62732-71-2 Usage
Molecular weight
300.54 g/mol The molecular weight of 1-Heptadecanol, methanesulfonate is 300.54 grams per mole, which indicates the mass of one mole of the compound.
Surfactant and wetting agent
Industrial applications 1-Heptadecanol, methanesulfonate is commonly used as a surfactant and wetting agent in various industrial processes, such as the production of plastics, coatings, and adhesives.
Long-chain alcohol
Classification 1-Heptadecanol, methanesulfonate is classified as a long-chain alcohol due to its 17 carbon atoms in the alcohol chain.
Methanesulfonate form
High solubility The methanesulfonate form of 1-Heptadecanol is often preferred in industrial processes because of its high solubility in both polar and non-polar solvents.
Biodegradability
Environmentally friendly 1-Heptadecanol, methanesulfonate has good biodegradability, which means it can be broken down by microorganisms in the environment, making it more environmentally friendly.
Low toxicity
Safe for use The compound has low toxicity, making it safe for use in various manufacturing processes without posing significant health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 62732-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62732-71:
(7*6)+(6*2)+(5*7)+(4*3)+(3*2)+(2*7)+(1*1)=122
122 % 10 = 2
So 62732-71-2 is a valid CAS Registry Number.
62732-71-2Relevant academic research and scientific papers
Synthesis of alkyl [(alkyl 6-deoxy-alpha-D-gluco-heptopyranosyl- uronate) 6-deoxy-alpha-D-gluco-heptopyranosid]uronates, a novel type of mirror pseudo cord factor.
Baer,Breton
, p. 181 - 189 (2007/10/02)
The 1-octyl, 1-pentadecyl, 1-hexadecyl, 1-heptadecyl, and 1-octadecyl diesters of (6-deoxy-alpha-D-gluco-heptopyranosyluronic acid) 6-deoxy-alpha-D-gluco-heptopyranosiduronic acid, a new homolog of trehalosuronic acid, were prepared by two procedures. One procedure involved conversion of the peracetylated acid into its dichloride, reaction of the latter with the alkanols, and acid-catalyzed deacetylation of the products, whereas the other consisted of reaction of alkyl mesylates with the potassium salt of the unprotected acid.
