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23696-28-8

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  • High Quality 99% 2-Quinoxalinecarboxamide,N-(2-hydroxyethyl)-3-methyl-, 1,4-dioxide 23696-28-8 ISO Producer

    Cas No: 23696-28-8

  • USD $ 0.1-0.1 / Gram

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  • Xi'an Xszo Chem Co., Ltd.
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23696-28-8 Usage

Description

Different sources of media describe the Description of 23696-28-8 differently. You can refer to the following data:
1. Olaquindox is an antibacterial derivative of quinoxaline, used as a growth promoter for pigs.
2. Olaquindox is an antibiotic and a swine growth regulator. In vivo, olaquindox (100 mg/kg) decreases E. coli-induced diarrhea and the number of intraepithelial lymphocytes in the ileum and increases body weight in geld piglets. Olaquindox induces bleeding, intramuscular edema, vacuolar degeneration, and deformation of renal tubules in C. carpio. It decreases mean body weight and increases the number of dead fetuses in pregnant rats when administered at a dose of 110 mg/kg and increases the number of external deformities, including bent tail, craniorachischisis, exencephaly, and anophthalmia in rat pups born to exposed pregnant mothers. Formulations containing olaquindox have been used as growth promoting agents in bovine livestock.

Chemical Properties

Pale Yellow Crystalline Solid

Uses

Different sources of media describe the Uses of 23696-28-8 differently. You can refer to the following data:
1. It can be found in Bayo-N-Ox and Proquindox and numerous oilier pig feed. It is a photosensitizer and forms a reactive oxyziridine on exposure to light. It can also induce photo allergie contact dermatitis and persistent light reactions in pig breeders.
2. Olaquindox is a growth promotor in pig-breeding; acts as a chemotherapeutic agent prophylactically used to lower the frequency of bacterial enteritis in pigs.

Contact allergens

Olaquindox is an antibacterial agent derivative of quinoxaline, used as a growth promoter of pigs. It can be found in Bayo-N-Ox? and Proquindox? and numerous other pig feeds. It is a photosensitizer that forms reactive photoproducts on light exposure. It can induce photoallergic contact dermatitis and persistent light reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 23696-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,6,9 and 6 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23696-28:
(7*2)+(6*3)+(5*6)+(4*9)+(3*6)+(2*2)+(1*8)=128
128 % 10 = 8
So 23696-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N3O4/c1-8-11(12(17)13-6-7-16)15(19)10-5-3-2-4-9(10)14(8)18/h2-5,16H,6-7H2,1H3,(H,13,17)

23696-28-8 Well-known Company Product Price

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  • Sigma-Aldrich

  • (33987)  Olaquindox  VETRANAL, analytical standard

  • 23696-28-8

  • 33987-100MG-R

  • 945.36CNY

  • Detail

23696-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-hydroxyethyl)-3-methyl-4-oxido-1-oxoquinoxalin-1-ium-2-carboxamide

1.2 Other means of identification

Product number -
Other names Bayernox

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Veterinary Drug: GROWTH_PROMOTER
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:23696-28-8 SDS

23696-28-8Relevant articles and documents

An Improved and Efficient Synthesis of Quinoxalinecarboxamide 1,4-Dioxides from Benzofuroxan and Acetoacetamides in the Presence of Calcium Salts

Stumm, G.,Niclas, H.-J.

, p. 736 - 744 (2007/10/02)

An improved and efficient method for the preparation of the title compounds 3 is described.Thus, quinoxalinecarboxamide 1,4-dioxides 3 are synthesized in high yields by reaction of benzofuroxan 1 with acetoacetamides 2 in the presence of catalytic amounts of calcium salts and ethanolamine.The reaction is assumed to involve a chelate mechanism with 4 as intermediate.Side reactions are studied by means of HPLC and TLC.

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