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ChemicalBook >> CAS DataBase List >>Oxfendazole

Oxfendazole

CAS No.
53716-50-0
Chemical Name:
Oxfendazole
Synonyms
Ox;ofdz;CFDZ;OREX;Hcrt1;PPORX;NRCLP1;LODITAC;hoe8105;rs-8858
CBNumber:
CB4105143
Molecular Formula:
C15H13N3O3S
Molecular Weight:
315.35
MDL Number:
MFCD00801063
MOL File:
53716-50-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-24 18:39:39
Product description Number Pack Size Price
Oxfendazole European Pharmacopoeia (EP) Reference Standard O0225800 50 mg $175
Oxfendazole United States Pharmacopeia (USP) Reference Standard 1483301 200mg $501
Oxfendazole European Pharmacopoeia (EP) Reference Standard O0225800 o0225800 $153
Oxfendazole >98.0%(HPLC)(N) O0391 1g $50
Oxfendazole >98.0%(HPLC)(N) O0391 5g $149
More product size

Oxfendazole Properties

Melting point 298-300C
Density 1.3229 (rough estimate)
refractive index 1.6740 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility DMF: slightly soluble; DMSO: 1 mg/ml; DMSO:PBS (pH 7.2) (1:4): 0.20 mg/ml
form Solid
pka 10.27±0.10(Predicted)
color Crystals from chloroform-methanol
Merck 14,6935
Major Application forensics and toxicology
pharmaceutical (small molecule)
InChI InChI=1S/C15H13N3O3S/c1-21-15(19)18-14-16-12-8-7-11(9-13(12)17-14)22(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)
InChIKey BEZZFPOZAYTVHN-UHFFFAOYSA-N
SMILES C(OC)(=O)NC1NC2=CC(S(C3=CC=CC=C3)=O)=CC=C2N=1
CAS DataBase Reference 53716-50-0(CAS DataBase Reference)
FDA 21 CFR 556.495
FDA UNII OMP2H17F9E
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Health Hazard (GHS08)Environment (GHS09)
GHS08,GHS09
Signal word  Danger
Hazard statements  H360D-H373-H410
Precautionary statements  P202-P260-P273-P280-P308+P313-P391
PPE Eyeshields, Gloves, type N95 (US)
Risk Statements  36
Safety Statements  26
WGK Germany  3
RTECS  FD0835000
HS Code  29339900
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Aquatic Acute 1
Aquatic Chronic 1
Repr. 1B
STOT RE 2
Toxicity LD50 in dogs, rats, mice: >1600, >6400, >6400 mg/kg (Averkin)
NFPA 704
0
2 0

Oxfendazole price More Price(80)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich O0225800 Oxfendazole European Pharmacopoeia (EP) Reference Standard 53716-50-0 50 mg $175 2026-04-30 Buy
Sigma-Aldrich 1483301 Oxfendazole United States Pharmacopeia (USP) Reference Standard 53716-50-0 200mg $501 2026-04-30 Buy
Sigma-Aldrich O0225800 Oxfendazole European Pharmacopoeia (EP) Reference Standard 53716-50-0 o0225800 $153 2024-03-01 Buy
TCI Chemical O0391 Oxfendazole >98.0%(HPLC)(N) 53716-50-0 1g $50 2026-04-30 Buy
TCI Chemical O0391 Oxfendazole >98.0%(HPLC)(N) 53716-50-0 5g $149 2026-04-30 Buy
Product number Packaging Price Buy
O0225800 50 mg $175 Buy
1483301 200mg $501 Buy
O0225800 o0225800 $153 Buy
O0391 1g $50 Buy
O0391 5g $149 Buy

Oxfendazole Chemical Properties,Uses,Production

Description

Oxfendazole is a broad spectrum benzimidazole anthelmintic approved for veterinary use. It is effective to protect livestock and poultry from most of the parasites such as roundworms, tapeworms, strongyles and pinworms. The drug is mainly applied in the form of pills, tables, drenches and bolus, etc. especially for horses, goats, cattle, sheep, etc. The drug functions on parasites by binding to tubulin, which is a structural protein of microtubules. In the parasites the blocking of microtubules interferes with the uptake of glucose, which ultimately empties the glycogen reserves. This blocks the whole energy management mechanism of the parasites and eventually leads to death.

References

https://en.wikipedia.org/wiki/Oxfendazole
http://www.vetsfarma.com/poultry3.html
http://parasitipedia.net/index.php? option=com_content&view=article&id=2517&Itemid=2790

Chemical Properties

Of-White Solid

Originator

Autoworm,Coopers

Uses

PAF inhibitor

Uses

A metabolite of Fenbendazole (F246750).

Definition

ChEBI: A member of the class of benzimidazoles that is fenbendazole in which the sulfur has been oxidised to the corresponding sulfoxide.

Manufacturing Process

5.0 g of 2-amino-4-chloro-1-nitrobenzene is added to a solution of sodium phenyl mercaptide, prepared under nitrogen from 2.53 g 57% sodium hydride and 6.2 ml thiophenol in 20 ml dimethylformamide, with a 10 ml dimethylformamide rinse. The mixture is stirred under nitrogen for 3 h at 20°30°C and then diluted with water. The crude product is washed with water and hexane, then recrystallized from methanol, yielding 2-amino-4-phenylthio-1nitrobenzene.
6.0 g of 2-amino-4-phenylthio-1-nitrobenzene is dissolved in 80 ml acetic anhydride and treated with a few drops of sulfuric acid. The mixture is left at 20°-30°C for 2 h then a little sodium acetate added and the solvent removed under vacuum. The residue is treated with water, filtered and recrystallized from methanol yielding 2-acetamido-4-phenylthio-1-nitrobenzene.
7.0 g of 2-acetamido-4-phenylthio-1-nitrobenzene is dissolved in 70 ml chloroform and treated, at -20°C to -15°C, with a solution of 5.0 g 40% peracetic acid in 10 ml methanol. The mixture is allowed to warm slowly to 20°C and stirred for 4 h. The reaction mixture is extracted with sodium bisulfite solution, then sodium bicarbonate solution, dried and evaporated. The residual gum of 2-acetamido-4-phenylsulfinyl-1-nitrobenzene is treated with 20 ml 5 N sodium hydroxide and 40 ml methanol at 20°-25°C for 1 h. Water is then added and essentially pure 2-amino-4-phenyl-sulfinyl-1-nitrobenzene filtered off. Recrystallization may be effected from benzene.
5.4 g of 2-amino-4-phenylsulfinyl-1-nitrobenzene is hydrogenated at 1 atmosphere pressure in 500 ml methanol in the presence of 5.0 g 5% palladized carbon, until the theoretical uptake of hydrogen has occurred. The catalyst is removed by filtration and the filtrate stripped under vacuum. The residue is recrystallized from methanol-benzene, yielding 1,2-diamino-4phenylsulfinylbenzene.
A mixture of 5.5 g of 1,2-diamino-4-phenylsulfinylbenzene, 4.3 g of 1,3-bismethoxycarbonyl-S-methylisothiourea and 1.2 ml acetic acid in 100 ml ethanol and 100 ml water is refluxed for 4 h. The mixture is cooled and essentially pure 6-phenylsulfinyl-2-carbomethoxyaminobenzimidazole filtered off and washed with methanol. Recrystallization may be effected from methanol-chloroform (melting point 253°C, dec.).

brand name

Synanthic Veterinary (Syntex).

Therapeutic Function

Anthelmintic

Safety Profile

Experimental reproductive effects. Human mutation data reported. Whenheated to decomposition it emits toxic fumes of SOx and NOx.

Veterinary Drugs and Treatments

Oxfendazole (Synanthic) is indicated in cattle for the removal and control of lungworms, roundworms (including inhibited forms of Ostertagia ostertagi) and tapeworms.
Oxfendazole as Benzelmin was indicated (no longer marketed in the USA) for the removal of the following parasites in horses: large roundworms (Parascaris equorum), large strongyles (S. edentatus, S. equinus, S. vulgaris), small strongyles, and pinworms (Oxyuris equi).
Oxfendazole has also been used extra-label in sheep, goats, and swine; see Dosage section for more information.

References

[1] Patent: US4792610, 1988, A

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View Lastest Price from Oxfendazole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Oxfendazole pictures 2026-07-30 Oxfendazole
53716-50-0
25KG 97.5%-100.5%;EP 1000KG WUHAN FORTUNA CHEMICAL CO., LTD
Oxfendazole pictures 2026-07-28 Oxfendazole
53716-50-0
1Gram 98% 50KG Hangzhou Hyper Chemicals Limited
Oxfendazole pictures 2026-05-28 Oxfendazole
53716-50-0
$120.70 10KG 99% 10000kg Hebei Chuanghai Biotechnology Co,.LTD
  • Oxfendazole pictures
  • Oxfendazole
    53716-50-0
  • 97.5%-100.5%;EP
  • WUHAN FORTUNA CHEMICAL CO., LTD
  • Oxfendazole pictures
  • Oxfendazole
    53716-50-0
  • 98%
  • Hangzhou Hyper Chemicals Limited
  • Oxfendazole pictures
  • Oxfendazole
    53716-50-0
  • $120.70
  • 99%
  • Hebei Chuanghai Biotechnology Co,.LTD

Oxfendazole Spectrum

[5-(phenylsulfinyl)-1h-benzimidazol-2-yl]carbamic acid methyl ester LODITAC (5-(phenylsulfinyl)-1h-benzimidazol-2-yl)-carbamicacimethylester 5-(phenylsulfinyl)-2-benzimidazolecarbamicacidmethylester 5-(phenylsulfinyl)-2-benzimidazolecarbamicacimethylester 5-phenylsulfinyl-2-carbomethoxyaminobenzimidazole OXFENDAZOLE Oxfendazole BPV98 Oxfendazole, Vetranal OxfendazoleUsp hoe8105 methyl(5-phenylsulfinyl)-1h-benzimidazol-2-ylcarbamate methyl5-(phenylsulfinyl)-2-benzimidazolecarbamate ofdz repidose rs-8858 synanthic systamex CFDZ Oxfendazole Standard Carbamic acid, 5-(phenylsulfinyl)-1H-benzimidazol-2-yl-, methyl ester Carbamic acid, [5-(phenylsulfinyl)-1H-benzimidazol-2-yl]-, methyl ester (9CI) Methyl (5-benzenesulfinyl-2-benzimidazolyl)carbamate Oxfendazole(Fenbendazolesulfoxide) Oxfendazole 0 oxfendazole Solution, 100ppm methyl N-(6-phenylsulfinyl-1H-benzimidazol-2-yl)carbamate N-(6-phenylsulfinyl-1H-benzimidazol-2-yl)carbamic acid methyl ester methyl N-[5-(benzene Oxfendazole (200 mg) Oxfenbendazole Oxphendazole Oxfendazole For Veterinary Use COS Methyl [5-(Phenylsulfinyl)benzimidazol-2-yl]carbamate [5-(Phenylsulfinyl)benzimidazol-2-yl]carbamic Acid Methyl Ester Oxfendazole powder Oxfendazole> Fenbendazole Sulphoxide (Oxfendazol Oxfendazole with impurity D CRS Oxfendazole CRS Carbamic acid, N-[6-(phenylsulfinyl)-1H-benzimidazol-2-yl]-, methyl ester methyl (5-(phenylsulfinyl)-1H-benzo[d]imidazol-2-yl)carbamate Oxfendazole Solution in Methanol, 100μg/mL Methyl [5-(Phenylsulfinyl)benzimidazol-2-yl]carbamate [5-(Phenylsulfinyl)benzimidazol-2-yl]carbamic Acid Methyl Ester Oxfendazole USP/EP/BP Fenbendazole Sulphoxide Oxfendazole (1483301) The command of azole Methyl (6-(phenylsulfinyl)-1H-benzo[d]imidazol-2-yl)carbamate Orfenidazole Oxfendazole, ≥ 98.0% Orfendazole Ovendazole C15783000 Oxfendazole Oxfendazole, 10 mM in DMSO Hcrt1 NRCLP1 OREX
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