19780-33-7 Usage
General Description
2-Ethyl-1-dodecanol, also known as 2-ethylhexyl laurate, is a fatty alcohol that belongs to the chemical class of alcohols. It is a colorless liquid with a faint odor, and is insoluble in water but soluble in most organic solvents. This chemical is widely used as an intermediate in the production of various chemical compounds, such as detergents, lubricants, and fragrances. It is also utilized as a surfactant in the formulation of personal care products, cosmetics, and pharmaceuticals. Additionally, 2-ethyl-1-dodecanol has properties that make it suitable for use as a plasticizer in the manufacturing of PVC and other polymers, as well as a lubricant additive in metalworking fluids and industrial oils.
Check Digit Verification of cas no
The CAS Registry Mumber 19780-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,8 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19780-33:
(7*1)+(6*9)+(5*7)+(4*8)+(3*0)+(2*3)+(1*3)=137
137 % 10 = 7
So 19780-33-7 is a valid CAS Registry Number.
19780-33-7Relevant articles and documents
Ethyl-branched aldehydes, ketones, and diketones from caimans (Caiman and Paleosuchus; Crocodylia, Reptilia)
Krueckert, Karsten,Flachsbarth, Birte,Schulz, Stefan,Hentschel, Ute,Weldon, Paul J.
, p. 863 - 870 (2008/09/20)
Secretions from the paracloacal glands of alligators (Alligator spp.) and caimans (Caiman spp., Melanosuchus niger, and Paleosuchus spp.) were examined by GC-MS. The secretions of the common caiman (C. crocodilus), the broad-snouted caiman (C. latirostris), the yacare caiman (C. yacare), the dwarf caiman (P. palpebrosus), and the smooth-fronted caiman (P. trigonatus) yielded a new family of 43 aliphatic carbonyl compounds that includes aldehydes, ketones, and β-diketones with an ethyl branch adjacent to the carbonyl group. The identification of these glandular components and the syntheses and stereochemical investigations of selected compounds are described.
