+6H4n+12. Diamondoids have one or more cages and are called diamantane, triamantane, and polymantanes. There are numerous structural isomers as well. Aadamantane itself is the simplest diamondoid. Some examples are; iceane (C12H18), diadamantane (C14H20), triadamantane (C18H24), isotetramantane (C22H28), cyclohexamantane (C26H30), superadamantane (C35H36). Natural diamondoids are extracted and purified from petroleum deposits. Diamondoids are being investigated in the new field of nanotechnoloy. Clinically, amantane and its derivatives are employed chiefly for the synthesis of antiviral drugs as well as neurological drugs such as rimantadine and Parkinson’s disease drugs. Their unique structures have the possibility to be applied to produce a broad range of biologically and pharmaceutically active drugs such as anticancer and anti-microbial agents. 1-Hydroxyadamantane is an intermediate for the synthesis of other adamantane derivatives and pharmaceuticals especially for Adapalene( used to treat acne) and Rimantadine (antiviral drug)

SALES SPECIFICATION

APPEARANCE

white crystalline powder

ASSAY (G.C)

99.0% min

MELTING POINT 258 -262 C
TRANSPORTATION
PACKING
 
HAZARD CLASS  
UN NO. Not regulated
SAFETY INFORMATION
EC DIRECTIVES

 

HAZARD CODES

 

RISK PHRASES

 

SAFETY PHRASES

22-24/25  

PRICE INFORMATION