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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Heptadecanol

CCCCCCCCCCCCCCCCCO Request for Quotation
Chemical Name: Heptadecanol
CAS Number: 1454-85-9
Product Number: AG001KVB(AGN-PC-0JKC2V)
Synonyms:
MDL No:
Molecular Formula: C17H36O
Molecular Weight: 256.4671

Identification/Properties

Properties
MP:
51-55 °C(lit.)
BP:
308.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.4324 (estimate)
Solubility:
chloroform: soluble50mg/mL, clear, colorless
Computed Properties
Molecular Weight:
256.474g/mol
XLogP3:
7.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
15
Exact Mass:
256.277g/mol
Monoisotopic Mass:
256.277g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
134
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Heptadecan-1-ol, also known as heptadecanol, is a long-chain primary alcohol with the chemical formula C17H36O. This compound plays a significant role in chemical synthesis, particularly in organic chemistry and material science.In chemical synthesis, heptadecan-1-ol can serve as a precursor for the synthesis of various esters, ethers, and other organic compounds. Its primary hydroxyl group can undergo reactions such as esterification and etherification to form derivatives with different functional groups. These derivatives can be further utilized in the production of fragrances, flavors, surfactants, lubricants, and pharmaceutical compounds.Heptadecan-1-ol can also be used as a building block in the synthesis of polymers and dendrimers. Its long hydrocarbon chain provides opportunities for creating functionalized molecules with specific properties. By incorporating heptadecan-1-ol into polymer structures, researchers can tailor the physical and chemical characteristics of the resulting materials for various applications in coatings, adhesives, and other industrial products.Additionally, heptadecan-1-ol is employed in the design and fabrication of self-assembled monolayers (SAMs) on solid surfaces. SAMs play a crucial role in nanotechnology and surface chemistry by providing well-ordered organic interfaces with controlled properties. By utilizing heptadecan-1-ol as a building block for SAMs, researchers can engineer surfaces with desired functionalities such as hydrophobicity, biocompatibility, and molecular recognition.Overall, heptadecan-1-ol's versatility in chemical synthesis makes it a valuable compound for creating a wide range of organic molecules, materials, and surface coatings with tailored properties for diverse applications in industry and research.