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  • 12441-09-7, 1,4 -去水山梨醇, 国产现货高纯1,4-Sorbitan, CAS:12441-09-7
12441-09-7, 1,4 -去水山梨醇, 国产现货高纯1,4-Sorbitan, CAS:12441-09-7

12441-09-7, 1,4 -去水山梨醇, 国产现货高纯1,4-Sorbitan, CAS:12441-09-7

12441-09-7 ,1,4 -去水山梨醇, 异山梨醇杂质8
1,4-Sorbitan,
CAS:12441-09-7
C6H12O5 / 164.16
MFCD00272634
In stock.国产现货高纯,白色结晶粉末。
吐温,司盘起始原料。

1,4 -去水山梨醇,   1,4-Anhydro-D-glucitol

国产现货高纯,白色结晶粉末。吐温,司盘起始原料。

Intermediate in the synthesis of prostaglandins.

Sorbitan is a versatile chemical compound used in various fields of research and industry due to its unique physical and chemical properties. It is a natural polyol ester derived from sorbitol and fatty acids, and it has been used as an emulsifier, surfactant, plasticizer, and lubricant. Sorbitan is widely utilized in the pharmaceutical, food, cosmetics, and textile industries. This paper aims to provide an overview of sorbitan, its physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions.

Definition and Background

Sorbitan is a naturally occurring polyol ester and is commonly used as a surfactant, emulsifying agent, and plasticizer. It is obtained by esterification of sorbitol with various fatty acids derived from vegetable oils. The most common fatty acids used in the synthesis of sorbitan esters are lauric, stearic, oleic, and palmitic acids. Sorbitan esters are widely used in the food, cosmetic, and pharmaceutical industries due to their biodegradability, low toxicity, and excellent emulsifying properties.

Physical and Chemical Properties

Sorbitan esters are usually white to yellowish waxy solids with a low melting point. They are soluble in water, ethanol, and ether, and insoluble in hydrocarbons. The polarity of sorbitan esters depends on the fatty acid used in their synthesis. Sorbitan esters with shorter chain fatty acids are more polar than those with longer chain fatty acids. This polarity affects the surface activity and emulsifying properties of sorbitan esters. Sorbitan esters are stable under normal storage conditions and exhibit good oxidative stability.

Synthesis and Characterization

Sorbitan esters are synthesized by esterification of sorbitol with various fatty acids derived from vegetable oils. The esterification is usually catalyzed by acid catalysts such as sulfuric acid or p-toluenesulfonic acid. The synthesized sorbitan esters are purified by washing with water and recrystallization from ethanol.

The characterization of sorbitan esters is usually done by various analytical techniques such as infrared (IR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, gas chromatography (GC), high-performance liquid chromatography (HPLC), and mass spectrometry (MS). These techniques are used to determine the identity, purity, and quantity of sorbitan esters.

Analytical Methods

Analytical methods are used to determine the purity and quality of sorbitan esters. The most commonly used analytical techniques are HPLC and GC. These methods are used to determine the identity, purity, and quantity of sorbitan esters. Other techniques such as IR, NMR, and MS are also used for the characterization of sorbitan esters.

Biological Properties

Sorbitan esters have been used as food additives, cosmetics, and pharmaceuticals for many years. Sorbitan esters are generally considered safe and have low toxicity. However, some studies have shown that some sorbitan esters can cause skin irritation and allergic reactions in certain individuals. Sorbitan esters are also known to be biodegradable and have low environmental impact.

Toxicity and Safety in Scientific Experiments

Sorbitan esters have been widely used in scientific experiments and are generally considered safe and have low toxicity. In most cases, sorbitan esters are used at low concentrations. However, some studies have shown that some sorbitan esters can cause skin irritation and allergic reactions in certain individuals. It is important to follow the safety guidelines and use appropriate protective equipment when working with sorbitan esters.

Applications in Scientific Experiments

Sorbitan esters are widely used in scientific experiments due to their unique physical and chemical properties. Sorbitan esters are used as emulsifiers, surfactants, and lubricants in various fields of research. They are used in the cosmetics industry as emulsifiers and stabilizers for creams and lotions. In the pharmaceutical industry, sorbitan esters are used as solubilizers for poorly soluble drugs. In the textile industry, sorbitan esters are used as emulsifiers and lubricants for the manufacturing of synthetic fibers.

Current State of Research

Research on sorbitan esters has been ongoing for many years, and new applications and uses are constantly being discovered. Recent research has focused on the synthesis of new sorbitan esters with enhanced properties, such as improved emulsifying properties, increased stability, and reduced toxicity. Research has also focused on the application of sorbitan esters in the development of novel drug delivery systems and in the formulation of stable and effective cosmetic products.

Potential Implications in Various Fields of Research and Industry

Sorbitan esters have potential implications in various fields of research and industry. In the food industry, sorbitan esters are used as emulsifiers and stabilizers for various food products. In the pharmaceutical industry, sorbitan esters are used as solubilizers for poorly soluble drugs and in the development of novel drug delivery systems. In the cosmetics industry, sorbitan esters are used as emulsifiers, stabilizers, and solubilizers. In the textile industry, sorbitan esters are used as lubricants and emulsifiers.

Limitations and Future Directions

One of the limitations of sorbitan esters is their limited solubility in hydrocarbons. Future research could focus on the development of new sorbitan esters with increased solubility in hydrocarbons. Another area of future research could be the development of sorbitan esters with enhanced emulsifying properties and stability. In addition, research could focus on the development of new applications for sorbitan esters in various fields of research and industry such as nanotechnology and biotechnology.

CAS Number12441-09-7
Product NameSorbitan
IUPAC Name(2R,3R,4S)-2-[(1R)-1,2-dihydroxyethyl]oxolane-3,4-diol
Molecular FormulaC6H12O5
Molecular Weight164.16 g/mol
InChIInChI=1S/C6H12O5/c7-1-3(8)6-5(10)4(9)2-11-6/h3-10H,1-2H2/t3-,4+,5-,6-/m1/s1
InChI KeyJNYAEWCLZODPBN-JGWLITMVSA-N
SMILESC1C(C(C(O1)C(CO)O)O)O
Synonyms1,4-Anhydro-D-glucitol; 1,4-Anhydroglucitol; 1,4-Sorbitan;
Canonical SMILESC1C(C(C(O1)C(CO)O)O)O
Isomeric SMILESC1[C@@H]([C@H]([C@H](O1)[C@@H](CO)O)O)O


CAS No: 12441-09-7 Synonyms: 1,4-Anhydro-D-sorbitol1,4-Sorbitan MDL No: MFCD00272634 Chemical Formula: C6H12O5 Molecular Weight: 164.16

In stock.

国产现货高纯,白色结晶粉末。

References: 1. Bashford VG, Wiggins LF, J. Chem. Soc. 1948, p299


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