CAS 927-45-7

7-Tridecanol

Description:

7-Tridecanol, with the CAS number 927-45-7, is a long-chain fatty alcohol characterized by its linear structure consisting of a 13-carbon chain with a hydroxyl (-OH) group located at the seventh carbon. This compound is a colorless, viscous liquid at room temperature and is known for its hydrophobic properties, making it insoluble in water but soluble in organic solvents. It has a relatively high boiling point and low volatility, typical of long-chain alcohols. 7-Tridecanol is primarily used in the production of surfactants, emulsifiers, and lubricants, as well as in the formulation of personal care products due to its moisturizing properties. Additionally, it can serve as a precursor in the synthesis of various chemical compounds. Its fatty alcohol nature contributes to its mildness and compatibility with skin, making it a valuable ingredient in cosmetic formulations. Safety data indicates that, while it may cause mild irritation upon contact, it is generally considered safe for use in regulated applications.

Formula: C₁₃H₂₈O

InChI: InChI=1S/C13H28O/c1-3-5-7-9-11-13(14)12-10-8-6-4-2/h13-14H,3-12H2,1-2H3

InChI key: InChIKey=KWUWHKRBPALTGJ-UHFFFAOYSA-N

SMILES: C(C(CCCCCC)O)CCCCC

Synonyms:

• 7-Tridecanol
• 7-tridecanol
• Tridecan-7-ol
• NSC 158536
• 1-Hexyl-1-heptanol

7-​Tridecanol

CAS: 927-45-7

Formula: C₁₃H₂₈O

Purity: 98%

Color and Shape: Solid

Molecular weight: 200.3608

Ref: IN-DA006EIY

7-​Tridecanol

CAS: 927-45-7

7-​Tridecanol

Purity: 98%

Molecular weight: 200.36g/mol

Ref: 54-OR1042879

7-TRIDECANOL

CAS: 927-45-7

Purity: 98%

Molecular weight: 200.3659973

Ref: 10-F844022

7-Tridecanol

CAS: 927-45-7

7-Tridecanol is a homologous fatty acid, which is a type of lipid that consists of three long chain hydrocarbons. It is biodegradable and has been shown to have structural isomers. 7-Tridecanol has been shown to be an effective anti-cancer agent in vivo, particularly against mouse melanoma. The mechanism of action of 7-tridecanol is not known, but it may inhibit carboxylate groups or reversibly form acetyl derivatives with the cell membrane. This compound also inhibits the activity of primers by competitively binding to DNA at the 3' position during the polymerase chain reaction (PCR) process.

Formula: C₁₃H₂₈O

Purity: Min. 95%

Molecular weight: 200.36 g/mol

Ref: 3D-AAA92745