cefazolin sodium salt - ≥97%(HPLC) , CAS No.27164-46-1

CAS: 27164-46-1 Cat. No.: C133095 Molecular Weight: 476.48 EC Number: 248-278-4
AVAILABLE TO ORDER
GRADE & PURITY ≥97%(HPLC)
Synonyms
AS-12230 | Cefabiozim | HMS3260H10 | HMS500A16 | SMR000058708 | AC-13166 | Cefazil | sodium (6R,7R)-3-{[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl}-8-oxo-7-[2-(1H-1,2,3,4-tetrazol-1-yl)acetamido]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | At
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
C133095-1g
3
$14.90
5g
C133095-5g
5
$27.90
25g
C133095-25g
5
$74.90
100g
C133095-100g
2
$239.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥97%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Cefazolin sodium salt inhibits synthesis of bacterial cell wall.
An inhibitor of bacterial cell wall synthesis

Specifications

Synonyms
AS-12230 | Cefabiozim | HMS3260H10 | HMS500A16 | SMR000058708 | AC-13166 | Cefazil | sodium (6R, 7R)-3-{[(5-methyl-1, 3, 4-thiadiazol-2-yl)sulfanyl]methyl}-8-oxo-7-[2-(1H-1, 2, 3, 4-tetrazol-1-yl)acetamido]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate | At
Specifications & Purity
≥97%(HPLC)
Biochemical and Physiological Mechanisms
Used to study the effect of expression, binding and inhibition of penicillin-binding proteins, especially PBP2 and PBP4 on bacterial cell wall mucopeptide synthesis.
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥97%(HPLC)
Names and Identifiers
Pubchem Sid504769603
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504769603
Canonical SmilesCC1=NN=C(S1)SCC2=C(N3C(C(C3=O)NC(=O)CN4C=NN=N4)SC2)C(=O)[O-].[Na+]
IUPAC Namesodium;(6R,7R)-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-8-oxo-7-[[2-(tetrazol-1-yl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
InChIKeyFLKYBGKDCCEQQM-WYUVZMMLSA-M
INCHI1S/C14H14N8O4S3.Na/c1-6-17-18-14(29-6)28-4-7-3-27-12-9(11(24)22(12)10(7)13(25)26)16-8(23)2-21-5-15-19-20-21;/h5,9,12H,2-4H2,1H3,(H,16,23)(H,25,26);/q;+1/p-1/t9-,12-;/m1./s1
Isomeric SMILES CC1=NN=C(S1)SCC2=C(N3[C@@H]([C@@H](C3=O)NC(=O)CN4C=NN=N4)SC2)C(=O)[O-].[Na+]
RTECS XI0390000
Molecular Weight 476.48
Reaxy-Rn 3585038
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3585038&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentN-acyl-alpha amino acids and derivatives
Alternative Parents Cephems  Alkylarylthioethers  1,3-thiazines  Thiadiazoles  Tetrazoles  Tertiary carboxylic acid amides  Heteroaromatic compounds  Azetidines  Thiohemiaminal derivatives  Sulfenyl compounds  Azacyclic compounds  Propargyl-type 1,3-dipolar organic compounds  Carboximidic acids  Carboxylic acids  Dialkylthioethers  Monocarboxylic acids and derivatives  Carbonyl compounds  Organonitrogen compounds  Hydrocarbon derivatives  Organopnictogen compounds  Organic oxides  Organic sodium salts  Organic zwitterions  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents N-acyl-alpha amino acid or derivatives - Cephem - Aryl thioether - Alkylarylthioether - Meta-thiazine - Azole - Beta-lactam - Heteroaromatic compound - Tertiary carboxylic acid amide - Tetrazole - Thiadiazole - Azetidine - Carboxamide group - Lactam - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Azacycle - Organic alkali metal salt - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Dialkylthioether - Thioether - Hemithioaminal - Sulfenyl compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic sodium salt - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Organic salt - Hydrocarbon derivative - Organic oxygen compound - Organopnictogen compound - Organic zwitterion - Organic oxide - Carbonyl group - Aromatic heteropolycyclic compound
DescriptionThis 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 organic sodium salt
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
POLK Tbio DNA polymerase kappa (8653 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLH Tchem DNA polymerase eta (21678 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC2 Tchem Canalicular multispecific organic anion transporter 1 (1191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCB11 Tchem Bile salt export pump (2311 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC3 Tbio Canalicular multispecific organic anion transporter 2 (718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BLM Tchem Bloom syndrome protein (4248 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCC4 Tchem Multidrug resistance-associated protein 4 (785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TGR Thioredoxin glutathione reductase (28579 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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 NumberCertificate TypeDateItem
B2625150Certificate of AnalysisMar 07, 2026 C133095
G2207202Certificate of AnalysisJan 20, 2026 C133095
G2207203Certificate of AnalysisJan 20, 2026 C133095
G2207206Certificate of AnalysisJan 20, 2026 C133095
G2207211Certificate of AnalysisJan 20, 2026 C133095
I2504766Certificate of AnalysisApr 11, 2024 C133095
I2504844Certificate of AnalysisApr 11, 2024 C133095
I2107404Certificate of AnalysisJun 15, 2023 C133095
I2107332Certificate of AnalysisJun 15, 2023 C133095
I2107357Certificate of AnalysisJun 15, 2023 C133095
L2004289Certificate of AnalysisSep 21, 2022 C133095

Show more ⌵

Chemical and Physical Properties
SolubilitySoluble in water (50 mg/ml), methanol (slightly), 100% ethanol (slightly), DMF, pyridine, and dioxane, aq.. Insoluble in acetone, chloroform, benzene, and ether.
SensitivityLight sensitive; Heat sensitive
Refractive Index1.96
Specific Rotation[α]-20° C
Melt Point(°C)190°C
Molecular Weight476.500 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count12
Rotatable Bond Count7
Exact Mass476.012 Da
Monoisotopic Mass476.012 Da
Topological Polar Surface Area238.000 Ų
Heavy Atom Count30
Formal Charge0
Complexity746.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Citations of This Product
References
1. Zhimei Wang, Yuehuan Zhang, Qing Chen, Xin Xiao, Carl Redshaw.  (2022)  Preparation of pelargonic acid vesicles and sustained drug release.  Canadian Journal of Chemistry,  101  (2):   [PMID:] [10.1139/cjc-2022-0075]
2. Yan-Mei Liang, Hui Yang, Bo Zhou, Yang Chen, Min Yang, Ke-Su Wei, Xiu-Fang Yan, Chao Kang.  (2021)  Waste tobacco leaves derived carbon dots for tetracycline detection: Improving quantitative accuracy with the aid of chemometric model.  ANALYTICA CHIMICA ACTA,      [PMID:35033278] [10.1016/j.aca.2021.339269]
3. Ying Wang, Xiaoguo Ma, Yuqi Peng, Yiyang Liu, Hengyuan Zhang.  (2021)  Selective and fast removal and determination of β-lactam antibiotics in aqueous solution using multiple templates imprinted polymers based on magnetic hybrid carbon material.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:34492906] [10.1016/j.jhazmat.2021.126098]
4. Tian-Xing Zhang, Shiyu Peng, Shu-Xin Zhang, Yutong Xue, Linzhu Su, Fang-Yuan Chen, Jie Gao, Qingxiang Guo, Jianfeng Liu, Fan Huang, Dong-Sheng Guo.  (2025)  Macrocycle-engineered liposomes for combating bacterial biofilm infections.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.164500]
5. Siqi Hong, Baoxi Fan, Zheng Wu, Xiaoyue Cheng, He Gao, Yanmin Jia, Cheng Liu, Luohong Zhang.  (2026)  Efficient piezoelectric catalytic degradation of organic pollutants by BTO@PANI via ultrasonic enhancement and energy-saving aeration.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2026.139543]
Solution Calculators
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