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Furaltadone

Product Name
Furaltadone
CAS No.
139-91-3
Chemical Name
Furaltadone
Synonyms
f-150;nf260;ibifur;unifur;valsyn;altafur;Darifur;otifuril;sepsinol;ultrafur
CBNumber
CB8720393
Molecular Formula
C13H16N4O6
Formula Weight
324.29
MOL File
139-91-3.mol
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Furaltadone Property

Melting point:
206°C (dec.)
Boiling point:
462.63°C (rough estimate)
Density 
1.3046 (rough estimate)
refractive index 
1.6120 (estimate)
storage temp. 
Sealed in dry,2-8°C
solubility 
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
pka
pKa 5.0 (Uncertain)
color 
Yellow
BRN 
8130725
Stability:
Light sensitive
EPA Substance Registry System
Furaltadone (139-91-3)
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Safety

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38
Safety Statements 
3-26
RIDADR 
3249
WGK Germany 
3
RTECS 
RQ3620000
HazardClass 
6.1(b)
PackingGroup 
III
Toxicity
mouse,LD50,intraperitoneal,1gm/kg (1000mg/kg),LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSIONKIDNEY, URETER, AND BLADDER: OTHER CHANGES IN URINE COMPOSITIONBEHAVIORAL: ANTIPSYCHOTIC,Journal of Pharmacy and Pharmacology. Vol. 16, Pg. 663, 1964.
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
F9130
Product name
Furaltadone
Packaging
25g
Price
$70.1
Updated
2024/03/01
Sigma-Aldrich
Product number
46289
Product name
Furaltadone
Purity
VETRANAL
Packaging
250mg
Price
$68
Updated
2024/03/01
TRC
Product number
B497335
Product name
Furaltadone
Packaging
100mg
Price
$70
Updated
2021/12/16
TRC
Product number
B497335
Product name
Furaltadone
Packaging
50mg
Price
$50
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
10456
Product name
Furaltadone
Packaging
10mg
Price
$860
Updated
2021/12/16
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Furaltadone Chemical Properties,Usage,Production

Description

This nitrofuran derivative can be added to animal feed. It induced contact dermatitis in a farm employee.

Chemical Properties

Yellow Crystalline Solid

Originator

Altafur,Norwich Eaton,US,1959

Uses

A metabolite of Nitrofuran in milk. Antibacterial

Uses

Furaltadone is a metabolite of Nitrofuran in milk and an intermediate in the synthesis of AMOZ (A634600), a metabolite of Furaltadone Hydrochloride.

Definition

ChEBI: An oxazolidinone that is 1,3-oxazolidin-2-one substituted at position 1 by a (5-nitro-2-furyl)methylene]amino group and at position 5 by a morpholin-4-ylmethyl group. An antibacterial formerly used oraly but withdrawn due to toxicity, it is used topically as the hydrochloride salt) for treatment of ear disorders.

Manufacturing Process

11.17 g (0.78 mol) 3-(N-morpholinyl)-1,2-epoxypropane, BP 76.5°C to 78°C. 3.9 mm, prepared by Eisleb's method for 3-(1-piperidyl)-1,2-epoxypropane (US Patent 1,790,042) is added dropwise in 12 minutes to 19.5 g (0.39 mol) 100% hydrazine hydrate, which has been warmed to 85% on the steam bath, and is being mechanically stirred. The heat of the reaction maintains the internal temperature at 90°C to 100°C without further external heating. The reaction mixture is then warmed on the steam bath for an additional two hours (90°C to 95°C). The excess hydrazine hydrate is removed in vacuo. The residue of viscous 1-hydrazino-3-morpholinyl-2-propanol is not distilled, but is mixed with 10.16 g (0.086 mol) diethyl carbonate and a solution of 0.3 g sodium metal in 15 ml methyl alcohol. The mixture is refluxed about 2 hours under a 15 cm Widmer column, the alcohol being removed leaving a thick, green liquid residue, which is cooled and the precipitate which forms is removed by filtration and washed well with ether. Yield 82%. MP 114°C to 116°C. Recrystallization from isopropanol gives purified 3-amino-5-(Nmorpholinyl)-methyl-2-oxazolidone, MP 120°C as the intermediate.
It is not necessary that the intermediate be separated from the reaction medium in the preparation of the end product. Instead, the reaction mixture, after cooling, is treated with 200 ml of water acidified with 42 ml 10% hydrochloric acid solution, and filtered. To the clear, light yellow filtrate is added dropwise a solution of 9.8 g (0.07 mol) 5-nitro-2-furaldehyde in 100 ml ethyl alcohol. An orange solution of the hydrochloride results. The free base is precipitated as yellow plates by making the solution basic with saturated sodium carbonate solution. 14 g of the compound is filtered off by suction, washed with alcohol, and dried. The yield, MP 204°C to 205°C (dec.), is 53% of theoretical based on 3-(N-morpholinyl)-1,2-epoxy-propane.
Recrystallization from 95% alcohol (75%recovery) raises the melting point to 206°C (dec.).
The hydrochloride salt is isolated quantitatively by suspending the base in alcohol and adding sufficient aqueous concentrated HCl solution. The precipitate becomes pale yellow, is filtered off, and recrystallized from 80% alcohol. The MP range is about 223°C to 228°C (dec.).

Therapeutic Function

Antibacterial

Contact allergens

This nitrofuran derivative can be added in animal feed or in eardrops

Furaltadone Preparation Products And Raw materials

Raw materials

Preparation Products

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Furaltadone Suppliers

Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Sichuan Kulinan Technology Co., Ltd
Tel
400-1166-196 18981987031
Fax
028-84555506 800101999
Email
cdhxsj@163.com
Country
China
ProdList
11707
Advantage
57
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9815
Advantage
79
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Shanghai Ruji Biology Technology Co., Ltd.
Tel
+86-21-65211385-8001 36031160
Fax
+86-21-65211385-8004
Email
sales@shruji.com
Country
China
ProdList
3224
Advantage
55
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Fax
025-57019371
Email
sales@sunlidabio.com
Country
China
ProdList
3239
Advantage
55
TargetMol Chemicals Inc.
Tel
021-021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7783
Advantage
58
Shanghai TaoSu Biochemical Technology Co., Ltd.
Tel
021-33632979
Fax
021-34692979
Email
info@tsbiochem.com
Country
China
ProdList
8065
Advantage
58
Shanghai BeiZhuo Biotech Co., Ltd.
Tel
021-61119791,13386096464
Fax
021-50190009
Email
bzswkf@foxmail.com
Country
China
ProdList
3921
Advantage
50
Shanghai JONLN Reagent Co., Ltd.
Tel
400-0066400 13621662912
Fax
021-55660885
Email
422131432@qq.com
Country
China
ProdList
9978
Advantage
55
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View Lastest Price from Furaltadone manufacturers

Hebei Weibang Biotechnology Co., Ltd
Product
Furaltadone 139-91-3
Price
US $10.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2021-09-01
Hebei Mojin Biotechnology Co., Ltd
Product
Furaltadone 139-91-3
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
50000KG/month
Release date
2023-08-31
Zhuozhou Wenxi import and Export Co., Ltd
Product
Furaltadone 139-91-3
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-10

139-91-3, FuraltadoneRelated Search:


  • 5-MORPHOLINOMETHYL-3-(5-NITROFURFURYLIDENEAMINO)-2-OXAZOLIDINONE
  • 2-Oxazolidinone, 5-(4-morpholinylmethyl)-3-(5-nitro-2-furanyl)methyleneamino-
  • FURALTADONEBASE
  • 5-(Morpholinomethyl)-3-(((5-nitrofuran-2-yl)methylene)amino)oxazolidin-2-one
  • FURALTADONE VETRANAL
  • FURALTADONE FREE BASE
  • 5-MORPHOLINOMETHYL-3-(5-NITROFURFURYLIDENEAMINO)OXAZOLIDONE
  • Furaltadone (base and/or unspecified salts)
  • 5-(4-Morpholinylmethyl)-3-[[(5-nitro-2-furanyl)methylene]amino]-2-oxazolidinone
  • 5-(Morpholinomethyl)-3-(5-nitrofurfurylidenamino)-2-oxazolidone
  • altafur
  • f-150
  • furazolin
  • furazoline
  • furmethanol
  • furmethonol
  • furmetonol
  • ibifur
  • medifuran
  • nf260
  • nitraldone
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  • nitrofurmeton
  • otifuril
  • sepsinol
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  • FURALTADON
  • FURALTADONE
  • 5-(4-morpholinylmethyl)-3-[(E)-(5-nitro-2-furanyl)methylideneamino]-2-oxazolidinone
  • 5-(4-Morpholinomethyl)-3-(5-nitro-2-furfurylideneamino)-2-oxazolidinone
  • 5-(Morpholinomethyl)-3-[[(5-nitro-2-furyl)methylene]amino]-2-oxazolidinone
  • 2-Oxazolidinone, 5-(morpholinomethyl)-3-[(5-nitrofurfurylidene)amino]-
  • Component of altapen
  • Darifur
  • Furaltadone,5-Morpholinomethyl-3-(5-nitrofurfurylideneamino)-2-oxazolidinone
  • Boschniakia rossica Fedtsch.et Flerov
  • Furaltatone
  • (E)-5-(MorpholinoMethyl)-3-(((5-nitrofuran-2-yl)Methylene)aMino)oxazolidin-2-one
  • Furaltadone h
  • Furaltadone solution, 100ug/ml
  • 5-(morpholinomethyl)-3-((5-nitrofurfurylidene)amino)-2-oxazolidinon
  • 5-morpholinomethyl-3-(5-nitro-2-furfurylidine-amino)-2-oxazolidinone
  • altabactina
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  • Furaltadone Solution in Acetonitrile, 1000μg/mL
  • Furaltadone USP/EP/BP
  • Furan it ketone
  • Acrylamide Impurity 34
  • 139-91-3
  • C13H16N4O6
  • Intermediates & Fine Chemicals
  • Pharmaceuticals