Niclosamide-sodium |
![]() Last updated: 13/09/2025 |
![]() |
(Not known by any other names) |
|
![]() |
|
A largely obsolete antiparasitic control agent for humans and animals | |
---|---|---|
|
Used for treating tape worm infections. Also used to control aquatic pests (Aquatic snails; Sea lamprey) | |
|
Horses; Ruminants; Cats; Dogs; Sheep; Poultry; Aquatic Situations |
Approval status |
|
Not approved | |
---|---|---|
|
Not approved |
Chemical structure |
|
None | |
---|---|---|
|
C₁₃H₇Cl₂N₂NaO₄ | |
|
C1=CC(=C(C=C1[N+](=O)[O-])Cl)NC(=O)C2=C(C=CC(=C2)Cl)[O-].[Na+] | |
|
- | |
|
DQZCVHZGOQFNDC-UHFFFAOYSA-M | |
|
InChI=1S/C13H8Cl2N2O4.Na/c14-7-1-4-12(18)9(5-7)13(19)16-11-3-2-8(17(20)21)6-10(11)15;/h1-6,18H,(H,16,19);/q;+1/p-1 | |
|
No |
|
![]() |
Common Name | Relationship | Link |
---|---|---|
niclosamide | Parent | ![]() |
General status |
|
Anthelmintic, Antiparasitic, Nematicide | |
---|---|---|
|
Chloronitrophenol molluscidie | |
|
- | |
|
- | |
|
Synthetic | |
|
Respiratory & stomach action. Acts by uncoupling oxidative phosphorylation in the tapeworm | |
|
[DNA, Antagonist], [Oxidative phosphorylation, Uncoupler], [Glucose uptake, Inhibitor] | |
|
40321-86-6 | |
|
No data found | |
|
599 | |
|
- | |
|
25217869 | |
|
No data found | |
|
Antiparasitic products, insecticides & repellents: Anthelmintics | |
|
QP52AG03 | |
|
No | |
|
- | |
|
349.10 | |
|
sodium;4-chloro-2-[(2-chloro-4-nitrophenyl)carbamoyl]phenolate | |
|
sodium;4-chloro-2-[(2-chloro-4-nitrophenyl)carbamoyl]phenolate | |
|
- | |
|
- | |
|
- | |
|
- | |
|
- | |
|
Commercial |
|
|
|||
---|---|---|---|---|
|
- | |||
|
- | |||
|
|
|||
|
|
|||
|
Available in a variety of formulations, including oral boluses and suspensions, for oral administration as a veterinary treatment and as an emulsifiable concentrate for aquatic use. | |||
|
The production of niclosamide-olamine begins with the synthesis of niclosamide, typically via a condensation reaction between 5-chlorosalicylic acid and 2-chloro-4-nitroaniline in the presence of a chlorinating agent such as phosphorus trichloride, often carried out in a solvent like chlorobenzene at elevated temperatures. The resulting niclosamide is then purified through recrystallisation. To form the sodium salt, niclosamide is then reacted with sodium hydroxide in aqueous or alcoholic solution, converting the phenolic hydroxyl group into its sodium salt form. | |||
|
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. |
|
![]() |
|
|
|
|
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
|
- | - | - | |||||||
|
- | - | - | ||||||||
|
|
- | - | - | |||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
- | |||||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
|
- | - | - | |||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- |
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. | ||||||||||
|
- |
Soil adsorption and mobility |
|
|
|
|
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
|
- | - | - | |||||||
|
- | ||||||||||
|
- | ||||||||||
|
|
- | - | - | |||||||
|
- | ||||||||||
|
- | ||||||||||
|
- | ||||||||||
|
- |
Fate indices |
|
|
|
|
||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
- | - | - | ||||||||||||||||||||||||||
|
|
- | - | - | |||||||||||||||||||||||||
|
- | - |
Known metabolites |
None
|
![]() |
Terrestrial ecotoxicology |
|
|
|
|
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
- | - | - | ||||||||
|
|
- | - | - | |||||||
|
- | - | |||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
|
- | - | - | |||||||
|
- | - | - | ||||||||
|
|
- | - | - | |||||||
|
- | - | - | ||||||||
|
|
- | - | - | |||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | ||||||||||
|
|
- | - | - | |||||||
- | |||||||||||
|
- | - | - | ||||||||
- | |||||||||||
|
|
- | - | - | |||||||
|
- | - | - | ||||||||
|
|
- | - | - | |||||||
|
- | ||||||||||
|
|
- | - | - | |||||||
|
- | ||||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - |
Aquatic ecotoxicology |
|
|
|
|
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
|
- | - | - |
|
- | - | - | |||
|
- | - | - |
|
![]() |
General |
|
|
|
|
||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
|
High (class III) | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
- | - | - | ||||||||
|
|
- | |||||||||
|
May be absorbed through the skin or mucous membranes | ||||||||||
|
Some metabolism, metaboliteand unchanged parent lost mainly via the faeces | L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
- |
Health issues |
|
|
||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
May cause gastrointestinal problems, anorexia, irritability & alopecia Salts may cause occular irritation Harmful if swallowed |
Handling issues |
|
|
|||
---|---|---|---|---|
|
Avoid formation of dust IMDG Transport Hazard Class 9 |
|||
|
- | |||
|
U (Unlikely to present an acute hazard) | |||
|
UN3077 | |||
|
Packaging Group III (minor danger) | |||
|
- |
|
![]() |
|
|
||
---|---|---|---|
|
niclosamide-sodium | ||
|
- | ||
|
- | ||
|
- | ||
|
- | ||
|
- | ||
|
- | ||
|
- | ||
|
- | ||
|
- | ||
|
- | ||
|
- |
Record last updated: | 13/09/2025 |
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 |