1-Hexadecanol - CAS 36653-82-4
Catalog: |
BB023030 |
Product Name: |
1-Hexadecanol |
CAS: |
36653-82-4 |
Synonyms: |
hexadecan-1-ol |
Application: |
Hair care After Sun Products Body care Face care |
IUPAC Name: | hexadecan-1-ol |
Description: | Cetyl Alcohol is commonly used as an opacifier in shampoos, or as an emollient, emulsifier or thickening agent in the manufacture of skin creams and lotions. |
Molecular Weight: | 242.44 |
Molecular Formula: | C16H34O |
Canonical SMILES: | CCCCCCCCCCCCCCCCO |
InChI: | InChI=1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3 |
InChI Key: | BXWNKGSJHAJOGX-UHFFFAOYSA-N |
Boiling Point: | 344 °C |
Melting Point: | 49-54 °C |
Flash Point: | 275 °F |
Density: | 0.818 g/mL at 25 °C(lit.) |
Solubility: | Soluble in chloroform (slightly), methanol (slightly). |
Appearance: | White to off-white solid |
Storage: | Room Temperature |
Decomposition: | When heated to decomposition it emits acrid smoke and fumes |
MDL: | MFCD00004760 |
LogP: | 5.46000 |
Vapor Pressure: | <0.01 mm Hg ( 43 °C) |
GHS Hazard Statement: | H315 (33.71%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P391, P403+P233, P405, and P501 |
Signal Word: | Warning |
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PMID | Publication Date | Title | Journal |
30133268 | 20180919 | Sodorifen Biosynthesis in the Rhizobacterium Serratia plymuthica Involves Methylation and Cyclization of MEP-Derived Farnesyl Pyrophosphate by a SAM-Dependent C-Methyltransferase | Journal of the American Chemical Society |
22882126 | 20121201 | The effect of an amphiphilic self-assembled lipid lamellar phase on the relief of dry skin | International journal of cosmetic science |
22885112 | 20121115 | Diatomite-supported Pd-M (M=Cu, Co, Ni) bimetal nanocatalysts for selective hydrogenation of long-chain aliphatic esters | Journal of colloid and interface science |
22851616 | 20121101 | ATP serves as an endogenous inhibitor of UDP-glucuronosyltransferase (UGT): a new insight into the latency of UGT | Drug metabolism and disposition: the biological fate of chemicals |
22943173 | 20121001 | Biodegradable donepezil lipospheres for depot injection: optimization and in-vivo evaluation | The Journal of pharmacy and pharmacology |
Complexity: | 123 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 242.260965704 |
Formal Charge: | 0 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 242.260965704 |
Rotatable Bond Count: | 14 |
Topological Polar Surface Area: | 20.2 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 7.3 |
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