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Sodium cefamandole

CAS No.
30034-03-8
Chemical Name:
Sodium cefamandole
Synonyms
sodium cefamandole;CEFAMANDOLE SODIUM;Cephamandole sodium;CEFAMANDOLE SODIUM SALT;Cefamandole Sodium (250 mg);Sodium cefamandole USP/EP/BP;monosodiumsalt,d-hyl-1h-tetrazol-5-yl)thio)methyl)-8-oxo;5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylicacid,7-mandelamido-3-(((1-met;Sodium 7-D-mandelamido-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylate;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-mandelamido-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, monosodium salt, D- (8CI)
CBNumber:
CB3744569
Molecular Formula:
C18H17N6NaO5S2
Molecular Weight:
484.48
MDL Number:
MFCD07793339
MOL File:
30034-03-8.mol
Last updated:2023-06-08 09:02:24

Sodium cefamandole Properties

Melting point >175°C (dec.)
storage temp. Store at RT.
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form Solid
color White to Pale Yellow
Stability Moisture Sensitive
CAS DataBase Reference 30034-03-8(CAS DataBase Reference)
FDA UNII IY6234ODVR

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS07
Signal word  Danger
Hazard statements  H335-H319-H315-H334-H317
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P261-P285-P304+P341-P342+P311-P501-P264-P280-P302+P352-P321-P332+P313-P362-P261-P272-P280-P302+P352-P333+P313-P321-P363-P501
Hazard Codes  Xn
Risk Statements  36/37/38-42/43
Safety Statements  26-36
WGK Germany  2
RTECS  XI0389000
Toxicity mouse,LD50,intravenous,4460mg/kg (4460mg/kg),Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 26, Pg. 115, 1984.
NFPA 704
0
2 0

Sodium cefamandole price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 18138 Cefamandole (sodium salt) ≥95% 30034-03-8 25mg $49 2024-03-01 Buy
Cayman Chemical 18138 Cefamandole (sodium salt) ≥95% 30034-03-8 50mg $92 2024-03-01 Buy
Cayman Chemical 18138 Cefamandole (sodium salt) ≥95% 30034-03-8 100mg $172 2024-03-01 Buy
Cayman Chemical 18138 Cefamandole (sodium salt) ≥95% 30034-03-8 500mg $475 2024-03-01 Buy
TRC C237500 CefamandoleSodiumSalt 30034-03-8 1g $605 2021-12-16 Buy
Product number Packaging Price Buy
18138 25mg $49 Buy
18138 50mg $92 Buy
18138 100mg $172 Buy
18138 500mg $475 Buy
C237500 1g $605 Buy

Sodium cefamandole Chemical Properties,Uses,Production

Description

Cefamandole is a cephalosporin antibiotic that is effective against E. coli (MIC values range from 0.25-2 mg/L depending on strain) as well as H. influenza, S. pneumoniae, and S. aureus. It has been used to study the expression and inhibition of penicillin-binding proteins on bacterial cell walls and to study antibiotic resistance.

Chemical Properties

White Solid

Uses

Antibacterial;Bacterial transpeptidase inhibitor

Uses

Broad-spectrum semi-synthetic cephalosporin antibiotic.

Definition

ChEBI: An organic sodium salt that is the sodium salt of cefamandole.

in vitro

the in-vitro effect of cefamandole was tested against 645 strains of bacteria isolated from clinical sources. against gram-positive organisms cefamandole showed great potency, being three- to four-fold more active than cephalexin or cefoxitin. none of the pseudomonas aeruginosa strains were susceptible to 100 μg of cefamandole per ml [1].

in vivo

the testicular toxicity of cefamandole was evaluated in neonatal rats. results showed that cefamandole caused delayed maturity of the germinal epithelium of neonatal rats. in rats given daily subcutaneous injections during this period, the most mature germinal cells were acrosome phase spermatids [2].

References

[1] eickhoff tc, ehret jm. in vitro comparison of cefoxitin, cefamandole, cephalexin, and cephalothin. antimicrob agents chemother. 1976 jun;9(6):994-9.
[2] hoover dm, buening mk, tamura rn, steinberger e. effects of cefamandole on spermatogenic development of young cd rats. fundam appl toxicol. 1989 nov;13(4):737-46.
[3] delgado dg, brau cj, cobbs cg, dismukes we. clinical and laboratory evaluation of cefamandole in the therapy of haemophilus spp. bronchopulmonary infections. antimicrob agents chemother. 1979 jun;15(6):807-12.

Sodium cefamandole Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 103)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49374 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29811 58
SIMAGCHEM CORP
+86-13806087780 sale@simagchem.com China 17365 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 7724 58
Baoji Guokang Healthchem co.,ltd
+8615604608665 15604608665 dominicguo@gk-bio.com CHINA 9414 58
Dayang Chem (Hangzhou) Co.,Ltd.
571-88938639 +8617705817739 info@dycnchem.com China 52849 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24727 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49978 58
Shenzhen Excellent Biomedical Technology Co.,Ltd.
+86-0755-26050679 +86-15915472436 sale@ex-biotech.cn China 1031 58

View Lastest Price from Sodium cefamandole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Sodium cefamandole pictures 2020-05-25 Sodium cefamandole
30034-03-8
US $0.00-0.00 / Kg 1KG 99.0%+ 300 MT Shaanxi Dideu Medichem Co. Ltd
Sodium cefamandole pictures 2020-01-19 Sodium cefamandole
30034-03-8
US $3.00 / KG 1KG 98% 1kg,5kg,50kg Career Henan Chemical Co
(6R,7R)-7-[[(2R)-2-Hydroxy-2-phenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Sodium Salt CEFAMANDOLE SODIUM CEFAMANDOLE SODIUM SALT 5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylicacid,7-mandelamido-3-(((1-met monosodiumsalt,d-hyl-1h-tetrazol-5-yl)thio)methyl)-8-oxo (6R,7R)-7-[(R)-2-Hydroxy-2-phenylacetylamino]-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid sodium salt Cephamandole sodium Cefamandole Sodium (250 mg) sodium [6r-[6alpha,7beta(r*)]]-7-[[(formyloxy)phenylacetyl]amino]-3-[[(1-methyl-1h-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate sodium (6r-(6alpha,7beta(r*)))-7-((hydroxyphenylacetyl)amino)-3-(((1-methyl-1h-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylate sodium cefamandole 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[(hydroxyphenylacetyl)amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, monosodium salt, [6R-[6α,7β(R*)]]- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2R)-hydroxyphenylacetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, monosodium salt, (6R,7R)- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-mandelamido-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, monosodium salt, D- (8CI) Sodium 7-D-mandelamido-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylate Sodium cefamandole USP/EP/BP 30034-03-8 C18H17N6O5S2Na C18H17N6NaO5S2 48448 BioChemical Antibiotics Antibiotics A to Z Antibiotics A-F A - KAntibiotics Antibacterial Antibiotics A to Antibiotics A-FAntibiotics Chemical Structure Class Interferes with Cell Wall SynthesisAntibiotics Mechanism of Action Penicillins and Cephalosporins (beta-Lactams) Spectrum of Activity Nucleotides and Nucleosides Bases & Related Reagents Intermediates & Fine Chemicals Nucleotides Pharmaceuticals Sulfur & Selenium Compounds