2-METHYL-2-ADAMANTANOL

PRODUCT IDENTIFICATION

CAS NO. 702-98-7

2-METHYL-2-ADAMANTANOL

EINECS NO.  
FORMULA C11H18O
MOL WT. 166.26

H.S. CODE

2906.19.5000

TOXICITY

 
SYNONYMS 2-Methyl Tricyclo(3.3.1.1(3,7))decan-2-ol; 2-Methyl-2-adamantanol;
2-Methyl-2-hydroxytricyclo[3.3.1.1(3,7)] decane;
SMILES C1(C2CC3CC1CC(C2)C3)(O)C

CLASSIFICATION

 

EXTRA NOTES

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE white crystalline powder
MELTING POINT 214 - 218 C
BOILING POINT

 

SPECIFIC GRAVITY > 1.0
SOLUBILITY IN WATER Insoluble
pH  
VAPOR DENSITY

 

AUTOIGNITION

 

NFPA RATINGS

Health: 2; Flammability: 0; Reactivity: 0

REFRACTIVE INDEX

 
FLASH POINT

 

STABILITY

Stable under ordinary conditions.

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking - Adamantane

Google Scholar Search

PubChem Compound Summary - 2-Methyl-2-adamantanol

KEGG (Kyoto Encyclopedia of Genes and Genomes) -  2-Methyl-2-adamantanol

http://www.ebi.ac.uk/chebi/ - 2-Methyl-2-adamantanol

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.

SALES SPECIFICATION

APPEARANCE

white to off-white powder

ASSAY

98.0% min

MELTING POINT

214 - 218 C

WATER

0.05% max

TRANSPORTATION
PACKING
 
HAZARD CLASS  
UN NO.  
OTHER INFORMATION
Hazard Symbols: XN, Risk Phrases: 20/21/22, Safety Phrases: 36
PRICE INFORMATION