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Acetylcysteine API from Chinese Manufacturers & Suppliers

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Commercial-scale Suppliers

Distributor
Produced in  Germany
|

Employees: 50+

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

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GMP
CEP
MSDS
BSE/TSE
ISO9001
CoA
Producer
Produced in  Japan
|

Employees: 2400+

|
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

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MSDS
BSE/TSE
ISO9001
CoA
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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
|
CEP
|
USDMF
|
MSDS
|
ISO9001

All certificates

GMP
CEP
USDMF
MSDS
ISO9001
CoA
Producer
Produced in  India
|

Employees: 25

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

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GMP
MSDS
ISO9001
CoA
HALAL
WHO-GMP
Distributor
Produced in  China
|

Employees: 150

|
Audit Report: Click here for more information on Eurofins audit reports
Certifications: USDMF
|
CoA

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USDMF
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

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GMP
MSDS
BSE/TSE
ISO9001
CoA
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Distributor
Produced in  Singapore
|

Employees: 50+

|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: GMP
|
FDA
|
CEP
|
USDMF
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EDMF/ASMF

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

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GMP
MSDS
BSE/TSE
CoA
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Producer
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
|
FDA
|
USDMF
|
ISO9001
|
CoA

All certificates

GMP
FDA
USDMF
ISO9001
CoA
WC
Distributor
Produced in  China
|
Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: coa

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coa
Producer
Produced in  Unknown
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Certifications: FDA
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CEP
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coa

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coa
Producer
Produced in  China
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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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CEP
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KDMF
|
coa

All certificates

GMP
CEP
KDMF
coa
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Producer
Produced in  Japan
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Audit Report: Currently Eurofins has no report for this supplier. Contact them to let them know you're interested!
Certifications: FDA
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CEP
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coa

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FDA
CEP
coa
Producer
Produced in  Spain
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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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CEP
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USDMF
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EDMF/ASMF
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CoA

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EDMF/ASMF
CoA
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Acetylcysteine | CAS No: 616-91-1 | GMP-certified suppliers

A medication that supports respiratory care by reducing thick mucus and provides essential treatment for acetaminophen overdose in key markets such as the US and Canada.

Therapeutic categories

Amino AcidsAmino Acids, NeutralAmino Acids, Peptides, and ProteinsAmino Acids, SulfurAntidote for Acetaminophen OverdoseAntidotes
Generic name
Acetylcysteine
Molecule type
small molecule
CAS number
616-91-1
DrugBank ID
DB06151
Approval status
Approved drug, Investigational drug
ATC code
R05CB01

Primary indications

  • Acetylcysteine is indicated for mucolytic therapy and in the management of [acetaminophen] overdose

Product Snapshot

  • Acetylcysteine is a small‑molecule API available in oral, inhalation, and parenteral formulations
  • It is used for mucolytic applications and for management of acetaminophen toxicity
  • It is approved in the US and Canada, with some investigational listings in additional markets

Clinical Overview

Acetylcysteine (CAS 616-91-1) is an N‑acyl‑L‑alpha‑amino acid used globally as a mucolytic agent and as an established antidote for acetaminophen overdose. Its clinical roles center on reducing mucus viscosity in respiratory conditions and preventing hepatic injury following toxic acetaminophen ingestion. The compound received FDA approval in 1963 and remains widely used across emergency medicine and pulmonary care settings.

The pharmacologic activity in mucolytic therapy arises from reactive sulfhydryl groups that cleave disulfide bonds within mucin glycoproteins. This reduces the size and viscosity of mucin oligomers, improving clearance. Acetylcysteine may also modulate mucin production through antioxidant effects that influence intracellular redox pathways and downstream signaling involved in MUC5AC transcription. Additional antioxidant activity results from deacetylation to cysteine, supporting endogenous glutathione synthesis.

In acetaminophen toxicity, acetylcysteine replenishes glutathione and can directly conjugate the reactive metabolite N‑acetyl‑p‑benzoquinone imine. This prevents accumulation of protein‑bound adducts in hepatocytes that drive necrosis. Timely administration is essential to limit progression of hepatic injury.

Pharmacodynamic characteristics include a short duration of action with dosing intervals that vary by route of administration. The therapeutic window is wide. Key safety considerations include risk of hypersensitivity reactions, gastrointestinal intolerance, and upper gastrointestinal hemorrhage. Taste and odor can affect adherence, and dilution of oral solutions is sometimes used to improve tolerability.

Pharmacokinetic behavior is route dependent. Systemic exposure varies between oral, inhaled, and intravenous administration because of differences in absorption and first‑pass metabolism. The compound is deacetylated to cysteine and undergoes further metabolic pathways before renal elimination.

Acetylcysteine is available in multiple branded and generic products for inhalation, oral, and intravenous use, depending on regional regulatory approvals and clinical context.

For API procurement, sourcing should prioritize verified identity, control of sulfur‑containing impurities, and compliance with pharmacopeial specifications to ensure suitability for sterile or nonsterile finished dosage forms.

Identification & chemistry

Generic name Acetylcysteine
Molecule type Small molecule
CAS 616-91-1
UNII WYQ7N0BPYC
DrugBank ID DB06151

Pharmacology

SummaryAcetylcysteine reduces mucus viscosity by cleaving disulfide bonds in mucin and modulating mucin production through redox‑dependent effects on signaling pathways. It also serves as a cysteine donor for glutathione synthesis, supporting antioxidant defense. In acetaminophen overdose, it conjugates NAPQI directly or replenishes glutathione to facilitate detoxification.
Mechanism of actionA number of possible mechanisms for the mucolytic activity of acetylcysteine have been proposed. Acetylcysteine's sulfhydryl groups may hydrolize disulfide bonds within mucin, breaking down the oligomers, and making the mucin less viscous.Acetylcysteine has also been shown to reduce mucin secretion in rat models.It is an antioxidant in its own right but is also deacetylated to cysteine, which participates in the synthesis of the antioxidant glutathione.The antioxidant activity may also alter intracellular redox reactions, decreasing phosphorylation of EGFR and MAPK, which decrease transcription of the gene MUC5AC which produces mucin. In the case of acetaminophen overdoses, a portion of the drug is metabolized by CYP2E1 to form the potentially toxic metabolite N-acetyl-p-benzoquinone imine (NAPQI).The amount of NAPQI produced in an overdose saturates and depletes glutathione stores.The free NAPQI promiscuously binds to proteins in hepatocytes, leading to cellular necrosis.Acetylcysteine can directly conjugate NAPQI or provide cysteine for glutathione production and NAPQI conjugation.
PharmacodynamicsAcetylcysteine is indicated for mucolytic therapy and in the management of acetaminophen overdose.It has a short duration of action as it is given every 1-8 hours depending on route of administration, and has a wide therapeutic window.Patients should be counselled regarding diluting oral solutions in cola for taste masking,the risk of hypersensitivity, and the risk of upper gastrointestinal hemorrhage.
Targets
TargetOrganismActions
Glutathione synthetaseHumansstimulator
Cystine/glutamate transporterHumansactivator
NAPQI (N-acetyl-p-benzoquinone imine)Humansreducer

ADME / PK

AbsorptionAn 11 g dose in the form of an effervescent tablet for solution reaches a mean C<sub>max</sub> of 26.5 µg/mL, with a T<sub>max</sub> of 2 hours, and an AUC of 186 µg\*h/mL.
Half-lifeThe mean terminal half life of acetylcysteine in adults is 5.6 hoursand in pre-term neonates is 11 hours.
Protein bindingAcetylcysteine is 66-97% protein bound in serum,usually to albumin.
MetabolismAcetylcysteine can be deacetylated by aminoacylase 1 or other undefined deacetylases before undergoing the normal metabolism of cysteine.
Route of eliminationAn oral dose of radiolabelled acetylcysteine is 13-38% recovered in the urine in the first 24 hours,while 3% is recovered in the feces.
Volume of distributionThe volume of distribution of acetylcysteine is 0.47 L/kg.
ClearanceAcetylcysteine has a mean clearance of 0.11 L/hr/kg.

Formulation & handling

  • Highly water‑soluble small molecule suitable for oral, inhalation, and parenteral solutions, with effervescent and soluble tablets leveraging its good aqueous dispersibility.
  • Oxidation‑prone thiol requires protection from air and metal ions during processing and storage, with solutions typically stabilized by controlled pH.
  • IV and inhalation formulations benefit from antioxidant controls and compatible container–closure systems to prevent discoloration and sulfide odor formation.

Regulatory status

LifecycleThe API remains in a protected phase in the US and Canada due to multiple patents extending through 2032, with some earlier protections expiring between 2025 and 2026. Overall, the market is transitioning gradually, with full generic exposure unlikely until the later-expiring patents lapse.
MarketsUS, Canada
Supply Chain
Supply chain summaryMultiple originator and packager companies participate in the manufacturing and distribution of acetylcysteine, indicating a well‑established and diversified supply base. Branded products are marketed primarily in the United States and Canada, reflecting a concentrated but stable regional presence. Several active US patents extend into the mid‑2020s and early 2030s, suggesting that while some competition may already exist for older formulations, later‑expiring patents may continue to limit full generic entry for certain presentations.

Safety

ToxicityPatients experiencing an overdose may present with vomiting, nausea, bronchospasm, periorbital angioedema, and hypotension.Treat patients with symptomatic and supportive measures.Hemodialysis may remove some acetylcysteine from circulation as it is somewhat protein bound.
High Level Warnings:
  • Overexposure is associated with gastrointestinal distress and hypersensitivity‑type reactions, including bronchospasm and localized angioedema
  • High systemic levels may produce cardiovascular depression, such as hypotension
  • Compound shows partial plasma protein binding

Acetylcysteine is a type of Mucolytics


Mucolytics are a vital subcategory of pharmaceutical active pharmaceutical ingredients (APIs) widely used in the treatment of respiratory conditions. Mucolytics are specifically designed to alleviate respiratory distress by enhancing the clearance of mucus from the airways.

These APIs work by breaking down the chemical bonds within mucus, reducing its viscosity and promoting its removal from the respiratory tract. By thinning the mucus, mucolytics facilitate easier expectoration and help to relieve congestion and cough associated with respiratory conditions such as chronic bronchitis, asthma, and cystic fibrosis.

One of the commonly used mucolytics is N-acetylcysteine (NAC), which acts as a precursor for the synthesis of glutathione—a powerful antioxidant. Glutathione helps to protect the respiratory system from oxidative stress and inflammation, promoting healthy lung function. NAC's mucolytic properties make it an effective treatment for conditions characterized by excessive mucus production.

Mucolytics can be formulated in various dosage forms, including oral tablets, effervescent granules, and inhalation solutions. The choice of formulation depends on the target condition and the desired mode of administration.

Overall, mucolytics play a crucial role in the management of respiratory disorders by improving mucus clearance and reducing airway obstruction. These pharmaceutical APIs offer relief to patients suffering from respiratory conditions, promoting better breathing and overall quality of life.


Acetylcysteine (Mucolytics), classified under Respiratory Tract Agents


Respiratory Tract Agents are a vital category of pharmaceutical APIs (Active Pharmaceutical Ingredients) designed to treat respiratory conditions and diseases. These agents are specifically formulated to target the respiratory system, which includes the lungs, airways, and nasal passages. They play a crucial role in managing various respiratory disorders, such as asthma, chronic obstructive pulmonary disease (COPD), and allergic rhinitis.

Respiratory Tract Agents encompass a wide range of medications, including bronchodilators, corticosteroids, antihistamines, and mucolytics. Bronchodilators are commonly used to relieve airway constriction and facilitate smooth breathing by relaxing the muscles in the airways. Corticosteroids help reduce inflammation in the respiratory system, alleviating symptoms and preventing exacerbations. Antihistamines work by blocking histamine receptors, thus mitigating allergic reactions that often impact the respiratory tract. Mucolytics aid in loosening and thinning mucus, making it easier to expel from the airways.

These APIs are developed through rigorous research and development processes, ensuring their efficacy, safety, and compliance with regulatory standards. Pharmaceutical manufacturers rely on advanced technologies and stringent quality control measures to produce high-quality Respiratory Tract Agents. These APIs are subsequently incorporated into various dosage forms, including inhalers, nasal sprays, nebulizers, and oral medications.

Respiratory Tract Agents are essential in the management of respiratory conditions, providing relief from symptoms, improving lung function, and enhancing the overall quality of life for patients. They are prescribed by healthcare professionals and often used in combination therapies to achieve optimal results. As respiratory disorders continue to affect a significant portion of the global population, the development and availability of effective Respiratory Tract Agents play a vital role in addressing these health challenges and improving patient outcomes.



Acetylcysteine API manufacturers & distributors

Compare qualified Acetylcysteine API suppliers worldwide. We currently have 14 companies offering Acetylcysteine API, with manufacturing taking place in 7 different countries. Use the table below to review supplier type, countries of origin, certifications, product portfolio and GMP audit availability.

SupplierTypeCountryProduct originCertificationsPortfolio
Distributor
Singapore Singapore BSE/TSE, CEP, CoA, EDMF/ASMF, FDA, GMP, ISO9001, JDMF, KDMF, MSDS, USDMF, WC200 products
Producer
Germany Unknown CEP, CoA, FDA25 products
Distributor
Germany Unknown BSE/TSE, CoA, GMP, ISO9001, MSDS211 products
Producer
China China BSE/TSE, CoA, GMP, MSDS235 products
Distributor
Denmark China CoA, USDMF252 products
Distributor
Netherlands Germany BSE/TSE, CEP, CoA, GMP, ISO9001, MSDS170 products
Producer
Japan Japan BSE/TSE, CoA, GMP, ISO9001, MSDS55 products
Producer
India India CoA, GMP, HALAL, ISO9001, MSDS, WHO-GMP10 products
Producer
Spain Spain CEP, CoA, EDMF/ASMF, GMP, USDMF50 products
Producer
Japan Japan CEP, CoA, FDA3 products
Producer
China China CoA, FDA, GMP, ISO9001, USDMF, WC4 products
Distributor
China China CEP, CoA, GMP, ISO9001, MSDS, USDMF767 products
Distributor
China China CoA12 products
Producer
China China CEP, CoA, GMP, KDMF2 products

When sending a request, specify which Acetylcysteine 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 Acetylcysteine 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 Acetylcysteine API


Sourcing

What matters most when sourcing GMP-grade Acetylcysteine?
Key considerations include confirming GMP compliance and alignment with US and Canadian regulatory requirements. A diversified manufacturing and packaging base supports supply stability, but product selection may be influenced by active US patents that limit full generic availability for certain presentations. Ensuring that the sourced material fits within these patent and regional constraints is essential.
Which documents are typically required when sourcing Acetylcysteine API?
Request the core API documentation set: CoA (14 companies), GMP (10 companies), MSDS (7 companies), CEP (7 companies), ISO9001 (7 companies). Confirm versions and validity dates match the destination market to avoid delays in qualification.
Which manufacturers are known to produce Acetylcysteine API?
Known or reported manufacturers for Acetylcysteine: Duchefa Farma B.V., Caesar & Loretz GmbH (CAELO), Fujifilm Wako Pure Chemical Corporation, Sinoway industrial Co.,Ltd, Changzhou Comwin Fine Chemicals Co., Ltd, Chr. Olesen Group, Shanxi Yanghe Pharmaceutical Co., Ltd, Apollo Healthcare Resources (Singapore), Innovative Healthcare. Evaluate their GMP history, scale, and regional coverage before requesting dossiers or allocating demand.
How can I request quotes for Acetylcysteine 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 Acetylcysteine manufacturers?
Audit reports may be requested for Acetylcysteine: 2 GMP audit reports available. Confirm the scope and recency of any audit before relying on it for qualification decisions.
How many suppliers offer Acetylcysteine API on Pharmaoffer?
Reported supplier count for Acetylcysteine: 14 verified suppliers. Filter listings by certifications, regions, and delivery options to match your qualification plan.
Which countries are known to manufacture Acetylcysteine API?
Production countries reported for Acetylcysteine: China (6 producers), Japan (2 producers), Germany (1 producer). Knowing the manufacturing geography helps anticipate logistics lead times and import compliance needs.
Which certifications do suppliers of Acetylcysteine usually hold?
Common certifications for Acetylcysteine suppliers: CoA (14 companies), GMP (10 companies), MSDS (7 companies), CEP (7 companies), ISO9001 (7 companies). Always verify issuing authorities and expiry dates when reviewing audit packages.

Technical

What is Acetylcysteine (CAS 616-91-1) used for?
Acetylcysteine is used as a mucolytic agent to reduce mucus viscosity in respiratory conditions by breaking disulfide bonds within mucin. It is also an established antidote for acetaminophen overdose, where it replenishes glutathione and conjugates the toxic metabolite NAPQI to limit hepatic injury.
Which therapeutic class does Acetylcysteine fall into?
Acetylcysteine belongs to the following therapeutic categories: Amino Acids, Amino Acids, Neutral, Amino Acids, Peptides, and Proteins, Amino Acids, Sulfur, Antidote for Acetaminophen Overdose. This positioning helps teams compare alternative APIs, anticipate pharmacology expectations, and align early research priorities.
What conditions is Acetylcysteine mainly prescribed for?
The primary indications for Acetylcysteine: Acetylcysteine is indicated for mucolytic therapy and in the management of [acetaminophen] overdose. These use cases frame the target patient populations and help prioritize formulation and safety evaluations.
How does Acetylcysteine work?
A number of possible mechanisms for the mucolytic activity of Acetylcysteine have been proposed. Acetylcysteine's sulfhydryl groups may hydrolize disulfide bonds within mucin, breaking down the oligomers, and making the mucin less viscous.Acetylcysteine has also been shown to reduce mucin secretion in rat models.It is an antioxidant in its own right but is also deacetylated to cysteine, which participates in the synthesis of the antioxidant glutathione.The antioxidant activity may also alter intracellular redox reactions, decreasing phosphorylation of EGFR and MAPK, which decrease transcription of the gene MUC5AC which produces mucin. In the case of acetaminophen overdoses, a portion of the drug is metabolized by CYP2E1 to form the potentially toxic metabolite N-acetyl-p-benzoquinone imine (NAPQI).The amount of NAPQI produced in an overdose saturates and depletes glutathione stores.The free NAPQI promiscuously binds to proteins in hepatocytes, leading to cellular necrosis.Acetylcysteine can directly conjugate NAPQI or provide cysteine for glutathione production and NAPQI conjugation.
What should someone know about the safety or toxicity profile of Acetylcysteine?
Acetylcysteine has a wide therapeutic window, but excessive exposure can cause gastrointestinal discomfort and hypersensitivity reactions, including bronchospasm and localized angioedema. High systemic levels may lead to cardiovascular depression such as hypotension. Upper gastrointestinal hemorrhage has been reported, and taste or odor of oral solutions can affect tolerability. The compound also shows partial plasma protein binding, with systemic exposure varying by route of administration.
What are important formulation and handling considerations for Acetylcysteine as an API?
Acetylcysteine’s high water solubility supports oral, inhalation, and parenteral solution formulations, and effervescent or soluble tablets use its good aqueous dispersibility. Its thiol group is oxidation‑prone, so processing and storage require protection from air and metal ions and the use of controlled pH to maintain stability. IV and inhalation solutions need antioxidant controls and compatible container–closure systems to limit discoloration and sulfide odor formation.
Is Acetylcysteine a small molecule?
Acetylcysteine is classified as a small molecule. That classification shapes process design, impurity profiling, and analytical control strategies.
Are there special stability concerns for oral Acetylcysteine?
Oral Acetylcysteine is susceptible to oxidation because of its free thiol group, so exposure to air and trace metal ions should be minimized during manufacturing and storage. Formulations are typically protected by maintaining an appropriate pH and using packaging that limits oxygen ingress. Effervescent and soluble tablets also rely on its high aqueous solubility but still require controls to prevent discoloration or sulfide odor formation.

Regulatory

Where is Acetylcysteine approved or in use globally?
Acetylcysteine is reported as approved in the following major regions: US, Canada. Understanding geographic coverage informs regulatory filings, supply planning, and risk assessments before escalating procurement.

Pharmaoffer

How does Pharmaoffer’s Smart Sourcing Service help with Acetylcysteine procurement?
Pharmaoffer's Smart Sourcing Service coordinates compliant suppliers, documentation, and competitive quotes for Acetylcysteine. It centralizes outreach, follow-ups, and document validation to shorten procurement timelines.
Is Acetylcysteine included in the PRO Data Insights coverage?
PRO Data Insights coverage for Acetylcysteine: 919 verified transactions across 287 suppliers and 173 buyers worldwide. Use the dataset to benchmark suppliers and monitor regulatory activity where available.
Where can I access the API market report for Acetylcysteine?
Market report availability for Acetylcysteine: Report Available. The report highlights demand trends, pricing drivers, and supplier landscape insights for procurement planning.