Dodecanoic acid (Lauric acid)

Dodecanoic acid structural formula

CAS Number143-07-7
Molecular FormulaC12H24O2
Molecular Weight200.323
InChI KeyPOULHZVOKOAJMA-UHFFFAOYSA-N
LogP4.60
Synonyms
  • Dodecanoic acid
  • 143-07-7
  • Lauric acid
  • 1-Undecanecarboxylic acid
  • 4-02-00-01082
  • Acide laurique
  • acido laurico, puro
  • Aliphat No. 4
  • Dedaconoic acid
  • Dodecoic acid
  • Dodecylic acid
  • Edenor C 1298-100
  • Hystrene 9512
  • Kortacid 1299
  • Laurinsaure
  • Laurostearic acid
  • n-Dodecanoic acid
  • Neo-Fat 12-43
  • Nissan NAA 122
  • NSC 5026
  • Philacid 1200
  • Prifac 2920
  • Prifac 2922
  • Univol U 314
  • Vulvic acid
  • BRN 1099477
  • EINECS 205-582-1
  • FEMA No. 2614
  • Hydrofol acid 1255
  • Hydrofol acid 1295
  • Ninol AA62 Extra
  • NSC-5026
  • Univol U-314
  • Wecoline 1295
  • UNII-1160N9NU9U
  • 1-Undecanecarboxylate
  • ABL
  • C12 fatty acid
  • C12:0
  • CH3-[CH2]10-COOH
  • Coconut oil fatty acids
  • DAO
  • Dodecylate
  • Dodecylcarboxylate
  • Duodecyclic acid
  • Duodecylic acid
  • Emery 651
  • Laurate
  • Laurinsaeure
  • Laurostearate
  • Lunac L 70
  • Lunac L 98
  • N-Dodecanoate
  • Neo-Fat 12
  • Undecane-1-carboxylic acid
  • Vulvate
  • 203714-07-2
  • 7632-48-6
  • 8000-62-2
  • 8045-27-0

Applications:

HPLC Method for Analysis of Lauric acid on Newcrom BH Column

July 10, 2023

HPLC Method for Analysis of Dodecanoic acid (Lauric acid) on Newcrom BH by SIELC Technologies

Separation type: Liquid Chromatography Mixed-mode

HPLC Method for Analysis of Lauric acid on Newcrom BH Column by SIELC Technologies
HPLC Method for Separation of Dodecanoic acid (Lauric acid)

Lauric acid, also known as dodecanoic acid, is a saturated fatty acid. Its chemical formula is CH₃(CH₂)₁₀COOH. It is white in color, and it is a solid at room temperature with a melting point of around 44 degrees Celsius (111 degrees Fahrenheit). It is relatively inexpensive and has a long shelf life, which makes it an attractive ingredient in various commercial products.

Lauric acid is found naturally in various plant and animal fats and oils, but the largest amounts of lauric acid are found in coconut oil and palm kernel oil. In these oils, lauric acid can make up to 50% of the total fat content.

Lauric acid is commonly used in the manufacturing of soaps and cosmetics due to its ability to form a lather when mixed with water. It is also used in food for its role in digestion and metabolic processes. It’s a medium-chain fatty acid, which means it is more easily absorbed and utilized by the body compared to long-chain fatty acids.

Research suggests that lauric acid may have several health benefits. For instance, it is believed to have antimicrobial properties, as it can kill harmful pathogens like bacteria, viruses, and fungi. Some studies also suggest that lauric acid could be beneficial for heart health, although more research is needed in this area.

The Lauric acid can be retained and analyzed using a mixed-mode Newcrom BH, 4.6 x 150 mm, 5 µm, 100 A column. The mobile phase for this method consists of water, acetonitrile (MeCN), and Ammonium formate, which serves as a buffer. This analytical method can be detected with an Evaporative Light Scattering Detector (ELSD) or any other evaporative detection method (CAD, ESI-MS).

High Performance Liquid Chromatography (HPLC) Method for Analysis of Dodecanoic acid (Lauric acid)

Condition

ColumnNewcrom BH, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseGradient MeCN -40-80%, 10 min
BufferAmmonium formate pH 3.0 – 20 mM
Flow Rate1.0 ml/min
DetectionELSD, the nebulizer and evaporator temperatures 50 °C, with a gas flow rate of 1.6 Standard Liters per Minute (SLM)
(MS- compatible mobile phase)

Description

Class of CompoundsAliphatic sulfonic acid
Analyzing CompoundsDodecanoic acid (Lauric acid)

Application Column

Newcrom BH

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Dodecanoic acid (Lauric acid)
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Method for Separation of Hydrotopic, Cationic and Anion Surfactants on Newcrom BH Column

July 10, 2023

HPLC Method for Analysis of Hydrotopic, Cationic and Anion Surfactants on Newcrom BH by SIELC Technologies

Separation type: Liquid Chromatography Mixed-mode

HPLC Method for Separation of Hydrotopic, Cationic and Anion Surfactants

Surfactants, also known as surface-active agents, are compounds that lower the surface tension (or interfacial tension) between two liquids or between a liquid and a solid. Surfactants may act as detergents, wetting agents, emulsifiers, foaming agents, or dispersants.

They are often classified according to the charge of the polar head group:

Anionic Surfactants: These surfactants have a negative charge on their polar head group. Common examples include soap, sodium laureth sulfate, and sodium lauryl sulfate. They are commonly used in detergents and shampoos due to their ability to emulsify oils and hold dirt in suspension, so it can be rinsed away.

Cationic Surfactants: These surfactants have a positive charge on their polar head group. Examples include cetyltrimethylammonium bromide (CTAB) and benzalkonium chloride. These are often used as antiseptics and can also be found in hair conditioners because they reduce static cling.

Nonionic Surfactants: These surfactants have no charge on their polar head group. Examples include alcohol ethoxylates, nonylphenol ethoxylates, and polysorbates. Nonionic surfactants are often used in laundry and dishwasher detergents.

Hydrotropic Surfactants: While not a category of charge like the others, hydrotropic surfactants are a distinct class that promote the solubility of other solutes in water. Sodium xylene sulfonate and sodium cumene sulfonate are examples of hydrotropes.

The selection of a specific type of surfactant depends on the specific application and the properties of the surfactant. Some surfactants can be aggressive and irritating to skin or eyes (like certain anionic surfactants), while others are milder. Similarly, some are better at emulsifying oil or suspending dirt, while others might provide good foaming action or work better in hard water.

All compounds can be retained, separated, and analyzed using a reverse-phase Newcrom BH, 4.6 x 150 mm, 5 µm, 100 A column. The mobile phase for this method consists of water, acetonitrile (MeCN), and Ammonium formate, which serves as a buffer. This analytical method can be detected with an Evaporative Light Scattering Detector (ELSD) or any other evaporative detection method (CAD, ESI-MS).

High Performance Liquid Chromatography (HPLC) Method for Analysis of Benzalkonium chloride, Cetylpyridinium Chloride, 1-Pentanesulfonic acid, Dodecanoic acid (Lauric acid), p-Toluenesulfonic Acid (PTSA), 1-Octanesulfonic acid, Sodium dodecyl sulfate, 1-Ethylpyridinium bromide

Condition

ColumnNewcrom BH, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseGradient MeCN -40-80%, 10 min
BufferAmmonium formate pH 3.0 – 40 mM
Flow Rate1.0 ml/min
DetectionELSD, 50C

Description

Class of CompoundsSurfactants
Analyzing CompoundsBenzalkonium chloride, Cetylpyridinium Chloride, 1-Pentanesulfonic acid, Dodecanoic acid (Lauric acid), p-Toluenesulfonic Acid (PTSA), 1-Octanesulfonic acid, Sodium dodecyl sulfate, 1-Ethylpyridinium bromide

Application Column

Newcrom BH

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
1-Ethylpyridinium bromide
1-Octanesulfonic acid
1-Pentanesulfonic acid
Benzalkonium chloride
Cetylpyridinium Chloride
Dodecanoic acid (Lauric acid)
Sodium dodecyl sulfate
p-Toluenesulfonic Acid (PTSA)

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

Separation of Dodecanoic acid on Newcrom R1 HPLC column

February 16, 2018
Separation of Dodecanoic acid on Newcrom C18 HPLC column

Dodecanoic acid can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains an acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particles columns available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation impurities in preparative separation. It also suitable for pharmacokinetics.

Application Column

Newcrom R1

The Newcrom columns are a family of reverse-phase-based columns. Newcrom A, AH, B, and BH are all mixed-mode columns with either positive or negative ion-pairing groups attached to either short (25 Å) or long (100 Å) ligand chains. Newcrom R1 is a special reverse-phase column with low silanol activity.

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Application Analytes:
Dodecanoic acid (Lauric acid)
The result was obtained by a proprietary SIELC algorithm. It may deviate from the actual experimental data. The experimental data are available upon request. Contact us by e-mail: support@sielc.com or by phone: 847-229-2629.