Tylosin solution - BioReagent, for cell culture, 0.1 μm filtered, 8 mg/mL in 0.9% NaCl , CAS No.74610-55-2

CAS: 74610-55-2 Cat. No.: T433510 Summenformel: 2(C46H77NO17).C4H6O6 EG-Nummer: 616-119-1
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GRADE & PURITY BioReagent ? BioReagent grade — tested suitable for life-science and molecular-biology use. Use for cell culture, assays, and biochemical work needing biological compatibility. for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. 0.1 μm filtered, 8 mg/mL in 0.9% NaCl
Synonyms
s3162 | TYLOSIN TARTRATE [USP MONOGRAPH] | Tylosin, (2R,3R)-2,3-dihydroxybutanedioate (1:1) | Tylosin tartrate (USP) | Tylosin (tartrate) | NSC 758961 | Tylan injectable | EINECS 215-781-5 | DTXSID3045938 | Tylosin tartrate, potency: >=800 units/mg tylosi
Storage
Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
Size
Deutschland (EU)
USA*
Price
Qty
20ml
T433510-20ml
1 Auf Lager
16,40€
Enter a quantity for the sizes you want to add.
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Why this grade

BioReagent, for cell culture, 0.1 μm filtered, 8 mg/mL in 0.9% NaCl BioReagent,für die Zellkultur for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C,Desiccated Ships Ice chest + Ice pads 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.

📚

Literature proof

Cited in 14 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

General Description

Chemical structure: macrolide Tylosin is a macrolide antibiotic, which comprises of a 16-member lactone ring. This solution is recommended for use at 1 mL/L.


Application

Tylosin solution has been used as an antimicrobial agent in antibiotic susceptibility minimal inhibitory concentration(MIC) of E. coli and S. aureus isolates. It has also been used as a component of Dulbecco′s modified Eagle′s (DMEM) medium for self-inactivating lentivirus production and skin fibroblast cultivation.


Other Notes

Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage.

Specifications

Synonyme
s3162 | TYLOSIN TARTRATE [USP MONOGRAPH] | Tylosin, (2R,3R)-2,3-dihydroxybutanedioate (1:1) | Tylosin tartrate (USP) | Tylosin (tartrate) | NSC 758961 | Tylan injectable | EINECS 215-781-5 | DTXSID3045938 | Tylosin tartrate, potency: >=800 units/mg tylosi
Spezifikationen & Reinheit
BioReagent, for cell culture, 0.1 μm filtered, 8 mg/mL in 0.9% NaCl
Biochemische und physiologische Mechanismen
Tylosin inhibits bacterial protein synthesis by binding to the large subunit 50S. It is effective against Gram-positive bacteria and mycoplasma and is used in veterinary medicine. It has been used to study implant site abscess prevention in cattle and M
Storage
Store at -20°C,Desiccated
Verschickt in
Ice chest + Ice pads
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Note
BioReagent, für die Zellkultur
Aktionsart
INHIBITOR
Namen und Kennungen
Pubchem Sid528772914
Kanonisches LächelnO[C@H]([C@@H](O)C(O)=O)C(O)=O.CC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@@H](O[C@H]3C[C@@](C)(O)[C@@H](O)[C@H](C)O3)[C@@H]([C@H]2O)N(C)C)[C@@H](CC=O)C[C@@H](C)C(=O)\C=C\C(C)=C\[C@@H]1CO[C@@H]4O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]4OC
IUPAC Name(2R,3R)-2,3-dihydroxybutanedioic acid;2-[(4R,5S,6S,7R,9R,11E,13E,15R,16R)-6-[(2R,3R,4R,5S,6R)-5-[(2S,4R,5S,6S)-4,5-dihydroxy-4,6-dimethyloxan-2-yl]oxy-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-16-ethyl-4-hydroxy-15-[[(2R,3R,4R,5R,6R)-5-hydroxy-3,4-dimethoxy-6-methyloxan-2-yl]oxymethyl]-5,9,13-trimethyl-2,10-dioxo-1-oxacyclohexadeca-11,13-dien-7-yl]acetaldehyde
InChIKeyICVKYYINQHWDLM-KBEWXLTPSA-N
INCHI1S/C46H77NO17.C4H6O6/c1-13-33-30(22-58-45-42(57-12)41(56-11)37(52)26(5)60-45)18-23(2)14-15-31(49)24(3)19-29(16-17-48)39(25(4)32(50)20-34(51)62-33)64-44-38(53)36(47(9)10)40(27(6)61-44)63-35-21-46(8,55)43(54)28(7)59-35;5-1(3(7)8)2(6)4(9)10/h14-15,17-18,24-30,32-33,35-45,50,52-55H,13,16,19-22H2,1-12H3;1-2,5-6H,(H,7,8)(H,9,10)/b15-14+,23-18+;/t24-,25+,26-,27-,28+,29+,30-,32-,33-,35+,36-,37-,38-,39-,40-,41-,42-,43+,44+,45-,46-;1-,2-/m11/s1
Isomere SMILES CC[C@@H]1[C@H](/C=C(/C=C/C(=O)[C@@H](C[C@@H]([C@@H]([C@H]([C@@H](CC(=O)O1)O)C)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)C)O[C@H]3C[C@@]([C@H]([C@@H](O3)C)O)(C)O)N(C)C)O)CC=O)C)\C)CO[C@H]4[C@@H]([C@@H]([C@@H]([C@H](O4)C)O)OC)OC.[C@@H]([C@H](C(=O)O)O)(C(=O)O)O

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 oxygen compounds
KlasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides
Direct ParentAminoglycosides
Alternative Parents Macrolides and analogues  Disaccharides  O-glycosyl compounds  Short-chain hydroxy acids and derivatives  Beta hydroxy acids and derivatives  Sugar acids and derivatives  Oxanes  Alpha hydroxy acids and derivatives  Fatty acids and conjugates  Dicarboxylic acids and derivatives  Alpha-hydrogen aldehydes  Tertiary alcohols  Secondary alcohols  1,2-aminoalcohols  Cyclic ketones  Trialkylamines  Lactones  Amino acids and derivatives  Carboxylic acid esters  Oxacyclic compounds  Acetals  Dialkyl ethers  Carboxylic acids  Hydrocarbon derivatives  Organopnictogen compounds  Organic oxides  
Molecular FrameworkNot available
Substituents Aminoglycoside core - Macrolide - Disaccharide - Glycosyl compound - O-glycosyl compound - Beta-hydroxy acid - Short-chain hydroxy acid - Sugar acid - Alpha-hydroxy acid - Dicarboxylic acid or derivatives - Hydroxy acid - Fatty acid - Oxane - Tertiary alcohol - Alpha-hydrogen aldehyde - Secondary alcohol - Tertiary aliphatic amine - Tertiary amine - Cyclic ketone - Lactone - Ketone - 1,2-aminoalcohol - Amino acid or derivatives - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Ether - Carboxylic acid derivative - Carboxylic acid - Dialkyl ether - Acetal - Organic nitrogen compound - Aldehyde - Amine - Organopnictogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Aliphatic heteromonocyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars.
External Descriptors Not available
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

3 results found

Lot NumberCertificate TypeDatumArtikel
H2323128Certificate of AnalysisJun 09, 2026 T433510
E2628585Certificate of AnalysisApr 30, 2026 T433510
C2503442Certificate of AnalysisFeb 14, 2025 T433510
Chemische und physikalische Eigenschaften
Molekulargewicht1066.200 g/mol
XLogP3
Hydrogen Bond Donor Count9
Hydrogen Bond Acceptor Count24
Rotatable Bond Count16
Exact Mass1065.54 Da
Monoisotopic Mass1065.54 Da
Topological Polar Surface Area354.000 Ų
Heavy Atom Count74
Formal Charge0
Complexity1700.000
Isotope Atom Count0
Defined Atom Stereocenter Count23
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count2
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds2
Covalently-Bonded Unit Count2
FAQs und Artikel
Citations of This Product
Referenzen
1. Bing Wang, Qingtong Cao, Ming Cheng, Guomin Li, Jian Zhang, Hong Jiang.  (2023)  Photocatalytic degradation of antibiotics in water by pollution-free photocatalytic films with a three-dimensional layered structure and the reaction mechanism study.  Journal of Water Process Engineering,      [PMID:] [10.1016/j.jwpe.2023.103550]
2. Zhiyan Huang, Tenglu Wang, Minxian Shen, Zhujian Huang, Yunxiao Chong, Lihua Cui.  (2019)  Coagulation treatment of swine wastewater by the method of in-situ forming layered double hydroxides and sludge recycling for preparation of biochar composite catalyst.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2019.03.136]
3. Chan-Yuan YAO, Jin-Yi YANG, Zhen-Lin XU, Hong WANG, Hong-Tao LEI, Yuan-Ming SUN, Yuan-Xin TIAN, Yu-Dong SHEN.  (2018)  Indirect Competitive Enzyme-Linked Immunosorbent Assay for Detection of Tylosin in Milk and Water Samples.  CHINESE JOURNAL OF ANALYTICAL CHEMISTRY,      [PMID:] [10.1016/S1872-2040(18)61106-5]
4. Yuehong Song, Shanshan Song, Liqiang Liu, Hua Kuang, Lingling Guo, Chuanlai Xu.  (2015)  Simultaneous detection of tylosin and tilmicosin in honey using a novel immunoassay and immunochromatographic strip based on an innovative hapten.  FOOD AND AGRICULTURAL IMMUNOLOGY,      [PMID:] [10.1080/09540105.2015.1089843]
5. Liubing Fan, Shiqiang Hao, Shihui He, Xusheng Zhang, Mingyang Li, Christopher Wolverton, Jing Zhao, Quanlin Liu.  (2023)  Luminescent hybrid halides with various centering metal cations (Zn, Cd and Pb) and diverse structures.  DALTON TRANSACTIONS,  52  (16): (5119-5126).  [PMID:36961101] [10.1039/D2DT04067K]
6. Tian-Yu Qiu, Ying-Nan Zhao, Wen-Si Tang, Hua-Qiao Tan, Hui-Ying Sun, Zhen-Hui Kang, Xia Zhao, Yang-Guang Li.  (2022)  Smart Covalent Organic Framework with Proton-Initiated Switchable Photocatalytic Aerobic Oxidation.  ACS Catalysis,      [PMID:] [10.1021/acscatal.2c03796]
7. Wang-Xi Fan, Zefang Li, Zhou Yang, Jun-Fei Ou, Meng Xiang, Zhong-Li Qin.  (2022)  Improving the curing and flame retardancy of epoxy resin composites by multifunctional Si-containing cyclophosphazene derivatives.  RSC Advances,  12  (22): (13756-13764).  [PMID:35530380] [10.1039/D1RA08843B]
8. Xin Chen, Duanxiu Li, Yanwen Duan, Yong Huang.  (2022)  Characterization of co-amorphous sinomenine-tranilast systems with strong intermolecular interactions and sustained release profiles.  JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.jddst.2022.103296]
9. Haiyun Li, Yizhi Qiu, Tuo Yao, Yachun Ma, Huirong Zhang, Xiaolei Yang, Changning Li.  (2019)  Evaluation of seven chemical pesticides by mixed microbial culture (PCS-1): Degradation ability, microbial community, and Medicago sativa phytotoxicity.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:31843407] [10.1016/j.jhazmat.2019.121834]
10. Xiangqian Li, Jiapei Gu, Zhan Zhou, Wanqiang Liu, Jinwei Gao, Qianming Wang.  (2019)  Precise control for the aggregation and deaggregation with the aid of a tetraphenylethylene derivative: Luminescence modulation and sensing performance.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2019.107844]
11. Tianlu Xu, Chunling Zhang, Peihong Li, Xueyan Dai, Lijie Qu, Yanlong Sui, Jinjia Gu, Yanli Dou.  (2018)  Preparation of dual-functionalized graphene oxide for the improvement of the thermal stability and flame-retardant properties of polysiloxane foam.  NEW JOURNAL OF CHEMISTRY,  42  (16): (13873-13883).  [PMID:] [10.1039/C8NJ02361A]
12. Dong Zhou, Ruliang Liu, Yan-Bing He, Fengyun Li, Ming Liu, Baohua Li, Quan-Hong Yang, Qiang Cai, Feiyu Kang.  (2016)  SiO2 Hollow Nanosphere-Based Composite Solid Electrolyte for Lithium Metal Batteries to Suppress Lithium Dendrite Growth and Enhance Cycle Life.  Advanced Energy Materials,  (7): (1502214).  [PMID:] [10.1002/aenm.201502214]
13. Yuzhen Xu, Liyan Qiu.  (2015)  Nonspecifically enhanced therapeutic effects of vincristine on multidrug-resistant cancers when coencapsulated with quinine in liposomes.  International Journal of Nanomedicine,      [PMID:26170660] [10.2147/IJN.S84555]
14. Yvhao Xie, Xinxin Li, Qingshi Meng, Jinjun Li, Xin Wang, Liying Zhu, Weiwei Wang, Xiaoqiong Li.  (2024)  Interplay between gut microbiota and tryptophan metabolism in type 2 diabetic mice treated with metformin.  Microbiology Spectrum,      [PMID:39162538] [10.1128/spectrum.00291-24]
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