Triclosan

Triclosan structural formula

CAS Number3380-34-5
Molecular FormulaC12H7Cl3O2
Molecular Weight289.541
InChI KeyXEFQLINVKFYRCS-UHFFFAOYSA-N
LogP4.76
Synonyms
  • Triclosan
  • 5-Chloro-2-(2,4-dichlorophenoxy)phenol
  • Phenol, 5-chloro-2-(2,4-dichlorophenoxy)-
  • 3380-34-5
  • 5-Chloro-2-(2,4-dichlorophenoxy)phenol
  • Phenol, 5-chloro-2-(2,4-dichlorophenoxy)-
  • 2, 4, 4'-Trichloro-2'-hydroxydiphenylether
  • 2,2'-Oxybis(1',5'-dichlorophenyl-5-chlorophenol)
  • 2,4,4'-TRICHLORO-2'-HYDROXY DIPHENYLETHER
  • 2',4',4-Trichloro-2-hydroxydiphenyl ether
  • 2',4,4'-Trichloro-2-hydroxydiphenyl ether
  • 2,4,4'-Trichloro-2'-hydroxydiphenyl ether
  • 2'-Hydroxy-2,4,4'-trichlorodiphenyl ether
  • 2-Hydroxy-2',4,4'-trichlorodiphenyl ether
  • 3-Chloro-6-(2,4-dichlorophenoxy)phenol
  • 4-Chloro-2-hydroxyphenyl 2,4-dichlorophenyl ether
  • 5-Chloro-2-(2', 4'-dichlorophenoxy) phenol
  • Aquasept
  • Bacti-Stat soap
  • Cansan TCH
  • DIPHENYL ETHER, 2,4,4'-TRICHLORO-2'-HYDROXY-
  • Irgacare MP
  • Irgacide LP 10
  • Irgaguard B 1000
  • Irgaguard B 1325
  • Irgasan
  • Irgasan CH 3565
  • Irgasan DP 30
  • Irgasan DP 300
  • Irgasan DP 3000
  • Irgasan DP 400
  • Irgasan PE 30
  • Irgasan PG 60
  • Microban Additive B
  • Microban B
  • Oletron
  • Phenol, 5-chloro-2-(2,4-dichlorophenoxy)
  • Phenol, 5-chloro-2-(2,4-dichlorophenoxy)-, dihydrogen phosphate
  • Sanitized XTX
  • Sapoderm
  • SterZac
  • Tinosan AM 100
  • Tinosan AM 110
  • TRICLOSAM
  • Ultra Fresh NM 100
  • Ultrafresh NM-V 2
  • Vinyzene DP 7000
  • Yujiexin
  • Zilesan UW
  • BRN 2057142
  • Caswell No. 186A
  • Cloxifenolum
  • EINECS 222-182-2
  • EPA Pesticide Chemical Code 054901
  • Irgasan DP300
  • Phenyl ether, 2'-hydroxy-2,4,4'-trichloro-
  • Triclosanum
  • UNII-4NM5039Y5X
  • Neostrata Antibacterial Facial Cleanser
  • 5-Chloro-2-(2,4-dichloro-phenoxy)-phenol
  • 112099-35-1
  • 1155174-27-8
  • 164325-69-3
  • 261921-78-2
  • 88032-08-0

Applications:

HPLC Method for Analysis of Triclosan on Newcrom R1 Column

September 21, 2023

HPLC Method for Analysis of Triclosan on Newcrom R1 Column by SIELC Technologies

Separation type: Liquid Chromatography Reversed-phase

HPLC Method for Analysis of Triclosan on Newcrom R1 Column
HPLC Method for Analysis of Triclosan on Newcrom R1 Column by SIELC Technologies

Triclosan is an antimicrobial and antifungal agent that has been used in a variety of consumer products, including soaps, toothpastes, deodorants, and cosmetics, as well as in medical devices and textiles. Here are some key points about triclosan:

Mechanism of Action: Triclosan works by inhibiting the synthesis of fatty acids in bacteria, which are essential components of the bacterial cell membrane. Specifically, it targets the enzyme enoyl-acyl carrier protein reductase (ENR).

Controversy and Concerns:

Resistance: There have been concerns that widespread use of triclosan may contribute to antibiotic resistance, as bacteria that become resistant to triclosan might also become resistant to certain antibiotics.
Environmental Concerns: Triclosan is persistent in the environment and has been detected in various water sources. It can be transformed into other chemicals, like dioxins, when exposed to sunlight in aquatic environments.
Health Concerns: Some studies have raised questions about potential endocrine-disrupting effects of triclosan, particularly its impact on thyroid function. Additionally, its potential to contribute to allergic responses, such as skin sensitization, has been discussed.

Triclosan can be retained and analyzed on a mixed-mode Newcrom R1 column with a mobile phase consisting of water, Acetonitrile (MeCN), and sulfuric acid. This analytical method can be detected with high resolution and peak symmetry at a wavelength of 200 nm using UV detection

High Performance Liquid Chromatography (HPLC) Method for Analyses of Triclosan on Newcrom R1 Column by SIELC Technologies

Condition

ColumnNewcrom R1, 4.6 x 150 mm, 3 µm, 100 A
Mobile PhaseMeCN/H2O – 70%,
BufferH2SO4 – 0.2%
Flow Rate1.0 ml/min
DetectionUV 200 nm

Description

Class of CompoundsDiphenyl ethers
Analyzing CompoundsTriclosan

Application Column

Newcrom R1

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 3 µm
Pore Size: 100 A

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Application Analytes:
Triclosan

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.

HPLC Method for Separation of a Mixture of Antifungal Agents on Newcrom R1 Column

September 20, 2023

HPLC Method for Analysis of Antifungal Agents on Newcrom R1 by SIELC Technologies

HPLC Method for Separation of a Mixture of Antifungal Agents on Newcrom R1 Column
HPLC Method for Separation of a Mixture of Antifungal Agents on Newcrom R1 Column


Separation and Analysis of Antifungal Agents on a Newcrom R1 Reverse Phase Column Using Gradient HPLC Method

Antifungal agents are drugs used to treat fungal infections. Depending on their mechanism of action and chemical structure, antifungal agents can be categorized into several classes. Here are some of the main classes and examples of antifungal agents:

  1. Fluconazole: A triazole antifungal mainly used for the treatment and prevention of superficial and systemic fungal infections.
  2. Ketoconazole: An imidazole antifungal used to treat a wide variety of fungal infections, though its oral use has become less common due to potential side effects. It’s still frequently used topically.
  3. Climbazole: An imidazole antifungal primarily used in hair care products to treat dandruff.
  4. Clotrimazole: An imidazole antifungal used to treat various fungal infections including vaginal yeast infections, oral thrush, and ringworm.
  5. Itraconazole: A triazole antifungal used primarily to treat a variety of systemic fungal infections.
  6. Terbinafine: This compound belongs to the allylamine class. It’s mainly used to treat fungal infections of the nails and skin, like athlete’s foot and ringworm.
  7. Econazole: An imidazole antifungal used mainly for skin infections such as athlete’s foot and ringworm.
  8. Miconazole: An imidazole antifungal with a broad spectrum of activity. It’s used for a variety of skin infections and also as a vaginal cream for yeast infections.
  9. Triclosan: This is a broad-spectrum antimicrobial agent. While it has some antifungal activity, it’s more commonly known for its antibacterial properties. Due to concerns regarding its safety and potential contribution to antibiotic resistance, its use in hand soaps and some other personal care products has been phased out in several regions.

Of these, fluconazole, itraconazole, ketoconazole, climbazole, clotrimazole, econazole, and miconazole belong to the azole class, which primarily acts by inhibiting the fungal enzyme lanosterol 14α-demethylase. This enzyme is crucial for ergosterol synthesis, a vital component of fungal cell membranes. Terbinafine, on the other hand, inhibits squalene epoxidase, another enzyme important in ergosterol synthesis. Triclosan works through a different mechanism, targeting bacterial and fungal fatty acid synthesis.

Antifungal agents can be separated, retained, and analyzed on a Newcrom R1 reverse phase column using an gradient analytical method with a simple mobile phase of water, Acetonitrile (MeCN), and sulfuric acid as a buffer. This analysis method can be detected in the UV 200 nm.

ColumnNewcrom R1, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseGradient MeCN – 40-90%, 10 min, hold 2 min
BufferH2SO4 – 0.2%
Flow Rate1.0 ml/min
DetectionUV, 200 nm
Class of Compounds
Antifungal Agents
Analyzing CompoundsFluconazole, Ketoconazole, Climbazole, Clotrimazole, Itraconazole, Terbinafine, Econazole, Miconazole, Triclosan

Application Column

Newcrom R1

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

Add to cart
Application Analytes:
Climbazole
Clotrimazole
Econazole
Fluconazole
Itraconazole
Ketoconazole
Miconazole
Terbinafine
Triclosan

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 Triclosan on Newcrom R1 HPLC column

February 16, 2018
Separation of Triclosan on Newcrom C18 HPLC column

Triclosan 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:
Triclosan
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.