1,9-Nonanediol
[CAS# 3937-56-2]

Identification

• Classification: Chemical reagent >> Organic reagent >> Fatty alcohol
• Name: 1,9-Nonanediol
• Synonyms: Nonamethylene glycol
• Molecular Formula: C₉H₂₀O₂
• Molecular Weight: 160.25
• CAS Registry Number: 3937-56-2
• EC Number: 223-517-5
• SMILES: C(CCCCO)CCCCO

Properties

• Density: 0.9±0.1 g/cm³ Calc.^*, 0.95 g/mL (Expl.)
• Melting point: 45 - 47 ºC (Expl.)
• Boiling point: 292.4±8.0 ºC 760 mmHg (Calc.)^*, 340.3 ºC (Expl.)
• Flash point: 137.0±13.0 ºC (Calc.)^*, 113 ºC (Expl.)
• Index of refraction: 1.456 (Calc.)^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS07 Warning
• Hazard Statements: H315-H319-H335-H412
• Precautionary Statements: P261-P264-P264+P265-P271-P273-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Chronic hazardous to the aquatic environment	Aquatic Chronic	3	H412
Skin irritation	Skin Irrit.	2	H315
Eye irritation	Eye Irrit.	2	H319
Specific target organ toxicity - single exposure	STOT SE	3	H335

Discovory and Applicatios

1,9-Nonanediol is an aliphatic diol consisting of a nine-carbon linear hydrocarbon chain with hydroxyl groups attached to both terminal carbons. Its molecular formula is C₉H₂₀O₂. As an α,ω-diol, it features two primary alcohol functional groups separated by a seven-carbon methylene chain, placing it within the class of linear long-chain diols commonly used as intermediates in polymer synthesis and specialty chemical manufacturing.

The synthesis of 1,9-nonanediol is often achieved by catalytic hydrogenation of the corresponding dicarboxylic acid, nonanedioic acid (azelaic acid), or its derivatives such as esters or acid chlorides. Catalysts such as Raney nickel or copper chromite under elevated temperatures and pressures facilitate the reduction of the carboxyl groups to primary alcohols. Alternative routes may involve multi-step synthetic sequences starting from shorter-chain precursors with subsequent carbon chain extension.

1,9-Nonanediol’s bifunctional alcohol groups enable it to serve as a key monomer or intermediate in the preparation of polyesters, polyurethanes, and other polymers. Its flexible nine-carbon alkyl backbone contributes to polymer chain flexibility, hydrophobicity, and thermal stability. When used in polyester synthesis, 1,9-nonanediol reacts with dicarboxylic acids to form polymers with desirable mechanical properties and moderate crystallinity, applicable in fibers, coatings, adhesives, and biodegradable materials.

The diol is also utilized in the synthesis of surfactants, plasticizers, and lubricant additives. Chemical modifications such as esterification or etherification of the hydroxyl groups generate amphiphilic molecules useful in detergents, emulsifiers, and personal care formulations. The balance of hydrophilic alcohol termini and hydrophobic alkyl chain facilitates interactions with both polar and nonpolar phases.

Physically, 1,9-nonanediol is typically a colorless to pale yellow solid with a melting point reflective of its chain length and purity. It is sparingly soluble in water but dissolves well in organic solvents including alcohols, ethers, and hydrocarbons. The compound is chemically stable under ambient conditions but can be sensitive to strong oxidizing agents or acidic/basic hydrolysis.

Toxicological assessments indicate low acute toxicity and good biodegradability, supporting its use in environmentally compatible chemical manufacturing. It can be derived from renewable feedstocks, such as bio-based dicarboxylic acids, aligning with sustainable and green chemistry principles.

In summary, 1,9-nonanediol is a versatile bifunctional alcohol widely used in polymer chemistry, specialty chemical synthesis, and materials science. Its chemical reactivity, physical properties, and potential bio-based origins make it a valuable intermediate in diverse industrial and research applications.

References

2023. Synthesis and Characterization of Novel Hydrolytically Degradable Polyesters. Journal of Wuhan University of Technology-Mater. Sci. Ed., 38(4).
DOI: 10.1007/s11595-023-2720-6

2022. Degradable Polyesters based on Oxygenated Fatty Acid Monomer. Journal of Wuhan University of Technology-Mater. Sci. Ed., 37(5).
DOI: 10.1007/s11595-022-2592-1

2013. Synthesis and Characterization of Novel Diol, Diacid and Di-isocyanate from Oleic Acid. Journal of the American Oil Chemists' Society, 90(12).
DOI: 10.1007/s11746-013-2376-z