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139-91-3

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139-91-3 Usage

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

Different sources of media describe the Uses of 139-91-3 differently. You can refer to the following data:
1. A metabolite of Nitrofuran in milk. Antibacterial
2. 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 An antibacterial formerly used oraly but withdrawn due to toxicity, it is used topically as the hydrochloride salt) for treatment of ear disorders.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

Check Digit Verification of cas no

The CAS Registry Mumber 139-91-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 139-91:
(5*1)+(4*3)+(3*9)+(2*9)+(1*1)=63
63 % 10 = 3
So 139-91-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H16N4O6/c18-13-16(14-7-10-1-2-12(22-10)17(19)20)9-11(23-13)8-15-3-5-21-6-4-15/h1-2,7,11H,3-6,8-9H2/b14-7+

139-91-3 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Sigma

  • (F9130)  Furaltadone  

  • 139-91-3

  • F9130-25G

  • 556.92CNY

  • Detail
  • Sigma-Aldrich

  • (46289)  Furaltadone  VETRANAL, analytical standard

  • 139-91-3

  • 46289-250MG

  • 299.52CNY

  • Detail

139-91-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name furaltadone

1.2 Other means of identification

Product number -
Other names Darifur

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:139-91-3 SDS

139-91-3Synthetic route

5-nitrofurane-2-carboxaldehyde
698-63-5

5-nitrofurane-2-carboxaldehyde

3-amino-5-(morpholinomethyl)oxazolidin-2-one
43056-63-9

3-amino-5-(morpholinomethyl)oxazolidin-2-one

furaltadone
139-91-3

furaltadone

Conditions
ConditionsYield
With sulfuric acid In propan-1-ol; water
5-nitrofurane-2-carboxaldehyde
698-63-5

5-nitrofurane-2-carboxaldehyde

(+-)-3-amino-5-morpholinomethyl-oxazolidin-2-one

(+-)-3-amino-5-morpholinomethyl-oxazolidin-2-one

furaltadone
139-91-3

furaltadone

Conditions
ConditionsYield
With hydrogenchloride
furaltadone
139-91-3

furaltadone

3-(5-amino-furan-2-ylmethyleneamino)-5-morpholin-4-ylmethyl-oxazolidin-2-one
93429-41-5

3-(5-amino-furan-2-ylmethyleneamino)-5-morpholin-4-ylmethyl-oxazolidin-2-one

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In methanol
furaltadone
139-91-3

furaltadone

3-(5-acetylamino-furan-2-ylmethyleneamino)-5-morpholin-4-ylmethyl-oxazolidin-2-one
92654-06-3

3-(5-acetylamino-furan-2-ylmethyleneamino)-5-morpholin-4-ylmethyl-oxazolidin-2-one

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: H2 / Pd-C / methanol
2: 0.25 h
View Scheme
furaltadone
139-91-3

furaltadone

3-amino-5-(morpholinomethyl)oxazolidin-2-one
43056-63-9

3-amino-5-(morpholinomethyl)oxazolidin-2-one

Conditions
ConditionsYield
With spring onion leaf/root bulb at 25℃; for 12h;

139-91-3Related news

Development of An Enzyme-Linked Immunosorbent Assay for Determination of the Furaltadone (cas 139-91-3) Etabolite, 3-Amino-5-Morpholinomethyl-2-Oxazolidinone (AMOZ) in Animal Tissues09/30/2019

To determine 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ) residues released from protein bound AMOZ in animal tissues. Polyclonal and monoclonal antibodies were produced in this study. A rapid, sensitive, and specific competitive direct enzyme-linked immunosorbent assay (cdELISA) was dev...detailed

A novel chemiluminescent ELISA for detecting Furaltadone (cas 139-91-3) metabolite, 3-amino-5-morpholinomethyl-2-oxazolidone (AMOZ) in fish, egg, honey and shrimp samples10/01/2019

In this study, an indirect competitive enzyme-linked immunosorbent assay with chemiluminescent (CLELISA) detection for 3-amino-5-morpholinomethyl-2-oxazolidone (AMOZ) was developed. A monoclonal antibody (MAb) against AMOZ was prepared through immunizing BALB/c mice with 4-carboxybenzaldehyle de...detailed

139-91-3Relevant articles and documents

Process for formulating a synthetic drug for use in animal feed, and resulting formulation

-

, (2008/06/13)

A method of formulating a synthetic drug for use in animal feed, for the purpose of reducing carry-over of the synthetic drug to subsequent lots of animal feed in the feed mill.

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