1005-68-1 Usage
Description
Isopentylcyclopentane, with the molecular formula C11H20, is a cycloalkane compound characterized by a five-membered cyclopentane ring to which an isopentyl group—a branched chain of five carbon atoms—is attached. This colorless liquid at room temperature is recognized for its utility in various industrial applications, particularly as a solvent, and is also valued in the production of perfumes and as a fragrance ingredient in cosmetic products. Notably, Isopentylcyclopentane is not known to pose significant toxic effects on humans or the environment.
Uses
Used in Industrial Processes:
Isopentylcyclopentane is used as a solvent for its ability to dissolve a wide range of substances, facilitating various chemical reactions and processes in the industry.
Used in Perfumery:
Isopentylcyclopentane is used as a fragrance ingredient in perfumes, leveraging its aromatic properties to contribute to the scent profiles of different perfumed products.
Used in Cosmetic Products:
Isopentylcyclopentane is utilized in the formulation of cosmetic products, where it serves as a fragrance component, enhancing the sensory experience of the products while maintaining safety and minimal environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 1005-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1005-68:
(6*1)+(5*0)+(4*0)+(3*5)+(2*6)+(1*8)=41
41 % 10 = 1
So 1005-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H20/c1-9(2)7-8-10-5-3-4-6-10/h9-10H,3-8H2,1-2H3
1005-68-1Relevant articles and documents
Thiotolerant Ir/SiO2-Al2O3 bifunctional catalysts: Effect of metal-acid site balance on tetralin hydroconversion
Nassreddine, Salim,Massin, Laurence,Aouine, Mimoun,Geantet, Christophe,Piccolo, Laurent
, p. 253 - 265 (2011)
The hydroconversion of tetralin over iridium nanoparticles supported on amorphous silica-alumina (ASA) has been investigated in a continuous high-pressure gas-phase micro-reactor in the presence of H2S. In order to tune the Ir particle size, the bifunctional Ir/ASA catalysts have been submitted to sintering treatments. The samples have been characterized by HRTEM and XPS. From careful analysis of tetralin conversion products by comprehensive two-dimensional gas chromatography (GC×GC-MS) and NMR, compound families have been unambiguously distinguished. Hydrogenation, dehydrogenation, (saturated and aromatic) ring-contraction products, and (saturated and aromatic) one-ring-opening products are formed, without significant cracking. The catalysts exhibit stable activity in the presence of sulfur. As the mean particle size increases from 1.5 to 8 nm, the ring-opening/contraction selectivity increases dramatically. This effect is related to an increase of the acid/metal site ratio.