Ampicillin Na - for cell culture , CAS No.69-52-3

CAS: 69-52-3 Cat. No.: A105484 Peso molecular: 371.39 Número EC: 200-708-1
Disponible para pedir
GRADE & PURITY for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements.
Synonyms
AMPICILLIN SODIUM (USP MONOGRAPH) | sodium (2S,5R,6R)-6-{[(2R)-2-amino-2-phenylacetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate | A836527 | Ampicillin (as sodium) | AMPICILLIN SODIUM [GREEN BOOK] | D-(-)-alpha-Aminobenzylpe
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
A105484-5g
3

39,90US$

46,90US$
Guardar 7,00 US$ (14.93%)
25g
A105484-25g
4

105,90US$

123,90US$
Guardar 18,00 US$ (14.53%)
100g
A105484-100g
4

285,90US$

333,90US$
Guardar 48,00 US$ (14.38%)
500g
A105484-500g
3

647,90US$

755,90US$
Guardar 108,00 US$ (14.29%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

for cell culture for Cell culture 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.

📋

Quality documents

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

📚

Literature proof

Cited in 63 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Ampicillin is reported as slightly soluble in water, practically insoluble in alcohol, chloroform, ether and fixed oils but soluble in dilute acids or bases. The solution should not be autoclaved; a stock solution should be sterilized through filtration and stored frozen, where it will be stable for months.
Used to select for ampicillin resistance in mutated and transformed cells.

Specifications

Sinónimos
AMPICILLIN SODIUM (USP MONOGRAPH) | sodium (2S, 5R, 6R)-6-{[(2R)-2-amino-2-phenylacetyl]amino}-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate | A836527 | Ampicillin (as sodium) | AMPICILLIN SODIUM [GREEN BOOK] | D-(-)-alpha-Aminobenzylpe
Especificaciones y pureza
for cell culture
Mecanismos bioquímicos y fisiológicos
Mode of Action: This is a β-lactam antibiotic that inhibits bacterial cell-wall synthesis by inactivating transpeptidases on the inner surface of the bacterial cell membrane. Mode of Resistance: Administration with β-lactamase cleaves the β-lactam ring
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
for Cell culture
Nombres e identificadores
Pubchem Sid504769486
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504769486
Sonrisas canónicasCC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)[O-])C.[Na+]
IUPAC Namesodium;(2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
InChIKeyKLOHDWPABZXLGI-YWUHCJSESA-M
INCHI1S/C16H19N3O4S.Na/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1
Isómeros SMILES CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)[C@@H](C3=CC=CC=C3)N)C(=O)[O-])C.[Na+]
Peso molecular 371.39
Reaxy-Rn 1231014
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1231014&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
ClaseCarboxylic 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 Penams  Aralkylamines  Benzene and substituted derivatives  Thiazolidines  Tertiary carboxylic acid amides  Amino acids  Azetidines  Thiohemiaminal derivatives  Propargyl-type 1,3-dipolar organic compounds  Azacyclic compounds  Monocarboxylic acids and derivatives  Carboximidic acids  Dialkylthioethers  Carboxylic acids  Hydrocarbon derivatives  Carbonyl compounds  Monoalkylamines  Organic oxides  Organic sodium salts  Organic zwitterions  Organopnictogen compounds  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents N-acyl-alpha amino acid or derivatives - Penam - Aralkylamine - Monocyclic benzene moiety - Benzenoid - Beta-lactam - Tertiary carboxylic acid amide - Thiazolidine - Azetidine - Carboxamide group - Amino acid - Lactam - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organic alkali metal salt - Organoheterocyclic compound - Thioether - Hemithioaminal - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Dialkylthioether - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Carbonyl group - Primary amine - Organic sodium salt - Amine - Organic oxide - Organic zwitterion - Organic salt - Organic nitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Aromatic heteropolycyclic compound
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
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GLA Tclin Alpha-galactosidase A (5444 Activities)
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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
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POLK Tbio DNA polymerase kappa (8653 Activities)
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POLI Tchem DNA polymerase iota (116820 Activities)
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POLH Tchem DNA polymerase eta (21678 Activities)
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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
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BLM Tchem Bloom syndrome protein (4248 Activities)
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GMNN Tbio Geminin (128009 Activities)
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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
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USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
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RUNX1 Tbio Runt-related transcription factor 1/Core-binding factor subunit beta (7867 Activities)
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GLS Tchem Glutaminase kidney isoform, mitochondrial (16997 Activities)
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Objetivos asociados (no humanos)
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rep Replicase polyprotein 1ab (378 Activities)
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fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
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CCT2 T-complex protein 1 subunit beta (5007 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

31 results found

Lot NumberCertificate TypeFechaArticulo
K2518289Certificate of AnalysisNov 08, 2025 A105484
K2518290Certificate of AnalysisNov 08, 2025 A105484
D2627082Certificate of AnalysisNov 08, 2025 A105484
K2518292Certificate of AnalysisNov 08, 2025 A105484
C2511047Certificate of AnalysisFeb 28, 2025 A105484
C2511046Certificate of AnalysisFeb 28, 2025 A105484
C2511054Certificate of AnalysisFeb 28, 2025 A105484
C2511052Certificate of AnalysisFeb 28, 2025 A105484
J2409138Certificate of AnalysisSep 28, 2024 A105484
J2409137Certificate of AnalysisSep 28, 2024 A105484
E2414213Certificate of AnalysisMay 09, 2024 A105484
E2414214Certificate of AnalysisMay 09, 2024 A105484
A2404037Certificate of AnalysisDec 15, 2023 A105484
A2404038Certificate of AnalysisDec 15, 2023 A105484
A2404189Certificate of AnalysisDec 15, 2023 A105484
A2404279Certificate of AnalysisDec 15, 2023 A105484
A2404028Certificate of AnalysisDec 15, 2023 A105484
A2404026Certificate of AnalysisDec 15, 2023 A105484
A2305013Certificate of AnalysisDec 17, 2022 A105484
A2305019Certificate of AnalysisDec 17, 2022 A105484
A2305018Certificate of AnalysisDec 17, 2022 A105484
A2305017Certificate of AnalysisDec 17, 2022 A105484
A2305016Certificate of AnalysisDec 17, 2022 A105484
A2305015Certificate of AnalysisDec 17, 2022 A105484
A2305014Certificate of AnalysisDec 17, 2022 A105484
L2214678Certificate of AnalysisMar 03, 2022 A105484
K2229864Certificate of AnalysisMar 03, 2022 A105484
C2224167Certificate of AnalysisMar 03, 2022 A105484
C2224124Certificate of AnalysisMar 03, 2022 A105484
C2224121Certificate of AnalysisMar 03, 2022 A105484
C2224120Certificate of AnalysisMar 03, 2022 A105484

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Propiedades químicas y físicas
SolubilidadH2O: soluble50 mg/mL
Punto de fusión (°C)215°C
Peso molecular371.400 g/mol
XLogP3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count6
Rotatable Bond Count4
Exact Mass371.092 Da
Monoisotopic Mass371.092 Da
Topological Polar Surface Area141.000 Ų
Heavy Atom Count25
Formal Charge0
Complexity568.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Preguntas frecuentes y artículos
Citations of This Product
Referencias
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4. Fujian Qin, Jiankang Li, Tianxiao Mao, Shuo Feng, Jing Li, Maode Lai.  (2023)  2 Hydroxybutyric Acid-Producing Bacteria in Gut Microbiome and Fusobacterium nucleatum Regulates 2 Hydroxybutyric Acid Level In Vivo.  Metabolites,  13  (3): (451).  [PMID:36984891] [10.3390/metabo13030451]
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14. Lingsha Cheng, Haoqian Wu, Xiaoying Cai, Youying Zhang, Siqi Yu, Yuanlong Hou, Zhe Yin, Qingyuan Yan, Qiong Wang, Taipeng Sun, Guangji Wang, Yonggui Yuan, Xueli Zhang, Haiping Hao, Xiao Zheng.  (2024)  A Gpr35-tuned gut microbe-brain metabolic axis regulates depressive-like behavior.  Cell Host & Microbe,      [PMID:38198925] [10.1016/j.chom.2023.12.009]
15. Luo Juan, Yu Yao, Wang Ke, He Sizhe, Wang Longjie, Liang Fangfang, Chin Jason W., Tang Shan.  (2024)  Capturing acyl–enzyme intermediates with genetically encoded 2,3-diaminopropionic acid for hydrolase substrate identification.  Nature Protocols,      [PMID:38867073] [10.1038/s41596-024-01006-x]
16. Runtao Zhu,Jiao Zhang,Lin Wang,Yunfeng Zhang,Yang Zhao,Ying Han,Jing Sun,Xi Zhang,Ying Dou,Huaxiong Yao,Wei Yan,Xiaozhou Luo,Junbiao Dai,Zhuojun Dai.  (2024)  Engineering functional materials through bacteria-assisted living grafting.  Cell Systems,      [PMID:38460522] [10.1016/j.cels.2024.02.003]
17. Liao Yiqi, Wang Yanfang, Huang Weirui, Wang Junxiang, Guo Mu, Zhang Jiahui, Zheng Hanlu, Yan Yingxue, Lin Zhaolong, Qiu Nengfu, Yu Xiangbin, Yu Yue.  (2024)  L. acidophilus/L. johnsonii ratio affects slow transit constipation in rats.  Scientific Reports,  14  (1): (1-13).  [PMID:39256411] [10.1038/s41598-024-71945-8]
18. Wei Wei, Yali Liu, Yuanlong Hou, Shuqi Cao, Zhuo Chen, Youying Zhang, Xiaoying Cai, Qingyuan Yan, Ziguang Li, Yonggui Yuan, Guangji Wang, Xiao Zheng, Haiping Hao.  (2024)  Psychological stress-induced microbial metabolite indole-3-acetate disrupts intestinal cell lineage commitment.  Cell Metabolism,      [PMID:38266651] [10.1016/j.cmet.2023.12.026]
19. Wu Qiong, Zhu Fangsi, Yao Yu, Chen Luyun, Ding Yijie, Su Yong, Ge Chaoliang.  (2024)  Sini san regulates intestinal flora and short-chain fatty acids to ameliorate hepatocyte apoptosis and relieve CCl4-induced liver fibrosis in mice.  Frontiers in Pharmacology,      [PMID:39281277] [10.3389/fphar.2024.1408459]
20. Weigang Wang, Na Yang, Liangliang Wang, Yuanxiang Zhu, Xiao Chu, Weijie Xu, Yawei Li, Yihai Xu, Lina Gao, Beibei Zhang, Guoqiang Zhang, Qinmiao Sun, Weihong Wang, Qiang Wang, Wenxin Zhang, Dahua Chen.  (2024)  The TET-Sall4-BMP regulatory axis controls craniofacial cartilage development.  Cell Reports,      [PMID:38427557] [10.1016/j.celrep.2024.113873]
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