Tylosin - 10mM in DMSO , CAS No.1401-69-0

CAS: 1401-69-0 Cat. No.: T421501 Peso molecular: 916.12 Número EC: 215-754-8 PubChem CID: 5280440
Disponible para pedir
GRADE & PURITY 10mM in DMSO
Synonyms
Antibiotic obtained from cultures of Streptomyces fradiae, or the same substance produced by any other means | TYLOSIN [MI] | SR-05000002057-3 | TYLOSIN (USP-RS) | 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-
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
T421501-1ml
1

164,90US$

241,90US$
Guardar 77,00 US$ (31.83%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs 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 24 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Biological activity:

Tylosin   is a macrolide antibiotic found naturally as a fermentation product of Streptomyces fradiae. Tylosin exerts potent antimicrobial activity against Gram-positive bacteria. Tylosin is widely used as a feed additive for promoting animal growth. Tylosin is used for veterinary purposes against bacterial dysentery and respiratory diseases in poultry, pigs and cattle

Specifications

Sinónimos
Antibiotic obtained from cultures of Streptomyces fradiae, or the same substance produced by any other means | TYLOSIN [MI] | SR-05000002057-3 | TYLOSIN (USP-RS) | 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-
Especificaciones y pureza
10mM in DMSO
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores
Sonrisas canónicasCCC1C(C=C(C=CC(=O)C(CC(C(C(C(CC(=O)O1)O)C)OC2C(C(C(C(O2)C)OC3CC(C(C(O3)C)O)(C)O)N(C)C)O)CC=O)C)C)COC4C(C(C(C(O4)C)O)OC)OC
IUPAC Name2-[(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
InChIKeyWBPYTXDJUQJLPQ-VMXQISHHSA-N
INCHI1S/C46H77NO17/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/h14-15,17-18,24-30,32-33,35-45,50,52-55H,13,16,19-22H2,1-12H3/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-/m1/s1
Isómeros 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
PubChem CID 5280440
Peso molecular 916.12

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
ClaseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides
Direct ParentAminoglycosides
Alternative Parents Macrolides and analogues  Disaccharides  O-glycosyl compounds  Oxanes  Alpha-hydrogen aldehydes  Tertiary alcohols  1,2-aminoalcohols  Trialkylamines  Amino acids and derivatives  Carboxylic acid esters  Cyclic ketones  Secondary alcohols  Lactones  Acetals  Dialkyl ethers  Oxacyclic compounds  Monocarboxylic acids and derivatives  Hydrocarbon derivatives  Organopnictogen compounds  Organic oxides  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Aminoglycoside core - Macrolide - Disaccharide - Glycosyl compound - O-glycosyl compound - Oxane - Alpha-hydrogen aldehyde - Tertiary alcohol - 1,2-aminoalcohol - Amino acid or derivatives - Carboxylic acid ester - Ketone - Lactone - Cyclic ketone - Secondary alcohol - Tertiary aliphatic amine - Tertiary amine - Acetal - Organoheterocyclic compound - Ether - Monocarboxylic acid or derivatives - Dialkyl ether - Oxacycle - Carboxylic acid derivative - Organopnictogen compound - Carbonyl group - Alcohol - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organic nitrogen compound - Amine - Aldehyde - Aliphatic heteromonocyclic compound
DescripciónThis 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 Macrolides and lactone polyketides
Estructura 3D
Modelo de Estructura Química Interactiva





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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:
Propiedades químicas y físicas
Peso molecular916.100 g/mol
XLogP31.000
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count18
Rotatable Bond Count13
Exact Mass915.519 Da
Monoisotopic Mass915.519 Da
Topological Polar Surface Area239.000 Ų
Heavy Atom Count64
Formal Charge0
Complexity1560.000
Isotope Atom Count0
Defined Atom Stereocenter Count21
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count2
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds2
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Linsen Ruan, Kaiyu Ye, Zhicheng Wang, Anqi Xiong, Rong Qiao, Jibin Zhang, Zhiyong Huang, Minmin Cai, Chan Yu.  (2023)  Characteristics of gut bacterial microbiota of black soldier fly (Diptera: Stratiomyidae) larvae effected by typical antibiotics.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:38154153] [10.1016/j.ecoenv.2023.115861]
2. Song Lianjun, Wang Youyi, Li Qingyue, Wang Jinkui, Gao Tian, An Zhaohuan, Liu Qinfang, Mao Yexuan, Bu Tong, Huang Xianqing, Ma Yan, Wang Zhanhui, Zhang Xiya.  (2023)  Production of monoclonal antibody against tylosin and tilmicosin with homogeneous cross-reactivity and its application in lateral flow immunoassay.  MICROCHIMICA ACTA,  191  (1): (1-12).  [PMID:38114730] [10.1007/s00604-023-06132-z]
3. Xin-Yu Liu, Xiao-Yun Gu, Chen Liu, Lanre Anthony Gbadegesin, Yang He, Jian-Qiang Zhang.  (2023)  Field migration of veterinary antibiotics via surface runoff from chicken-raising orchard in responding to natural rainfalls.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:37967624] [10.1016/j.scitotenv.2023.168527]
4. Wenjing Li, Yang Li, Junlong Cai, Yue Wang, Yanan Liu, Hankun Hu, Liang Liu.  (2023)  Simultaneous Quantification of Seven Antifungal Agents in Human Serum Using Liquid Chromatography-Tandem Mass Spectrometry.  Pharmaceuticals,  16  (11): (1537).  [PMID:38004403] [10.3390/ph16111537]
5. Xiangdong Zhang, Jian Zhang, Bowen Hou, Xueying Yang, Junlian Ren, Chen Shao.  (2023)  Efficient removal of oxytetracycline hydrochloride by ZIF-67 coated hollow spherical CuS (CuS-PVP@ZIF-67) under the synergistic effect of adsorption and PMS activation.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2023.158663]
6. Yu Wang, Jin-Yi Yang, Ying He, Lu Li, Jian-Xin Huang, Yuan-Xin Tian, Hong Wang, Zhen-Lin Xu, Yu-Dong Shen.  (2021)  Development of Time-Resolved Fluorescence Immunochromatographic Assays for Simultaneously Detecting Tylosin and Tilmicosin in Milk in Group-Screening Manner.  Foods,  10  (8): (1838).  [PMID:34441616] [10.3390/foods10081838]
7. Zaiming Chen, Jianfei Wang, Yuefeng Wang, Bing Li, Meizhen Wang.  (2021)  Rapid formation of pyrogenic char (biochar) with high and low sorption capacity towards organic chemicals.  ENVIRONMENTAL POLLUTION,      [PMID:33460877] [10.1016/j.envpol.2021.116472]
8. Yanmei Sun, Yajie Guo, Mingming Shi, Tianlei Qiu, Min Gao, Shulei Tian, Xuming Wang.  (2020)  Effect of antibiotic type and vegetable species on antibiotic accumulation in soil-vegetable system, soil microbiota, and resistance genes.  CHEMOSPHERE,      [PMID:33297095] [10.1016/j.chemosphere.2020.128099]
9. Guanqiong Na, Xiaofei Hu, Yaning Sun, Sharon Kwee, Guangxu Xing, Yunrui Xing, Gaiping Zhang.  (2020)  A highly sensitive monoclonal antibody−based paper sensor for simultaneously detecting valnemulin and tiamulin in porcine liver.  JOURNAL OF FOOD SCIENCE,  85  (6): (1681-1688).  [PMID:32418205] [10.1111/1750-3841.15136]
10. Shanshan Wang, Nana Xue, Wenfeng Li, Daoyong Zhang, Xiangliang Pan, Yongming Luo.  (2019)  Selectively enrichment of antibiotics and ARGs by microplastics in river, estuary and marine waters.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:31796269] [10.1016/j.scitotenv.2019.134594]
11. 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]
12. Xuejun Cui, Rongguo Li, Xiaofei Liu, Jingfeng Wang, Xueqi Leng, Xiaolei Song, Qianqian Pei, Yu Wang, Su Liu, Jiadong Huang.  (2017)  Low-background and visual detection of antibiotic based on target-activated colorimetric split peroxidase DNAzyme coupled with dual nicking enzyme signal amplification.  ANALYTICA CHIMICA ACTA,      [PMID:29149989] [10.1016/j.aca.2017.10.009]
13. Wei-Chuang Kong, Chen-Chen Li, Ai-Hong Zhang, Xin-Long Li, Qian-Rui Gong, Bing-Tan Jin, Xiao-Juan Jia, Xu-Ying Liu, Yan-Fei Kang.  (2024)  A colorimetric-aptamer-based assay for the determination of enrofloxacin through triggering the aggregation of gold nanoparticles.  Analytical Methods,      [PMID:39311407] [10.1039/D4AY01259C]
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18. Yi Zhang, Zhaoju Wu, Haizhu Shi, Yang Xie, Ming-Yu Wu, Chungu Zhang, Shun Feng.  (2022)  Copper mediated molecularly imprinted polymers for fast recognizing tylosin.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:35219066] [10.1016/j.jpba.2022.114674]
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23. Qiaonan Wang, Mingyao Yu, Han Dong, Jingjing Duan, Yanxia Ding, Jinxiao Wang, Yujie Guo, Yaqian Huang, Tao Zhang, Xiaoxing Dong, Fengzhi Piao, Zhixin Guo.  (2026)  Abscisic acid confers antibiotic stress tolerance in cucumber by alleviating antibiotic phytotoxicity and decreasing the levels of antibiotic and antibiotic resistance genes.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:41506203] [10.1016/j.jhazmat.2026.141060]
24. Guomin Li, Zhuoyang Li, Liqiu Zhang, Pinliang Lai, Bing Wang.  (2026)  Universality of Tm-Doped g─C3N4 for Photocatalytic Activation of Persulfate in Organic Pollutant Degradation.  ChemistrySelect,  11  (11): (e07294).  [PMID:] [10.1002/slct.202507294]
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