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Triclosan API Manufacturers & Suppliers

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Commercial-scale Suppliers

Distributor
Produced in  China
|

Employees: 50+

|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
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USDMF
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MSDS
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BSE/TSE
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CoA

All certificates

GMP
USDMF
MSDS
BSE/TSE
CoA
Distributor
Produced in  Unknown
|

Employees: 275+

|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
|
MSDS
|
BSE/TSE
|
ISO9001
|
CoA

All certificates

GMP
MSDS
BSE/TSE
ISO9001
CoA
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Producer
Produced in  India
|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
|
USDMF
|
WC
|
CoA

All certificates

GMP
USDMF
WC
CoA
Distributor
Produced in  India
|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: coa

All certificates

coa
Producer
Produced in  Unknown
|
Audit Report: Click here for more information on Eurofins audit reports
Certifications: GMP
|
USDMF
|
CoA

All certificates

GMP
USDMF
CoA
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Triclosan | CAS No: 3380-34-5 | GMP-certified suppliers

A medication that supports broad‑spectrum antimicrobial hygiene in consumer and clinical settings, helping reduce microbial contamination in soaps, oral care products, and healthcare hand scrubs.

Therapeutic categories

Anti-Infective AgentsAnti-Infective Agents, LocalAntiseptics and DisinfectantsBenzene DerivativesDermatologicalsEthers
Generic name
Triclosan
Molecule type
small molecule
CAS number
3380-34-5
DrugBank ID
DB08604
Approval status
Approved drug, Investigational drug
ATC code
D08AE04

Primary indications

  • Triclosan is used in a variety of common household products, including soaps, mouthwashes, dish detergents, toothpastes, deodorants, and hand sanitizers
  • It is also used in health care settings in surgical scrubs and personnel hand washes

Product Snapshot

  • This is a topical and oral-care antimicrobial ingredient supplied in multiple non-sterile formulations such as liquids, gels, soaps, creams, and dentifrices
  • It is used for hygiene and antimicrobial applications in consumer products and healthcare hand-wash or scrub systems
  • It is marketed in the US and Canada with approved uses for certain OTC formulations, while some applications remain investigational

Clinical Overview

Triclosan (CAS 3380-34-5) is a chlorinated diphenyl ether widely used as a broad-spectrum antimicrobial preservative in personal care and household products. It appears in soaps, toothpastes, mouthwashes, deodorants, and hand sanitizers, as well as in health care settings in surgical scrubs and personnel hand washes. Its antimicrobial role is primarily topical and non‑systemic, supporting contamination control in consumer and clinical hygiene applications.

The compound exerts bacteriostatic effects at low concentrations and becomes bactericidal at higher exposures. Its primary biochemical target is the bacterial enoyl‑acyl carrier protein reductase enzyme. By binding ENR and forming a high‑affinity ternary complex with NAD+, triclosan disrupts fatty acid synthesis, compromising cell membrane integrity. Humans lack this enzymatic pathway, which limits direct pharmacological activity in human tissues.

Systemic absorption following topical exposure is generally low but may occur depending on formulation and frequency of use. Absorbed triclosan undergoes hepatic phase II metabolism, predominantly glucuronidation and sulfation, and is eliminated mainly in urine with some fecal excretion. Accumulation is not expected with typical intermittent use, although trace systemic levels have been detected in biomonitoring studies.

Safety considerations include potential skin irritation in sensitive individuals and ongoing evaluation of ecological impact due to environmental persistence. Regulatory authorities in several regions have restricted or phased out specific consumer uses based on risk–benefit assessments, particularly where antimicrobial claims are not essential. Toxicity related to therapeutic exposure is not a clinical concern because triclosan is not used as a systemic drug, but product-specific safety limits apply to over‑the‑counter formulations.

Commercially, triclosan has appeared in various branded hygiene and household products, though market presence has decreased in some jurisdictions following regulatory actions.

For API procurement, sourcing should prioritize compliance with regional restrictions, validated impurity controls, and assurance of manufacturing practices that address potential dioxin‑related contaminants inherent to chlorinated aromatic chemistry.

Identification & chemistry

Generic name Triclosan
Molecule type Small molecule
CAS 3380-34-5
UNII 4NM5039Y5X
DrugBank ID DB08604

Pharmacology

SummaryTriclosan is a broad-spectrum antimicrobial agent that acts primarily by inhibiting the bacterial enoyl‑acyl carrier protein reductase (FabI), blocking fatty acid synthesis essential for cell membrane integrity. At higher concentrations it exhibits biocidal activity through additional cytoplasmic and membrane disruptions. Although it can interact with several human nuclear receptors in vitro, its intended activity is directed at microbial targets.
Mechanism of actionTriclosan is a biocidal compound with multiple targets in the cytoplasm and membrane. At lower concentrations, however, triclosan appears bacteriostatic and is seen to target bacteria mainly by inhibiting fatty acid synthesis. Triclosan binds to enoyl-acyl carrier protein reductase enzyme (ENR). This complex has increased affinity for NAD+ and forms a ternary complex. This complex is unable to participate in fatty acid synthesis, weakening the cell membrane and causing cell death. Humans do not have an ENR enzyme, and thus are not affected.
Targets
TargetOrganismActions
Enoyl-[acyl-carrier-protein] reductase [NADH] FabIEscherichia coli (strain K12)
Enoyl-[acyl-carrier-protein] reductase [NADH]Mycobacterium tuberculosis
Enoyl-[acyl-carrier-protein] reductase [NADH] FabIHelicobacter pylori (strain ATCC 700392 / 26695)

ADME / PK

AbsorptionA study conducted in 2000 demonstrated that low amounts of triclosan can be absorbed through skin and can enter the bloodstream.Triclosan is rapidly absorbed and distributed in the human body.Maximum concentrations are reached within three hours after oral intake. However, the metabolism and excretion of the compound is fast.
Half-lifeThe terminal plasma half life of triclosan is 21 h.
MetabolismTriclosan is prone to phase II metabolism via sulfotransferase and glucuronosyltransferase enzymes (Wang et al., 2004). In humans the resulting conjugates are excreted primarily in urine.
Route of eliminationIn one study, after in vivo topical application of a 64.5mM alcoholic solution of [(3)H]triclosan to rat skin, 12% radioactivity was recovered in the faeces, 8% in the carcass 1% in the urine, 30% in the stratum corneum and 26% was rinsed from the skin surface at 24 hours after application.

Formulation & handling

  • Triclosan is a small-molecule antimicrobial used primarily in topical and oral‑care formulations, with negligible aqueous solubility requiring solubilizers or surfactant systems for liquid products.
  • High logP supports incorporation into emulsions, gels, soaps, and surfactant-rich systems; crystalline solid API may need micronization or melting/dispersing steps for uniform distribution.
  • Stable under typical formulation conditions but sensitive to photodegradation and oxidation, so protect from strong UV and formulate with appropriate antioxidants and opaque packaging when needed.

Regulatory status

LifecyclePatent protection in the US and Canada has lapsed or is approaching expiry, indicating that the API is moving into a post‑exclusivity phase. Both markets are therefore characterized by a mature competitive environment with increasing availability of generics.
MarketsCanada, US
Supply Chain
Supply chain summaryTriclosan is an established antimicrobial ingredient supplied by multiple manufacturers, with no single originator company dominating its production. Branded and private‑label formulations are widely available in North American markets such as the US and Canada. Patent protections have long expired, so the supply landscape consists of mature, fully generic competition.

Safety

ToxicityOral LD50, Rat: 3700 mg/kg; Dermal LD50, Rabbit: 9300 mg/kg
High Level Warnings:
  • Low acute toxicity by oral and dermal routes (oral LD50, rat: ~3700 mg/kg
  • Dermal LD50, rabbit: ~9300 mg/kg), but handling protocols should account for potential irritation at higher exposures
  • May cause skin or eye irritation

Good Manufacturing Practices

Active pharmaceutical ingredients are made in GMP-certified manufacturing facilities. GMP stands for Good Manufacturing Practices and is the main standard in the pharmaceutical industry. cGMP or Current GMP means that the company complies with the most recent requirements/version of GMP. The WHO has its own guideline for GMP, the World Health Organization or WHO GMP. The authority that has audited the company can also be from a country like China (Chinese GMP) or from the EU (EU GMP), every authority has different GMP requirements.
 

Triclosan is a type of Disinfectants


Disinfectants are a crucial subcategory of pharmaceutical Active Pharmaceutical Ingredients (APIs) that play a vital role in maintaining cleanliness and preventing the spread of harmful microorganisms. These chemical agents are designed to eliminate or inhibit the growth of bacteria, viruses, fungi, and other pathogens on various surfaces and objects.

Pharmaceutical-grade disinfectants are formulated to meet stringent quality standards and are commonly used in hospitals, laboratories, pharmaceutical manufacturing facilities, and other healthcare settings. They are also utilized in the food and beverage industry, as well as in households, to ensure proper sanitation and hygiene.

Disinfectants typically contain active ingredients such as quaternary ammonium compounds, chlorine compounds, hydrogen peroxide, or alcohol, which have been proven effective against a broad spectrum of microorganisms. These active ingredients work by disrupting the cell membranes or enzymatic processes of the pathogens, rendering them incapable of replication and causing their eventual destruction.

When selecting a disinfectant, factors such as the intended application, target microorganisms, and compatibility with the surfaces or objects being treated need to be considered. It is crucial to follow proper usage instructions and adhere to recommended contact times for effective disinfection.

In conclusion, disinfectants are essential pharmaceutical APIs used to control and prevent the spread of harmful microorganisms. Their efficacy in eliminating pathogens makes them indispensable in maintaining cleanliness and ensuring public health and safety.


Triclosan (Disinfectants), classified under Antidotes, Deterrents, and Toxicologic Agents


Antidotes, Deterrents, and Toxicologic Agents are an important category of pharmaceutical Active Pharmaceutical Ingredients (APIs) that play a critical role in healthcare and toxicology. These substances are designed to counteract the effects of poisons, toxins, and overdoses, thereby saving lives and preventing severe health consequences.

Antidotes are substances that neutralize the toxic effects of certain drugs, chemicals, or poisons. They work by either directly binding to the toxic substance or by blocking its harmful actions on the body. Antidotes are administered in emergency situations to quickly reverse the effects of poisoning and restore normal physiological functions.

Deterrents, on the other hand, are pharmaceutical agents used to discourage or prevent harmful behaviors, such as substance abuse. They are designed to make the ingestion or misuse of certain substances unpleasant or less desirable. Deterrents can be formulated to cause unpleasant side effects, such as nausea or vomiting, when a particular substance is consumed in excessive amounts.

Toxicologic agents encompass a broad range of pharmaceutical APIs used in toxicology studies and research. These substances are employed to investigate the toxicity, metabolism, and mechanisms of action of various chemicals and compounds. Toxicologic agents are vital for understanding the potential hazards and risks associated with certain substances, ensuring the safety of drugs, and developing effective treatments for poisoning cases.

In conclusion, Antidotes, Deterrents, and Toxicologic Agents are essential categories of pharmaceutical APIs that address poisoning emergencies, deter harmful behaviors, and enable toxicological research. Their development and availability are crucial for safeguarding public health, enhancing patient care, and advancing our understanding of toxicology.



Triclosan API manufacturers & distributors

Compare qualified Triclosan API suppliers worldwide. We currently have 5 companies offering Triclosan API, with manufacturing taking place in 3 different countries. Use the table below to review supplier type, countries of origin, certifications, product portfolio and GMP audit availability.

SupplierTypeCountryProduct originCertificationsPortfolio
Producer
Germany Unknown CoA, GMP, USDMF18 products
Distributor
Germany Unknown BSE/TSE, CoA, GMP, ISO9001, MSDS211 products
Producer
India India CoA, GMP, USDMF, WC3 products
Distributor
United States China BSE/TSE, CoA, GMP, MSDS, USDMF166 products
Distributor
India India CoA70 products

When sending a request, specify which Triclosan API quality you need: for example EP (Ph. Eur.), USP, JP, BP, or another pharmacopoeial standard, as well as the required grade (base, salt, micronised, specific purity, etc.).

Use the list above to find high-quality Triclosan API suppliers. For example, you can select GMP, FDA or ISO certified suppliers. Visit our help page to learn more about sourcing APIs via Pharmaoffer.

Frequently asked questions about Triclosan API


Sourcing

What matters most when sourcing GMP-grade Triclosan?
Key considerations include confirming that the manufacturer complies with GMP standards and meets applicable regulatory expectations in the US and Canada. Documentation should support quality, consistency, and traceability across batches. Because Triclosan is fully generic with multiple suppliers, assessing supply reliability and equivalence of quality systems across manufacturers is also important.
Which documents are typically required when sourcing Triclosan API?
Request the core API documentation set: CoA (5 companies), GMP (4 companies), USDMF (3 companies), MSDS (2 companies), BSE/TSE (2 companies). Confirm versions and validity dates match the destination market to avoid delays in qualification.
Which manufacturers are known to produce Triclosan API?
Known or reported manufacturers for Triclosan: Caesar & Loretz GmbH (CAELO), Pharm Rx Chemical Corp. Evaluate their GMP history, scale, and regional coverage before requesting dossiers or allocating demand.
How can I request quotes for Triclosan API from GMP suppliers?
Submit quote requests through the supplier listings with your specs and required documents (specifications, target volume, delivery timeline, and destination). Providing consistent details upfront speeds comparable offers and clarifies technical feasibility.
Is a GMP audit report available for Triclosan manufacturers?
Audit reports may be requested for Triclosan: 1 GMP audit report available. Confirm the scope and recency of any audit before relying on it for qualification decisions.
How many suppliers offer Triclosan API on Pharmaoffer?
Reported supplier count for Triclosan: 5 verified suppliers. Filter listings by certifications, regions, and delivery options to match your qualification plan.
Which countries are known to manufacture Triclosan API?
Production countries reported for Triclosan: India (2 producers), China (1 producer). Knowing the manufacturing geography helps anticipate logistics lead times and import compliance needs.
Which certifications do suppliers of Triclosan usually hold?
Common certifications for Triclosan suppliers: CoA (5 companies), GMP (4 companies), USDMF (3 companies), MSDS (2 companies), BSE/TSE (2 companies). Always verify issuing authorities and expiry dates when reviewing audit packages.

Technical

What is Triclosan (CAS 3380-34-5) used for?
Triclosan is used as a topical antimicrobial preservative in personal care, household, and health care hygiene products such as soaps, toothpastes, mouthwashes, deodorants, hand sanitizers, surgical scrubs, and personnel hand washes. It provides broad‑spectrum contamination control by inhibiting bacterial enoyl‑ACP reductase and disrupting fatty acid synthesis. Its use is limited to non‑systemic applications, and certain consumer uses are restricted in some regions.
Which therapeutic class does Triclosan fall into?
Triclosan belongs to the following therapeutic categories: Anti-Infective Agents, Anti-Infective Agents, Local, Antiseptics and Disinfectants, Benzene Derivatives, Dermatologicals. This positioning helps teams compare alternative APIs, anticipate pharmacology expectations, and align early research priorities.
What conditions is Triclosan mainly prescribed for?
The primary indications for Triclosan: Triclosan is used in a variety of common household products, including soaps, mouthwashes, dish detergents, toothpastes, deodorants, and hand sanitizers, It is also used in health care settings in surgical scrubs and personnel hand washes. These use cases frame the target patient populations and help prioritize formulation and safety evaluations.
How does Triclosan work?
Triclosan is a biocidal compound with multiple targets in the cytoplasm and membrane. At lower concentrations, however, Triclosan appears bacteriostatic and is seen to target bacteria mainly by inhibiting fatty acid synthesis. Triclosan binds to enoyl-acyl carrier protein reductase enzyme (ENR). This complex has increased affinity for NAD+ and forms a ternary complex. This complex is unable to participate in fatty acid synthesis, weakening the cell membrane and causing cell death. Humans do not have an ENR enzyme, and thus are not affected.
What should someone know about the safety or toxicity profile of Triclosan?
Triclosan has low acute toxicity by oral and dermal routes, but it can cause skin or eye irritation, particularly at higher exposures. Systemic absorption from topical use is generally low, with rapid metabolism and elimination, and accumulation is not expected. Safety considerations focus on local irritation potential, environmental persistence, and adherence to product‑specific regulatory limits. Proper handling should also account for impurity control requirements associated with chlorinated aromatic compounds.
What are important formulation and handling considerations for Triclosan as an API?
Triclosan has negligible aqueous solubility, so liquid formulations typically require solubilizers, surfactants, or emulsion systems, and the crystalline API may need micronization or controlled melting to achieve uniform dispersion. Its high logP supports incorporation into emulsions, gels, soaps, and other surfactant‑rich matrices. The compound is stable under common formulation conditions but is sensitive to photodegradation and oxidation, warranting protection from strong UV light, use of suitable antioxidants, and opaque packaging.
Is Triclosan a small molecule?
Triclosan is classified as a small molecule. That classification shapes process design, impurity profiling, and analytical control strategies.
Are there special stability concerns for oral Triclosan?
Oral Triclosan products require attention to its negligible aqueous solubility, often needing solubilizers or surfactant systems to maintain uniform dispersion. The API is sensitive to photodegradation and oxidation, so formulations should minimize light exposure and may include antioxidants and opaque packaging. Its crystalline nature may also necessitate micronization or controlled dispersion steps to ensure consistent dosing in solid or semi‑solid oral‑care formats.

Regulatory

Where is Triclosan approved or in use globally?
Triclosan is reported as approved in the following major regions: Canada, US. Understanding geographic coverage informs regulatory filings, supply planning, and risk assessments before escalating procurement.
What’s the regulatory and patent landscape for Triclosan right now?
In the United States, Triclosan is not allowed in over‑the‑counter consumer antiseptic washes, and its use in other products is subject to FDA and EPA oversight depending on the product type. In Canada, Triclosan is permitted with concentration limits and environmental risk–management measures. Triclosan’s original patents have long expired, and it is generally considered off‑patent.

Pharmaoffer

How does Pharmaoffer’s Smart Sourcing Service help with Triclosan procurement?
Pharmaoffer's Smart Sourcing Service coordinates compliant suppliers, documentation, and competitive quotes for Triclosan. It centralizes outreach, follow-ups, and document validation to shorten procurement timelines.
Is Triclosan included in the PRO Data Insights coverage?
PRO Data Insights coverage for Triclosan: 2050 verified transactions across 550 suppliers and 289 buyers worldwide. Use the dataset to benchmark suppliers and monitor regulatory activity where available.
Where can I access the API market report for Triclosan?
Market report availability for Triclosan: Report Available. The report highlights demand trends, pricing drivers, and supplier landscape insights for procurement planning.