Levamisole hydrochloride

Levamisole hydrochloride	Last updated: 14/09/2025
(Not known by any other names)

GENERAL INFORMATION

Description

A veterinary antiparasitic drug of the imidazothiazole class which is usually used as the hydrochloride salt

Examples of veterinary uses

Used mainly as a dewormer in livestock and for freshwater tropical fish

Examples of species treated

Cattle; Pigs; Sheep; Freshwater tropical fish; Elephants

Approval status

VMR 2013/2033 approval status (GB/UK)

Approved - usually avaiable as a prescription only medicine to be authorised by suitably qualified person (POM-VPS)

EU Regulatory approval status

Approved

Chemical structure

Isomerism

Levamisole hydrochloride exhibits chiral isomerism, stemming from a single stereocentre at the 6-position of its imidazothiazole ring system. This chiral centre gives rise to two enantiomers: levamisole (S-enantiomer) and dextramisole (R-enantiomer). Only the S-enantiomer, levamisole, possesses potent anthelmintic and immunomodulatory properties, while the R-form is largely inactive. Tetramisole is the name for the racemic mixture, meaning it contains both the (R)- and (S)-enantiomers of the compound.

Chemical formula

C₁₁H₁₃ClN₂S

Canonical SMILES

C1CSC2=NC(CN21)C3=CC=CC=C3.Cl

Isomeric SMILES

C1CSC2=N[C@H](CN21)C3=CC=CC=C3.Cl

International Chemical Identifier key (InChIKey)

LAZPBGZRMVRFKY-HNCPQSOCSA-N

International Chemical Identifier (InChI)

InChI=1S/C11H12N2S.ClH/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10;/h1-5,10H,6-8H2;1H/t10-;/m1./s1

2D structure diagram/image available?

Yes

Cambridge Crystallographic Data Centre diagrams

Common Name	Relationship	Link
levamisole hydrochloride	-
levamisole	Parent

General status

Veterinary substance type

Dewormer, Antiparasitic, Anthelmintic

Substance groups

Imidazothiazole

Minimum active substance purity

Known relevant impurities

Substance origin

Synthetic

Mode of action

Works by causing parasitic paralysis allowing it to be expelled. Nicotinic receptor agonist.

Molecular targets

[Neuronal acetylcholine receptor subunit alpha-3, Agonist], [Alkaline phosphatase, placental-like, Antagonist]

CAS RN

16595-80-5

Alternative/old CAS RN

39170-95-1

EC number

240-654-6

CIPAC number

US EPA chemical code

PubChem CID

27944

Therapeutic Class

Antiparasitic products, insecticides & repellents: Anthelmintics

ATCvet Code

QP52AE01

Controlled Drug?

Regulation 37/2010 MRL Classification

Allowed substance (Table 1: Bovine, Ovine, Porcine, Poultry)

Molecular mass

240.75

PIN (Preferred Identification Name)

IUPAC name

(6S)-6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole;hydrochloride

CAS name

Forever chemical

Other status information

Relevant Environmental Water Quality Standards

Physical state

Related substances & organisms

tetramisole hydrochloride

levamisole

Commercial

Property

Value

Availability status

Current

Introduction & key dates

1966, discovered

Example manufacturers & suppliers of products using this active now or historically

Chanelle Animal Health Ltd
Elanco Europe Ltd
Norbrook Laboratories Ltd

Example products using this active

Charnaverm Oral Solution
Combinex Oral Solution
Levafas Diamand Oral Suspension

Formulation and application details

Available in a variety of formulations including topically applied solutions, oral solutions and solutions for injection

Commercial production

The production of levamisole hydrochloride typically begins with the synthesis of the imidazothiazole core, often through an aminoalkylation reaction involving precursors like 2-phenylthio-5,6,7,8-tetrahydropyrido[2,1-b][1,3]oxazine, which reacts with anhydrous ammonia under mild conditions to form the desired ring system. Alternatively, some methods start with L-mandelic acid, progressing through steps such as esterification, aminolysis, reduction, chlorination, and ring closure, followed by salification with hydrochloric acid to yield the final salt. Another route involves resolution of racemic tetramisole using dibenzoyl-D-tartaric acid, which selectively precipitates the active S-enantiomer (levamisole), later neutralised and crystallised with hydrochloric acid to form levamisole hydrochloride.

Impact on climate of production and use

Published GHG data is not available for most pharmaceuticals. However, according to industry, global averages suggest producing 1 kg of a typical active pharmaceutical ingredient can range from 10 to 100 kg CO₂e for small molecule drugs and potentially up to 1000 kg CO₂e for complex biologicals such as vaccines, depending on the drug type, its formulation, complexity of synthesis, solvent recovery, and energy sources used.

ENVIRONMENTAL FATE

Property

Value

Source; quality score; and other information

Interpretation

Solubility - In water at 20 °C (mg l⁻¹)

Solubility - In organic solvents at 20 °C (mg l⁻¹)

Melting point (°C)

Boiling point (°C)

Degradation point (°C)

Flashpoint (°C)

Octanol-water partition coefficient at pH 7, 20 °C

Log P

Fat solubility of residues

Solubility

Data type

Density (g ml⁻¹)

Dissociation constant pKa) at 25 °C

Vapour pressure at 20 °C (mPa)

Henry's law constant at 25 °C (Pa m³ mol⁻¹)

Volatilisation as max % of applied dose lost

From plant surface

From soil surface

Maximum UV-vis absorption L mol⁻¹ cm⁻¹

Surface tension (mN m⁻¹)

Refractive Index

Environmental release

Degradation

Property

Value

Source; quality score; and other information

Interpretation

Soil degradation (days) (aerobic)

DT₅₀ (typical)

DT₅₀ (lab at 20 °C)

DT₅₀ (field)

DT₉₀ (lab at 20 °C)

DT₉₀ (field)

Note

Manure DT₅₀ (days)

Aqueous photolysis DT₅₀ (days) at pH 7

Value

Note

Aqueous hydrolysis DT₅₀ (days) at 20 °C and pH 7

Value

Note

Water-sediment DT₅₀ (days)

Water phase only DT₅₀ (days)

Sediment phase only DT₅₀ (days)

Air degradation

As this parameter is not normally measured directly, a surrogate measure is used: ‘Photochemical oxidative DT₅₀’. Where data is available, this can be found in the Fate Indices section below.

Decay in stored produce DT₅₀

Soil adsorption and mobility

Property

Value

Source; quality score; and other information

Interpretation

Linear

K_d (mL g⁻¹)

K_oc (mL g⁻¹)

Notes and range

Freundlich

K_f (mL g⁻¹)

K_foc (mL g⁻¹)

¹/_n

Notes and range

pH sensitivity

Fate indices

Property

Value

Source; quality score; and other information

Interpretation

GUS leaching potential index

Bio-concentration factor

BCF (l kg⁻¹)

CT₅₀ (days)

Known metabolites

None

ECOTOXICOLOGY

Terrestrial ecotoxicology

Property

Value

Source; quality score; and other information

Interpretation

Mammals - Acute oral LD₅₀ (mg kg⁻¹)

180

Rat

Moderate

Mammals - Short term dietary NOEL

(mg kg⁻¹)

(ppm diet)

Mammals - Chronic 21d NOAEL (mg kg⁻¹ bw d⁻¹)

Birds - Acute LD₅₀ (mg kg⁻¹)

Birds - Short term dietary (LC₅₀/LD₅₀)

Birds - Chronic 21d NOEL (mg kg⁻¹ bw d⁻¹)

Earthworms - Acute 14 day LC₅₀ (mg kg⁻¹ dw soil)

Earthworms - Chronic NOEC, reproduction (mg kg⁻¹ dw soil)

Soil micro-organisms

Collembola

Acute LC₅₀ (mg kg⁻¹)

Chronic NOEC (mg kg⁻¹)

Non-target plants

Vegetative vigour ER₅₀ (g ha⁻¹)

Seedling emergence ER₅₀ (g ha⁻¹)

Honeybees (Apis spp.)

Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Unknown mode acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Chronic

Notes

Bumblebees (Bombus spp.)

Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Mason bees (Osmia spp.)

Contact acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Oral acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg bee⁻¹)

Other bee species (1)

Acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg insect⁻¹)

Mode of exposure

Other bee species (2)

Acute LD₅₀ (worst case from 24, 48 and 72 hour values - μg insect⁻¹)

Mode of exposure

Beneficial insects (Ladybirds)

Beneficial insects (Lacewings)

Beneficial insects (Parasitic wasps)

Beneficial insects (Predatory mites)

Beneficial insects (Ground beetles)

Aquatic ecotoxicology

Property

Value

Source; quality score; and other information

Interpretation

Temperate Freshwater Fish - Acute 96 hour LC₅₀ (mg l⁻¹)

Temperate Freshwater Fish - Chronic 21 day NOEC (mg l⁻¹)

Tropical Freshwater Fish - Acute 96 hour LC₅₀ (mg l⁻¹)

Temperate Freshwater Aquatic invertebrates - Acute 48 hour EC₅₀ (mg l⁻¹)

Temperate Freshwater Aquatic invertebrates - Chronic 21 day NOEC (mg l⁻¹)

Tropical Freshwater Aquatic invertebrates - Acute 48 hour EC₅₀ (mg l⁻¹)

Aquatic crustaceans - Acute 96 hour LC₅₀ (mg l⁻¹)

Sediment dwelling organisms - Acute 96 hour LC₅₀ (mg l⁻¹)

Sediment dwelling organisms - Chronic 28 day NOEC, static, water (mg l⁻¹)

Sediment dwelling organisms - Chronic 28 day NOEC, sediment (mg kg⁻¹)

Aquatic Plants (free-floating, fonds growth, fresh) - 7 day (mg l⁻¹)

Aquatic plants (rooted, growth rate, fresh) - 14 day (mg l⁻¹)

Algae - Acute (growth rate, fresh; mg l⁻¹)

Algae - Chronic (growth rate, fresh; mg l⁻¹)

Mesocosm study data

NOEAEC mg l⁻¹

Marine bivalves

HUMAN HEALTH AND PROTECTION

General

Property

Value

Source; quality score; and other information

Interpretation

Threshold of Toxicological Concern (Cramer Class)

High (class III)

Mammals - Acute oral LD₅₀ (mg kg⁻¹)

180

Rat

Moderate

Mammals - Dermal LD₅₀ (mg kg⁻¹ body weight)

Mammals - Inhalation LC₅₀ (mg l⁻¹)

Other Mammal toxicity endpoints

ADI - Acceptable Daily Intake (mg kg⁻¹ bw day⁻¹)

ARfD - Acute Reference Dose (mg kg⁻¹ bw day⁻¹)

AAOEL - Acute Acceptable Operator Exposure Level (mg kg⁻¹ bw day⁻¹)

AOEL - Acceptable Operator Exposure Level - Systemic (mg kg⁻¹ bw day⁻¹)

Dermal penetration studies (%)

Dangerous Substances Directive 76/464

Exposure Routes

Public

Occupational

Mammalian dose elimination route and rate

High level of metabolism, less than 6% excreted unchanged in urine, metabolites excreted in both urine and faeces

Health issues

Specific human health issues (hazard-based)

Carcinogen

Genotoxic

Endocrine disruptor

; ; ; ;

Reproduction / development effects

Acetyl cholinesterase inhibitor

Neurotoxicant

No data found

Respiratory tract irritant

Skin irritant

Skin sensitiser

No data found

Eye irritant

Phototoxicant

No data found

General human health issues

Possible immune system and blood toxicant
May cause stomatitis, nausea, vomiting and adbominal pain

Handling issues

Property

Value and interpretation

General

IMDG Transport Hazard Class 6.1

CLP classification 2013

WHO Classification

Not listed (Not listed)

UN Number

UN2811

Waste disposal & packaging

Packaging Group III (minor danger)

Shelf-life, storage, stability and reactivity

TRANSLATIONS

Language

Name

English

levamisole hydrochloride

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Polish

Swedish

Hungarian

Dutch

Norwegian

Record last updated:	14/09/2025
Contact:	aeru@herts.ac.uk
Please cite as:	Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. (2016) An international database for pesticide risk assessments and management. Human and Ecological Risk Assessment: An International Journal, 22(4), 1050-1064. DOI: 10.1080/10807039.2015.1133242