27991-81-7 Usage
General Description
8-Aminooctanoic acid HCl, also known as caprylic acid, is a chemical compound commonly used in the production of pharmaceuticals and personal care products. It is a derivative of the naturally occurring fatty acid, caprylic acid, and is typically used as a precursor in the synthesis of various bioactive compounds. This chemical is known for its antibacterial and antifungal properties, making it a valuable ingredient in the formulation of topical medications and antiseptic solutions. Additionally, 8-Aminooctanoic acid HCl has been found to have potential applications in the treatment of neurodegenerative diseases due to its ability to modulate the activity of certain neurotransmitters. Overall, this compound has a wide range of applications in the pharmaceutical and personal care industries, making it a valuable chemical in various product formulations.
Check Digit Verification of cas no
The CAS Registry Mumber 27991-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,9 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 27991-81:
(7*2)+(6*7)+(5*9)+(4*9)+(3*1)+(2*8)+(1*1)=157
157 % 10 = 7
So 27991-81-7 is a valid CAS Registry Number.
27991-81-7Relevant articles and documents
Transkarbams as transdermal permeation enhancers: Effects of ester position and ammonium carbamate formation
Novotny, Michal,Hrabálek, Alexandr,Jan??ová, Barbora,Novotny, Jakub,Vávrová, Kate?ina
scheme or table, p. 2726 - 2728 (2010/08/04)
Transkarbam 12, an ammonium carbamate formed by the reaction of dodecyl 6-aminohexanoate with carbon dioxide, is a highly active, broad-spectrum, nontoxic, and nonirritant transdermal permeation enhancer. It probably acts by a dual mechanism: a part of its activity is associated with the carbamic acid salt and/or its decomposition in the acidic stratum corneum. The ammonium ester thereby released is an active enhancer species as well, and its activity highly depends on the position of the ester group.
