1. Home
  2. Tetradecanoic acid, 14-hydroxy-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Tetradecanoic acid, 14-hydroxy-

OCCCCCCCCCCCCCC(=O)O Request for Quotation
Chemical Name: Tetradecanoic acid, 14-hydroxy-
CAS Number: 17278-74-9
Product Number: AG003ACU(AGN-PC-0KP0F8)
Synonyms:
MDL No:
Molecular Formula: C14H28O3
Molecular Weight: 244.3703

Identification/Properties

Computed Properties
Molecular Weight:
244.375g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
13
Exact Mass:
244.204g/mol
Monoisotopic Mass:
244.204g/mol
Topological Polar Surface Area:
57.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
169
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


14-Hydroxytetradecanoic acid is a crucial compound in chemical synthesis, particularly in the field of organic chemistry. It serves as a versatile building block for the creation of various derivatives and specialized compounds due to its unique structural properties.In chemical synthesis, 14-Hydroxytetradecanoic acid is utilized as a key precursor in the production of biologically active molecules, pharmaceuticals, and fine chemicals. Its hydroxyl group (-OH) and long hydrocarbon chain make it an ideal starting material for the creation of esters, ethers, and amides through various chemical reactions.One of the prominent applications of 14-Hydroxytetradecanoic acid is in the synthesis of surfactants and emulsifiers. By modifying the hydroxyl group or the hydrocarbon chain, chemists can tailor the properties of the resulting compounds for use in cosmetics, personal care products, and industrial applications. Additionally, 14-Hydroxytetradecanoic acid derivatives can be incorporated into lubricants, coatings, and polymers to enhance their performance characteristics.Furthermore, this compound plays a significant role in the development of novel materials such as bio-based polymers and biodegradable surfactants, contributing to the advancement of sustainable chemistry practices. Its structural versatility and reactivity make it a valuable asset in the realm of chemical synthesis, enabling the creation of diverse and functional chemical compounds with a wide range of applications.