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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)-

1,2,10-Decanetriol

OCCCCCCCCC(CO)O Request for Quotation
Chemical Name: 1,2,10-Decanetriol
CAS Number: 91717-85-0
Product Number: AG003D9G(AGN-PC-0570JF)
Synonyms:
MDL No:
Molecular Formula: C10H22O3
Molecular Weight: 190.27988

Identification/Properties

Properties
MP:
66℃
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
190.283g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
9
Exact Mass:
190.157g/mol
Monoisotopic Mass:
190.157g/mol
Topological Polar Surface Area:
60.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
96.2
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Decane-1,2,10-triol, also known as decanetriol, is a versatile compound that finds instrumental application in chemical synthesis. As a polyhydric alcohol containing three hydroxyl groups, decanetriol serves as a crucial building block for the production of various chemicals and materials. Its unique structure allows it to participate in a wide range of chemical reactions, leading to the synthesis of valuable products across different industries.In chemical synthesis, decanetriol plays a significant role as a multi-functional intermediate. Its hydroxyl groups can undergo reactions such as esterification, etherification, and oxidation, enabling the formation of complex organic compounds. Decanetriol's ability to form esters makes it particularly useful in the production of polymers, resins, and surfactants. Additionally, its presence in the synthesis of pharmaceuticals, flavors, and fragrances highlights its importance in the pharmaceutical and food industries.Moreover, decanetriol's aliphatic structure provides it with stability and compatibility in various formulations and processes. Its hydrophobic nature makes it a suitable additive in lubricants, plasticizers, and personal care products. The incorporation of decanetriol in these applications enhances their performance and properties, showcasing its versatility and utility in a wide array of chemical processes and industries.Overall, decane-1,2,10-triol's multifunctional properties make it a valuable compound in chemical synthesis, contributing to the creation of diverse products and materials that impact industries ranging from pharmaceuticals to cosmetics.