Ceforanide

Product Name: Ceforanide
CAS No.: 60925-61-3
Chemical Name: Ceforanide
Synonyms: C06884;BL-S-786;Ceforanide;CEFORANIDE (200 MG);Antibiotic BL-S-786;Ceforanide USP/EP/BP;Ceforanide (1097807);2-(2,4-Dimethylphenyl)sulf;Bacterial,inhibit,Antibiotic,Inhibitor,Ceforanide;(6R,7R)-7-(2-(2-(Aminomethyl)phenyl)acetamido)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CBNumber: CB2501637
Molecular Formula: C20H21N7O6S2
Formula Weight: 519.55
MOL File: 60925-61-3.mol

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Ceforanide Property

Melting point:: >150° (dec)
Density: 1.79±0.1 g/cm3(Predicted)
storage temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility: Aqueous Base (Slightly), DMSO (Slightly, Heated), Methanol (Slightly)
pka: 2.52±0.10(Predicted)
form: Solid
color: White to Pale Brown
Stability:: Hygroscopic
InChIKey: SLAYUXIURFNXPG-CRAIPNDOSA-N

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Safety

HS Code: 2941906000

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H317May cause an allergic skin reaction

H334May cause allergy or asthma symptoms or breathing difficulties if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P284Wear respiratory protection.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P342+P311IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 1097807
Product name: Ceforanide
Packaging: 200mg
Price: $377
Updated: 2024/03/01

TRC

Product number: C242930
Product name: Ceforanide
Packaging: 50mg
Price: $275
Updated: 2021/12/16

TRC

Product number: C242930
Product name: Ceforanide
Packaging: 100mg
Price: $495
Updated: 2021/12/16

Medical Isotopes, Inc.

Product number: 63540
Product name: Ceforanide
Packaging: 100mg
Price: $1025
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FA41015
Product name: (6R,7R)-7-[[2-[2-Aminomethyl)phenyl]acetyl]amino]-3-[[1-(carboxymethyl)tetrazol-5-yl]sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Packaging: 1g
Price: $290
Updated: 2021/12/16

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Ceforanide Chemical Properties,Usage,Production

Description

Ceforanide is a second generation cephalosporin with good β-lactamase resistance. It has a serum half-life of about three hours, allowing twice-daily dosing.

Originator

Bristol (USA)

Uses

Ceforanide is a cephalosporin based antibiotic used in the sterilization in various medical procedures.

Uses

Cephalosporin antibiotic

Definition

ChEBI: A second-generation cephalosporin antibiotic with {[1-(carboxymethyl)-1H-tetrazol-5-yl]sulfanyl}methyl and 2-(aminomethyl)phenylacetamido groups at positions 3 and 7, respectively, of the cephem skeleton. It is effective against many col forms, including Escherichia coli, Klebsiella, Enterobacter and Proteus, and most strains of Salmonella, Shigella, Hemophilus, Citrobacter and Ari ona species.

brand name

Precef (Apothecon).

Antimicrobial activity

A semisynthetic parenteral cephalosporin with activity broadly similar to that of cefalotin. Its activity in vitro is significantly reduced in the presence of serum. A 1 g intravenous dose achieves a concentration of c. 135 mg/L at the end of infusion. The response after 0.25, 0.5 and 1 g intravenous doses is essentially linear. A 1 g intramuscular dose produces mean peak values of around 70 mg/L. Plasma protein binding is around 85%.
It is almost entirely eliminated in the urine with a halflife of about 2.5 h, 80–95% being recovered in the first 12 h. The half-life is inversely related to renal function, rising to around 20 h when the creatinine clearance falls below 5 mL/min. About half the dose is removed by hemodialysis over 6 h.
It is generally well tolerated; phlebitis and pain at the site of injection are reported in some patients with occasional transient neutropenia and increased transaminase levels. It has been used principally for the treatment of infections due to Gram-positive cocci, including staphylococcal and streptococcal soft-tissue infections, but is no longer widely available.

Ceforanide Preparation Products And Raw materials

Raw materials

Preparation Products

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Ceforanide Suppliers

China 65 Germany 1 India 4 United Kingdom 3 United States 13 Global 86

BOC Sciences

Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Country: United States
ProdList: 14055
Advantage: 65

TargetMol Chemicals Inc.

Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Country: United States
ProdList: 32165
Advantage: 58

Aladdin Scientific

Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Country: United States
ProdList: 57505
Advantage: 58

TargetMol Chemicals Inc.

Tel
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Country: United States
ProdList: 38632
Advantage: 58

United States Biological

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Country: United States
ProdList: 6075
Advantage: 58

United States Biological

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Email: chemicals@usbio.net
Country: United States
ProdList: 6214
Advantage: 80

MedChemExpress

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Country: United States
ProdList: 6398
Advantage: 58

Riedel-de Haen AG

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Country: United States
ProdList: 6773
Advantage: 87

Alfa Chemistry

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Country: United States
ProdList: 6814
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CarboMer, Inc.

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Email: sales@carbomer.com
Country: United States
ProdList: 4026
Advantage: 67

AvaChem Scientific LLC

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Email: Info@avachem.com
Country: United States
ProdList: 315
Advantage: 30

Waterstone Technology, LLC

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Email: sales@waterstonetech.com
Country: United States
ProdList: 6786
Advantage: 30

AK Scientific, Inc.

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Email: sales@aksci.com
Country: United States
ProdList: 6347
Advantage: 65

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View Lastest Price from Ceforanide manufacturers

Shaanxi Dideu Medichem Co. Ltd

Product: Ceforanide 60925-61-3
Price: US $0.00-0.00/Kg
Min. Order: 1KG
Purity: 99.0%
Supply Ability: 500 MT
Release date: 2020-05-25

Career Henan Chemical Co

Product: Ceforanide 60925-61-3
Price: US $7.00/kg
Min. Order: 1kg
Purity: 99%
Supply Ability: 100kg
Release date: 2018-12-21

60925-61-3, CeforanideRelated Search:

Acetyl chloride PHENYL VALERATE Acetaminophen Acetylacetone Acetyl coenzyme A sodium salt 2-aminomethylphenylacetic acid (intermediate of ceforanide) 2-(5-Mercaptotetrazole-1-yl)ethanol 1H-Tetrazole-1-acetic acid 7-TMCA 7-Phenyl-acetamido-deacetoxy-cephalosporanic-acid 1-Ethyl-1H-1,2,3,4-tetrazole-5-thiol Phenylacetic acid 5-Mercapto-1H-tetrazole-1-acetic acid 1-ETHYL-1H-TETRAZOLE Ceforanide Acetyl-resveratrol ACETAMINOPHENOL BP/USP 1H-Tetrazole, 5-((3-(ethylthio)propyl)thio)-1-methyl-

CEFORANIDE (200 MG)

Ceforanide

(6R,7R)-7α-[[(2-Aminomethylphenyl)acetyl]amino]-3-[[[1-(carboxymethyl)-1H-tetrazol-5-yl]thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Antibiotic BL-S-786

BL-S-786

C06884

5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[2-[2-(aMinoMethyl)phenyl]acetyl]aMino]-3-[[[1-(carboxyMethyl)-1H-tetrazol-5-yl]thio]Methyl]-8-oxo-,(6R,7R)-

(6R,7R)-7-[[2-[2-(Aminomethyl)phenyl]acetyl]amino]-3-[[1-(carboxymethyl)tetrazol-5-yl]sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

2-(2,4-Dimethylphenyl)sulf

Ceforanide USP/EP/BP

(6R,7R)-7-(2-(2-(Aminomethyl)phenyl)acetamido)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

Ceforanide (1097807)

Bacterial,inhibit,Antibiotic,Inhibitor,Ceforanide

60925-61-3

C20H21N7O6S2

Ceforanide