25276-70-4 Usage
Uses
Used in Chemical Synthesis:
N-Pentadecyl mercaptan is used as a chemical intermediate for the synthesis of various organic compounds, contributing to the production of a wide range of chemical products.
Used in Flavoring Agents:
In the food industry, N-Pentadecyl mercaptan is utilized as a flavoring agent, enhancing the taste and aroma of certain food products.
Used in Pharmaceutical Production:
N-Pentadecyl mercaptan serves as a raw material in the production of pharmaceuticals, playing a crucial role in the development of various medications.
Used in Agricultural Products:
N-PENTADECYL MERCAPTAN is also used as a raw material in the creation of agricultural products, supporting the growth and protection of crops.
Used in Rubber Chemicals:
N-Pentadecyl mercaptan is employed in the production of rubber chemicals, contributing to the manufacturing process of rubber goods.
Used in Natural Gas Odorization:
As an odorant in natural gas, N-Pentadecyl mercaptan provides a distinctive smell to facilitate the detection of gas leaks, ensuring safety in residential and industrial settings.
Used in Safety and Detection:
N-Pentadecyl mercaptan is used for safety and detection purposes, particularly in the identification of gas leaks, due to its strong and recognizable odor.
Check Digit Verification of cas no
The CAS Registry Mumber 25276-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,7 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25276-70:
(7*2)+(6*5)+(5*2)+(4*7)+(3*6)+(2*7)+(1*0)=114
114 % 10 = 4
So 25276-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H32S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16/h16H,2-15H2,1H3
25276-70-4Relevant academic research and scientific papers
Intrinsic and Extrinsic Control of the p Ka of Thiol Guests inside Yoctoliter Containers
Cai, Xiaoyang,Kataria, Rhea,Gibb, Bruce C.
supporting information, p. 8291 - 8298 (2020/05/28)
Despite decades of research, there are still many open questions surrounding the mechanisms by which enzymes catalyze reactions. Understanding all the noncovalent forces involved has the potential to allow de novo catalysis design, and as a step toward this, understanding how to control the charge state of ionizable groups represents a powerful yet straightforward approach to probing complex systems. Here we utilize supramolecular capsules assembled via the hydrophobic effect to encapsulate guests and control their acidity. We find that the greatest influence on the acidity of bound guests is the location of the acidic group within the yoctoliter space. However, the nature of the electrostatic field generated by the (remote) charged solubilizing groups also plays a significant role in acidity, as does counterion complexation to the outer surfaces of the capsules. Taken together, these results suggest new ways by which to affect reactions in confined spaces.
