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Moxidectin

CAS No.
113507-06-5
Chemical Name:
Moxidectin
Synonyms
Moxidectin CRS;milbemycin B;Quest;Equest;proheart;Moxetine;Moxdectin;Moxicitin;Moxicodin;Moxicotin
CBNumber:
CB4874771
Molecular Formula:
C37 H53 N O8
Molecular Weight:
639.82
MDL Number:
MFCD00866560
MOL File:
113507-06-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-22 18:57:36
Product description Number Pack Size Price
Moxidectin European Pharmacopoeia (EP) Reference Standard Y0000772 70 mg $175
Moxidectin for system suitability European Pharmacopoeia (EP) Reference Standard Y0000747 10 mg $254
Moxidectin VETRANAL 33746 25mg $218
Moxidectin United States Pharmacopeia (USP) Reference Standard 1448559 200mg $778
Moxidectin M3136 250MG $127
More product size

Moxidectin Properties

Melting point 132 °C
Boiling point 790.0±70.0 °C(Predicted)
Density 1.23±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Store in freezer, under -20°C
solubility ≥128 mg/mL in EtOH; ≥129.4 mg/mL in DMSO; ≥3.27 mg/mL in H2O with gentle warming and ultrasonic
pka 12.46±0.70(Predicted)
form Solid
color White to Almost white
optical activity 139.1°(C=0.01 g/mI, CHCL3 , 20°C, 589nm)
Stability Light Sensitive
InChIKey YZBLFMPOMVTDJY-LSGXYNIPSA-N
SMILES CO\N=C1/C[C@]2(C[C@@H]3CC(C\C=C(C)\C[C@@H](C)\C=C\C=C4/COC5[C@H](O)C(C)=C[C@@H](C(=O)O3)[C@]45O)O2)O[C@@H]([C@H]1C)\C(C)=C\C(C)C
FDA 21 CFR 556.426
FDA UNII NGU5H31YO9
NCI Drug Dictionary moxidectin
ATC code P02CX03
UNSPSC Code 41116107
NACRES NA.77

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS09
Signal word  Danger
Hazard statements  H301-H400
Precautionary statements  P264-P270-P273-P301+P310-P391-P405
Hazard Codes  T,N
Risk Statements  25-50
Safety Statements  45-61-24/25
RIDADR  2588
WGK Germany  3
RTECS  PY5438800
HazardClass  6.1(b)
PackingGroup  III
HS Code  29322090
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Oral
Aquatic Acute 1
NFPA 704
0
4 0

Moxidectin price More Price(42)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0000772 Moxidectin European Pharmacopoeia (EP) Reference Standard 113507-06-5 70 mg $175 2026-04-30 Buy
Sigma-Aldrich Y0000747 Moxidectin for system suitability European Pharmacopoeia (EP) Reference Standard 113507-06-5 10 mg $254 2026-04-30 Buy
Sigma-Aldrich 33746 Moxidectin VETRANAL 113507-06-5 25mg $218 2026-04-30 Buy
Sigma-Aldrich 1448559 Moxidectin United States Pharmacopeia (USP) Reference Standard 113507-06-5 200mg $778 2026-04-30 Buy
TCI Chemical M3136 Moxidectin 113507-06-5 250MG $127 2026-04-30 Buy
Product number Packaging Price Buy
Y0000772 70 mg $175 Buy
Y0000747 10 mg $254 Buy
33746 25mg $218 Buy
1448559 200mg $778 Buy
M3136 250MG $127 Buy

Moxidectin Chemical Properties,Uses,Production

Description

Moxidectin is a macrocyclic lactone endectocide and a derivative of nemadectin. It reduces fecal nematode egg counts by 98.4 and 99.8% in naturally infected calves when administered subcutaneously at doses of 0.2 and 0.3 mg/kg, respectively. Moxidectin (0.2 and 0.3 mg/kg) reduces the worm burden of O. ostertagi and T. axei in the abomasum, and Cooperia species and N. helvetianus in the small intestine, of naturally infected calves. It potentiates GABA-gated currents in Xenopus oocytes expressing rat α1β2γ2 subunit-containing GABAA receptors with an EC50 value of 11.8 nM. Formulations containing moxidectin have been used in the treatment of onchocerciasis, as well as in the prevention and treatment of parasitic infections in veterinary medicine.

Uses

anthelmintic, antiparasitic

Uses

Moxidectin is a semi-synthetic milbemycin derived from nemadectin by selective oxidation followed by methyloximation. Moxidectin was patented in 1991 as an anthelmintic for internal parasite control. The presence of the methyloxime affords moxidectin a greater hydrophobicity and longer biological half-life compared to nemadectin. Moxidectin binds selectively to parasite glutamate-gated chloride ion channels and disrupts neurotransmission leading to paralysis and death of the parasite.

Uses

Moxidectin is a macrocyclic lactone and semisynthetic derivative of nemadectin. Moxidectin is a parasiticide used for the prevention and control of heartworm and intestinal worms. Moxidectin is is fou nd in veterinary medicine used to treat animals such as dogs, cats, horses, cattle and sheep.

Definition

ChEBI: Moxidectin is a milbemycin.

Synthesis

Methoxyamine Hydrochloride

593-56-6

Moxidectin Impurity 13

112124-81-9

Moxidectin

113507-06-5

1. The solid product (0.087 mol) was dissolved in 640 mL of 1,4-dioxane and anhydrous sodium acetate (0.13 mol), acetic acid (0.028 mol) and methoxyamine hydrochloride (0.14 mol) were added sequentially under nitrogen protection. The reaction mixture was stirred at room temperature for 10 hours. The progress of the reaction was monitored by TLC and after confirming the complete reaction of the ingredients, the reaction was terminated by adding 1000 mL of pure water. The reaction mixture was extracted with 1000 mL of ethyl acetate and the extraction was repeated once. The organic phases were combined, dried with anhydrous sodium sulfate and concentrated to give 78.4 g solid. 2. The above solid was dissolved in 4120 mL of ethanol and 1760 mL of pure water was added to adjust the ethanol concentration to 70% (v/v). After filtration to remove insoluble material, 7840 mL of pure water was added for dilution. Extraction was repeated with 13,720 mL of heptane. The heptane layers were combined and concentrated until crystals precipitated, stopping the concentration. Cooled to 20 °C with slow stirring, filtered to separate the crystals and dried under vacuum at 45 °C, -0.08 MPa to give a white solid (0.071 mol). 3. Dissolve the dried crystals (0.071 mol) in 1270 mL of anhydrous methanol and cool to 0 °C. A solution of p-toluenesulfonic acid (0.13 mol) in methanol (120 mL) was added slowly dropwise, keeping the reaction temperature at 0 °C. After dropwise addition, the reaction was continued for 4 h. The reaction progress was monitored by HPLC. The reaction solution was transferred to 2780 mL of saturated sodium bicarbonate solution and washed thoroughly. It was extracted twice with 1270 mL of ethyl acetate, the organic phases were combined, dried over anhydrous sodium sulfate and concentrated to give a solid product (0.054 mol). 4. The resulting solid was dissolved in 23030 mL of 70% (v/v) aqueous methanol and filtered to remove insoluble material. The filtrate was upsampled onto a HP20 macroporous resin column and eluted with 80% (v/v) methanol aqueous solution. The eluate was detected by HPLC and the fraction with 98% purity was collected. Concentrate the eluate to 35% (v/v) methanol and stop the concentration. Cooled to 20°C, stirred slowly for 5 h. The precipitate was withdrawn and dried to give moxidectin (0.015 mol, 96.2% content).

Veterinary Drugs and Treatments

In dogs and cats, moxidectin with lufenuron is indicated as a once a month topical preventative for the prevention of heartworm, flea adulticide, ear mites (cats) and treatment for hookworms, roundworms, and whipworms (dogs). It has also been successfully used as a treatment for generalized demodicosis.
In cattle, moxidectin is indicated for the treatment and control of the following internal [adult and fourth stage larvae (L4)] and external parasites: Gastrointestinal roundworms: Ostertagia ostertagi (adult and L4, including inhibited larvae), Haemonchus placei (adult), Trichostrongylus axei (adult and L4), Trichostrongylus colubriformis (adult), Cooperia oncophora (adult), Cooperia punctata (adult), Bunostomum phlebotomum (adult), Oesophagostomum radiatum (adult), Nematodirus helvetianus (adult); Lungworm: Dictyocaulus viviparus (adult and L4); Cattle Grubs: Hypoderma bovis, Hypoderma lineatum Mites: Chorioptes bovis, Psoroptes ovis (Psoroptes communis var. bovis); Lice: Linognathus vituli, Haematopinus eurysternus, Solenopotes capillatus, Damalinia bovis; Horn flies: Haematobia irritans. To control infections and to protect from reinfection from Ostertagia ostertagi for 28 days after treatment and from Dictyocaulus viviparus for 42 days after treatment.
In sheep, oral moxidectin is indicated for the control of Haemonchus contortus (adult and L4), Teladosrsagia circumcincta & trifurcata (adult and L4), Trichostrongylus colubriformis, axei, & vitrinius (adult & L4), Cooperia curticei & oncophora (adult and L4), Oesophagostomum columbianum & venolosum (adult & L4), and Nematodirus battus, filicollis, & spathiger (adult & L4).
In horses and ponies, moxidectin is indicated for the treatment and control of the following stages of gastrointestinal parasites: Large strongyles: Strongylus vulgaris (adults and L4L5 arterial stages); Strongylus edentatus (adults and tissue stages); Triodontophorus brevicauda (adults); Triodontophorus serratus (adults); Small strongyles (adults and larvae): Cyathostomum spp. (adults); Cylicocyclus spp. (adults); Cylicostephanus spp. (adults); Gyalocephalus capitatus (adults); undifferentiated lumenal larvae; Encysted cyathostomes: late L3 and L4 mucosal cyathostome larvae; Ascarids: Parascaris equorum (adults and L4 larval stages); Pin worms: Oxyuris equi (adults and L4 larval stages); Hair worms: Trichostrongylus axei (adults); Large-mouth stomach worms: Habronema muscae (adults); Horse stomach bots: Gasterophilus intestinalis (2nd and 3rd instars). When combined with praziquantel, additional coverage against Anoplocephala spp. occurs.

References

[1] Tetrahedron Letters, 1988, vol. 29, # 21, p. 2595 - 2598
[2] Patent: CN104017001, 2016, B. Location in patent: Paragraph 0018; 0049; 0050
[3] Patent: CN104277050, 2016, B. Location in patent: Paragraph 0101-0104

112124-81-9
113507-06-5
Synthesis of Moxidectin from Moxidectin Impurity 13

Moxidectin Preparation Products And Raw materials

Global( 422)Suppliers
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View Lastest Price from Moxidectin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Moxidectin pictures 2026-05-02 Moxidectin
113507-06-5
0.99 RongNa Biotechnology Co.,Ltd
Moxidectin pictures 2026-05-01 Moxidectin
113507-06-5
US $0.00 / kg 1kg 98% Customise Hefei Lbao Physical & Chemical Science Co.,Ltd
Moxidectin pictures 2026-04-30 Moxidectin
113507-06-5
US $0.00 / g 100g 99% 100 kg Xi an Biohorlden Industry Trade Co Ltd
  • Moxidectin pictures
  • Moxidectin
    113507-06-5
  • 0.99
  • RongNa Biotechnology Co.,Ltd
  • Moxidectin pictures
  • Moxidectin
    113507-06-5
  • US $0.00 / kg
  • 98%
  • Hefei Lbao Physical & Chemical Science Co.,Ltd
  • Moxidectin pictures
  • Moxidectin
    113507-06-5
  • US $0.00 / g
  • 99%
  • Xi an Biohorlden Industry Trade Co Ltd

Moxidectin Spectrum

(6R,23E,25S)-5-O-DeMethyl-28-deoxy-25-[(1E)-1,3-diMethyl-1-buten-1-yl]-6,28-epoxy-23-(MethoxyiMino)MilbeMycin B [6R,23E,25S(E)]-5-O-DeMethyl-28-deoxy-25-(1,3-diMethyl-1-butenyl)-6,28-epoxy-23-(MethoxyiMino)MilbeMycin B 23-MethoxiMe-LL-F 28249α Equest ProHeart 6 Quest Vetdectin Oral Drench Moxidectin HOUSE STANDARD Moxidectin,MilbeMycin B,23-MethoxiMe-LL-F 28249α,Equest,ProHeart 6 Cydectin, CL 301,423 Moxdectin Milbemycin B, (6R,23E,25S)-5-O-DeMethyl-28-deoxy-25-[(1E)-1,3-diMethyl-1-buten-1-yl]-6,28-epoxy-23-(MethoxyiMino) Moxidectin, >=98% Moxidectin Milbemycin B, 5-O-demethyl-28-deoxy-25-(1E)-1,3-dimethyl-1-butenyl-6,28-epoxy-23-(methoxyimino)-, (6R,23E,25S)- proheart Moxidectin (1448559) MoxidectinQ: What is Moxidectin Q: What is the CAS Number of Moxidectin Q: What is the storage condition of Moxidectin Q: What are the applications of Moxidectin (2R,2a'E,2a1'S,4Z,4'E,5S,6S,6'R,8'E,11'R,15'S,17a'R,20'R,20a'R)-2a1',20'-Dihydroxy-4-(methoxyimino)-5,6',8',19'-tetramethyl-6-((E)-4-methylpent-2-en-2-yl)-2a1',3,4,5,6,6',7',10',11',14',15',17a',20',20a'-tetradecahydro-2'H,17'H-spiro[pyran-2,13'-[11,15]me Anthelmintic and Antiparasitic Drugs Moxidectin (2R,2a'E,2a1'S,4Z,4'E,5S,6S,6'R,8'E,11'R,15'S,17a'R,20'R,20a'R)-2a1',20'-Dihydroxy-4-(methoxyimino)-5,6',8',19'-tetramethyl-6-((E)-4-methylpent-2-en-2-yl)-2a1',3,4,5,6,6',7',10',11',14',15',17a',20',20a'-tetradecahydro-2'H,17'H-spiro[pyran-2,13'-[11,15]methano[1,5]dioxacyclooctadecino[9,8,7-cd]benzofuran]-17'-one Moxidectin Solution in Methanol, 100μg/mL Milbemycin B, 5-O-demethyl-28-deoxy-25-[(1E)-1,3-dimethyl-1-buten-1-yl]-6,28-epoxy-23-(methoxyimino)-, (6R,23E,25S)- (1R,4S,4'E,5'S,6R,6'S,8R,10E,13R,14E,16E,20R,21R,24S)-21,24-dihydroxy-4'-methoxyimino-5',11,13,22-tetramethyl-6'-[(E)-4-methylpent-2-en-2-yl]spiro[3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene-6,2'-oxane]-2-one Moxidectin for system suitability CRS Moxidectin@100 μg/mL in Acetonitrile Moxidectin Solution, 100ppm Milbemycin B,5-O-demethyl-28-deoxy-25-(1,3-dimethyl-1-buten-1-yl)-6,28-epoxy-23-(methoxyimino)-,(6R,23E,25S)- Moxidectin powder CAS 113507-06-5 fiona milbemycin B Moxidectin CRS 113507-06-5 Moxicitin Moxibustin Moxicodin Moxetine Moxicotin Moxidectin in methanol Moxidectin 100 μg/ml Acetonitrile Moxidectin, 10 mM in DMSO Moxidectin - Bio-X ? Moxibustion Moxidexin Moxidectin (CL301423) PharmaVetResiMix 1 Avermectins-v6 10 μg/mL in Methanol D3-Moxidectin (2R,2a'E,2a1'S,4Z,4'E,5S,6S,6'R,8'E,11'R,15'S,17a'R,20'R,20a'R)-2a1',20'-Dihydroxy-4-(methoxyimino)-5,6',8',19'-tetramethyl-6-((E)-4-methylpent-2-en-2-yl)-2a1',3,4,5,6,6',7',10',11',14',15',17a',20',2 113507-06-5 507-06-5 13507-06-5 C37H53NO8 MLSAnalytical Standards Antibiotics BacteriostaticAntibiotics beta-Lactam StructureAlphabetic Chemical Structure Chromatography M