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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)-

9-Octadecen-1-ol, (9E)-

CCCCCCCC/C=C/CCCCCCCCO Request for Quotation
Chemical Name: 9-Octadecen-1-ol, (9E)-
CAS Number: 506-42-3
Product Number: AG003UYN(AGN-PC-0OBDJK)
Synonyms:
MDL No:
Molecular Formula: C18H36O
Molecular Weight: 268.47784

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
268.485g/mol
XLogP3:
7.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
15
Exact Mass:
268.277g/mol
Monoisotopic Mass:
268.277g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
175
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
1
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
Precautionary Statements:
P280
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

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Chemical Structure


Elaidyl Alcohol, also known as trans-9-Octadecen-1-ol, is a key ingredient utilized in chemical synthesis processes across various industries. This versatile compound is commonly employed as a precursor in the production of various organic compounds due to its unique chemical properties. In chemical synthesis, Elaidyl Alcohol serves as a valuable building block for creating a wide range of products, including pharmaceuticals, plastics, and flavors.One of the primary applications of Elaidyl Alcohol in chemical synthesis is its role as a starting material in the synthesis of fatty acids and their derivatives. By undergoing various chemical reactions such as oxidation, esterification, and hydrogenation, Elaidyl Alcohol can be transformed into important compounds like fatty aldehydes, esters, and acids. These derivatives find extensive use in the manufacturing of soaps, detergents, cosmetics, and food additives.Furthermore, Elaidyl Alcohol can be utilized in the production of surfactants and emulsifiers, which are essential components in various industrial processes. Its unique molecular structure enables it to participate in reactions that lead to the formation of surfactants with specific functionalities and properties, making them suitable for use in cleaning products, personal care items, and agricultural formulations.In addition to its applications in the production of fatty acids and surfactants, Elaidyl Alcohol can also be employed in the synthesis of specialty chemicals such as lubricants, plasticizers, and fragrances. Its ability to undergo diverse chemical transformations allows for the creation of tailored compounds that meet specific industry requirements, showcasing the significance of Elaidyl Alcohol in the realm of chemical synthesis.