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Ceftiofur HCl - ≥95%, high purity , CAS No.103980-44-5

COA

Grade & Purity:

≥95%

Cas Number: 103980-44-5
Molecular Weight: 560.02
MDL number: MFCD04038020
PubChem CID: 9937686
PubChem SID: 488196449

In stock

Item Number

C129274

Grouped product items
SKU	Size	Availability	Price
C129274-250mg	250mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$34.90
C129274-1g	1g	3	$103.90
C129274-5g	5g	4	$343.90
C129274-10g	10g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$617.90
C129274-25g	25g	4	$1,373.90
C129274-100g	100g	2	$3,433.90

Broad spectrum antibiotic agent. Irreversible PBP transpeptidase inhibitor.

View related series

Anti-infection (2803) Antibiotic (1629) Bacterial (3013)

Basic Description

Synonyms	5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(((2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl)amino)-3-(((2-furanylcarbonyl)thio)methyl)-8-oxo, monohydrochloride, (6R,7R) \| Ceftiofur, HCl \| Spectramast LC Sterile Suspension \| DTXSID101034300 \|
Specifications & Purity	≥95%
Biochemical and Physiological Mechanisms	Ceftiofur Hydrochloride is a cephalosporin antibiotic. The compound is a derivative of a third generation cephalosporin, Ceftiofur. Ceftiofur has been used in bovine studies and in antibiotic resistancy studies of Escherichia coli and Salmonella enterica.
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Ceftiofur HCl is a hydrochloride of ceftiofur that is a broad spectrum cephalosporin. A cephalosporin antibiotic resistant to beta-lactamase.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 N-acyl-alpha amino acids and derivatives

Kingdom	Organic compounds
Superclass	Organic acids and derivatives
Class	Carboxylic acids and derivatives
Subclass	Amino acids, peptides, and analogues
Intermediate Tree Nodes	Amino acids and derivatives - Alpha amino acids and derivatives
Direct Parent	N-acyl-alpha amino acids and derivatives
Alternative Parents	Cephems Furoic acid and derivatives 1,3-thiazines Thiazoles Tertiary carboxylic acid amides Heteroaromatic compounds Thioesters Azetidines Carbothioic S-esters Isothioureas Thiohemiaminal derivatives Azacyclic compounds Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Carboximidic acids Monocarboxylic acids and derivatives Dialkylthioethers Oxacyclic compounds Carboxylic acids Organonitrogen compounds Organic oxides Hydrocarbon derivatives Hydrochlorides Carbonyl compounds
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	N-acyl-alpha amino acid or derivatives - Cephem - Furoic acid or derivatives - Meta-thiazine - Azole - Beta-lactam - Furan - Tertiary carboxylic acid amide - Thiazole - Heteroaromatic compound - Carbothioic s-ester - Carboxamide group - Azetidine - Isothiourea - Lactam - Thiocarboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Carboximidic acid - Carboximidic acid derivative - Dialkylthioether - Carboxylic acid - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Thioether - Hemithioaminal - Thiocarboxylic acid or derivatives - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Hydrochloride - Hydrocarbon derivative - Carbonyl group - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488196449
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488196449
IUPAC Name	(6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(furan-2-carbonylsulfanylmethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;hydrochloride
INCHI	InChI=1S/C19H17N5O7S3.ClH/c1-30-23-11(9-7-34-19(20)21-9)14(25)22-12-15(26)24-13(17(27)28)8(5-32-16(12)24)6-33-18(29)10-3-2-4-31-10;/h2-4,7,12,16H,5-6H2,1H3,(H2,20,21)(H,22,25)(H,27,28);1H/b23-11-;/t12-,16-;/m1./s1
InChIKey	KEQFDTJEEQKVLM-JUODUXDSSA-N
Smiles	CON=C(C1=CSC(=N1)N)C(=O)NC2C3N(C2=O)C(=C(CS3)CSC(=O)C4=CC=CO4)C(=O)O.Cl
Isomeric SMILES	CO/N=C(/C1=CSC(=N1)N)\C(=O)N[C@H]2[C@@H]3N(C2=O)C(=C(CS3)CSC(=O)C4=CC=CO4)C(=O)O.Cl
Molecular Weight	560.02
Reaxy-Rn	38065090
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=38065090&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot Number	Certificate Type	Date	Item
K1906063	Certificate of Analysis	Mar 04, 2025	C129274
E2309824	Certificate of Analysis	Feb 07, 2025	C129274
E2309896	Certificate of Analysis	Feb 07, 2025	C129274
E2309835	Certificate of Analysis	Feb 07, 2025	C129274
E2309819	Certificate of Analysis	Feb 07, 2025	C129274
E2309901	Certificate of Analysis	Feb 07, 2025	C129274
E2309903	Certificate of Analysis	Feb 07, 2025	C129274
E2309829	Certificate of Analysis	Feb 07, 2025	C129274
E2309893	Certificate of Analysis	Feb 07, 2025	C129274
E1528114	Certificate of Analysis	Dec 08, 2022	C129274
H2215243	Certificate of Analysis	Aug 18, 2022	C129274

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Chemical and Physical Properties

Solubility	Soluble in methanol, water (<1 mg/ml at 25 °C), DMSO (112 mg/ml at 25 °C), and ethanol (40 mg/ml at 25 °C).
Molecular Weight	560.000 g/mol
XLogP3
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	13
Rotatable Bond Count	9
Exact Mass	559.006 Da
Monoisotopic Mass	559.006 Da
Topological Polar Surface Area	256.000 Å²
Heavy Atom Count	35
Formal Charge	0
Complexity	945.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	2
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	1
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	1
Covalently-Bonded Unit Count	2

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