5-Bromo-2′-deoxyuridine(BrdU) - ≥99% , CAS No.59-14-3

CAS: 59-14-3 Cat. No.: B110731 Peso molecular: 307.10 Beilstein Registry Number: 30395 Número EC: 200-415-9
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
BrdU | 5-Bromo-2'-deoxyuridine, >=99.0% (HPLC) | MLS002153366 | WOVKYSAHUYNSMH-RRKCRQDMSA-N | Broxuridina [INN-Spanish] | NCGC00090770-04 | STL530083 | 5-bromo-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione |
Storage
Almacenar a -20°C,cargado con argón
Shipped In
Hielera + almohadillas de hielo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
250mg
B110731-250mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
9,90US$
1g
B110731-1g
1
19,90US$
5g
B110731-5g
3
59,90US$
25g
B110731-25g
1
199,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Almacenar a -20°C,cargado con argón Ships Hielera + almohadillas de hielo 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 12 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

la 5-bromo-2'-desoxiuridina es un análogo de la timidina. Es útil para el estudio de la síntesis del ADN, donde se incorpora al ADN en lugar de la timidina. la 5-bromo-2'-desoxiuridina puede utilizarse para marcar el ADN. El ADN resultante puede utilizarse junto con el anticuerpo monoclonal BrdU para el análisis inmunohistoquímico de la proliferación celular.
Un análogo de la timidina útil para el marcaje del ADN

Specifications

Sinónimos
BrdU | 5-Bromo-2'-deoxyuridine, >=99.0% (HPLC) | MLS002153366 | WOVKYSAHUYNSMH-RRKCRQDMSA-N | Broxuridina [INN-Spanish] | NCGC00090770-04 | STL530083 | 5-bromo-1-[(2R, 4S, 5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1, 2, 3, 4-tetrahydropyrimidine-2, 4-dione |
Especificaciones y pureza
≥99%
Mecanismos bioquímicos y fisiológicos
la 5-bromo-2′-desoxiuridina (5-BrdU) es un análogo de la timidina que se incorpora al ADN. el 5-BrdU se utiliza de forma rutinaria y generalizada para medir la síntesis de ADN y etiquetar las células en división. Por consiguiente, el 5-BrdU se utiliza par
Condiciones de almacenamiento de almacenamiento
Almacenar a -20°C, cargado con argón
Enviado en
Hielera + almohadillas de hielo
Nota
Siempre que sea posible, prepare y utilice las soluciones el mismo día. Sin embargo, si necesita preparar soluciones madre con antelación, le recomendamos que almacene la solución como alícuotas en viales herméticamente cerrados a -20°C. Por lo general, podrán utilizarse durante un mes. Antes de su uso, y antes de abrir el vial, le recomendamos que deje que el producto se equilibre a temperatura ambiente durante al menos 1 hora. ¿Necesita más consejos sobre solubilidad, uso y manipulación? Visite nuestra página de preguntas frecuentes (FAQ) para obtener más información.
Pureza
≥99%
Nombres e identificadores
Pubchem Sid504750990
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750990
Sonrisas canónicasC1C(C(OC1N2C=C(C(=O)NC2=O)Br)CO)O
IUPAC Name5-bromo-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione
InChIKeyWOVKYSAHUYNSMH-RRKCRQDMSA-N
INCHI1S/C9H11BrN2O5/c10-4-2-12(9(16)11-8(4)15)7-1-5(14)6(3-13)17-7/h2,5-7,13-14H,1,3H2,(H,11,15,16)/t5-,6+,7+/m0/s1
Isómeros SMILES C1[C@@H]([C@H](O[C@H]1N2C=C(C(=O)NC2=O)Br)CO)O
WGK Alemania 2
RTECS YU7350000
Peso molecular 307.10
Beilstein 30395
Reaxy-Rn 24730832
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24730832&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
SuperclassNucleosides, nucleotides, and analogues
ClasePyrimidine nucleosides
SubclassPyrimidine 2'-deoxyribonucleosides
Intermediate Tree Nodes Not available
Direct ParentPyrimidine 2'-deoxyribonucleosides
Alternative Parents Pyrimidones  Halopyrimidines  Hydroxypyrimidines  Aryl bromides  Hydropyrimidines  Tetrahydrofurans  Heteroaromatic compounds  Secondary alcohols  Oxacyclic compounds  Azacyclic compounds  Organic oxides  Hydrocarbon derivatives  Organobromides  Organonitrogen compounds  Organopnictogen compounds  Primary alcohols  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyrimidine 2'-deoxyribonucleoside - Halopyrimidine - Hydroxypyrimidine - Pyrimidone - Aryl bromide - Aryl halide - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Tetrahydrofuran - Secondary alcohol - Oxacycle - Organoheterocyclic compound - Azacycle - Alcohol - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.
External Descriptors pyrimidine 2'-deoxyribonucleoside
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
AR Tclin Androgen Receptor (11781 Activities)
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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
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MAOA Tclin Monoamine oxidase A (11911 Activities)
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CXCL8 Tchem Interleukin-8 (642 Activities)
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TK1 Tchem Thymidine kinase, cytosolic (627 Activities)
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ARSA Tbio Cerebroside-sulfatase (655 Activities)
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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
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HT-29 (80576 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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SNB-19 (46794 Activities)
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Objetivos asociados (no humanos)
TK Thymidine kinase (276 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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ddn Putative uncharacterized protein (49 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.

16 results found

Lot NumberCertificate TypeFechaArticulo
C2625303Certificate of AnalysisMar 02, 2026 B110731
C2625304Certificate of AnalysisMar 02, 2026 B110731
C2625315Certificate of AnalysisMar 02, 2026 B110731
C2625316Certificate of AnalysisMar 02, 2026 B110731
H2204353Certificate of AnalysisFeb 04, 2026 B110731
H2204354Certificate of AnalysisFeb 04, 2026 B110731
F2509101Certificate of AnalysisJun 17, 2025 B110731
D2518091Certificate of AnalysisApr 27, 2025 B110731
H2204355Certificate of AnalysisMay 20, 2024 B110731
H2204356Certificate of AnalysisMay 20, 2024 B110731
H1801129Certificate of AnalysisNov 08, 2023 B110731
L2107288Certificate of AnalysisSep 20, 2023 B110731
F2124201Certificate of AnalysisMar 16, 2023 B110731
F2124200Certificate of AnalysisMar 09, 2023 B110731
I2003088Certificate of AnalysisJul 14, 2022 B110731
I2003086Certificate of AnalysisJul 14, 2022 B110731

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Propiedades químicas y físicas
SolubilidadSoluble in water (10 mg/mL), NH4OH (0.1 M) at 20 °C, DMF, DMSO, and sodium hydroxide.
SensibilidadLight sensitive;Air sensitive
Rotación específica [α]22 ° (C=1, H2O)
Punto de fusión (°C)191-194°C
Peso molecular307.100 g/mol
XLogP3-0.300
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count2
Exact Mass305.985 Da
Monoisotopic Mass305.985 Da
Topological Polar Surface Area99.100 Ų
Heavy Atom Count17
Formal Charge0
Complexity386.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Liu Xing-Yang, Wang Ke, Deng Xian-Hua, Wei Yi-Hua, Guo Rui, Liu Sui-Feng, Zhu Yi-Fan, Zhong Jia-Jun, Zheng Jing-Yuan, Wang Meng-Dan, Ye Qiu-Hong, He Jian-Quan, Guo Kai-Hang, Zhu Jun-Rong, Huang Shu-Qiong, Chen Ze-Xu, Lv Chong-Shan, Wen Lei.  (2023)  Amelioration of olfactory dysfunction in a mouse model of Parkinson’s disease via enhancing GABAergic signaling.  Cell and Bioscience,  13  (1): (1-20).  [PMID:37270503] [10.1186/s13578-023-01049-9]
2. Chuanzhuo Wang, He Xin, Guangxin Yan, Zhaoyu Liu.  (2023)  NONHSAG028908.3 sponges miR‑34a‑5p to promote growth of colorectal cancer via targeting ALDOA.  ONCOLOGY REPORTS,  49  (5): (1-14).  [PMID:36929422] [10.3892/or.2023.8526]
3. Xiaosong Wei, Beibei Wang, Zixin Wu, Xiaoming Yang, Yufeng Guo, Yang Yang, Zhiwei Fang, Chengzhi Yi, Liuhui Zhang, Xin Fan, Lirong Zhang, Dongkui Song.  (2023)  WD repeat protein 54-mediator of ErbB2-driven cell motility 1 axis promotes bladder cancer tumorigenesis and metastasis and impairs chemosensitivity.  CANCER LETTERS,      [PMID:36627049] [10.1016/j.canlet.2023.216058]
4. Hanwen Liu, Ying Liu, Ting Zhou, Penghui Zhou, Jianguo Li, Anping Deng.  (2022)  Ultrasensitive and Specific Detection of Anticancer Drug 5-Fluorouracil in Blood Samples by a Surface-Enhanced Raman Scattering (SERS)-Based Lateral Flow Immunochromatographic Assay.  MOLECULES,  27  (13): (4019).  [PMID:35807264] [10.3390/molecules27134019]
5. Ting Zhou, Guangzhao He, Changjia Hu, Kang Wu, Ying Liu, Jianguo Li, Anping Deng.  (2022)  Development of a highly sensitive and specific monoclonal antibody-based ELISA coupled with immuno-affinity extraction for the detection of anticancer drug 5-fluorouracil in blood samples.  TALANTA,      [PMID:35696979] [10.1016/j.talanta.2022.123655]
6. Shuhui Wang, Xueling Su, Lina Xu, Cheng Chang, Yu Yao, Sumra Komal, Xuexiang Cha, Mingxi Zang, Xinshou Ouyang, Lirong Zhang, Shengna Han.  (2020)  Glycogen synthase kinase-3β inhibition alleviates activation of the NLRP3 inflammasome in myocardial infarction.  JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY,      [PMID:32991876] [10.1016/j.yjmcc.2020.09.009]
7. Zhang Yaqiong, Gao Lingyue, Cheng Zhihua, Cai Jiayi, Niu Yixuan, Meng Weihong, Zhao Qingchun.  (2016)  Kukoamine A Prevents Radiation-Induced Neuroinflammation and Preserves Hippocampal Neurogenesis in Rats by Inhibiting Activation of NF-κB and AP-1.  NEUROTOXICITY RESEARCH,  31  (2): (259-268).  [PMID:27815817] [10.1007/s12640-016-9679-4]
8. Xin‑Yu Wu, Rui‑Tai Fan, Xin‑Hui Yan, Jing Cui, Jun‑Ling Xu, Hao Gu, Yong‑Ju Gao.  (2014)  Endoplasmic reticulum stress protects human thyroid carcinoma cell lines against ionizing radiation-induced apoptosis.  Molecular Medicine Reports,  11  (3): (2341-2347).  [PMID:25405642] [10.3892/mmr.2014.2956]
9. Guoqiang Xing, Hekai Chen, Zhiyue Guo, Yu Cui, Yongyuan Li, Jianwei Shen.  (2024)  OTUD6B promotes cholangiocarcinoma growth by regulating STAT3 phosphorylation through deubiquitination of PTK2.  CELL BIOLOGY INTERNATIONAL,      [PMID:39192576] [10.1002/cbin.12234]
10. Ke Wang, Xing-Yang Liu, Sui-Feng Liu, Xiao-Xia Wang, Yi-Hua Wei, Jun-Rong Zhu, Jing Liu, Xiu Qin Xu, Lei Wen.  (2024)  Rbm24/Notch1 signaling regulates adult neurogenesis in the subventricular zone and mediates Parkinson-associated olfactory dysfunction.  Theranostics,      [PMID:39113792] [10.7150/thno.96045]
11. Huang Zhengyuan, Ren Zhongyu, Wang Sanwang, Xiao Ling, Ling Yipeng, Xie Yinping, Wang Gaohua, Zhou Benhong.  (2025)  Urolithin A alleviates schizophrenic-like behaviors and cognitive impairment in rats through modulation of neuroinflammation, neurogenesis, and synaptic plasticity.  Scientific Reports,  15  (1): (1-15).  [PMID:40140679] [10.1038/s41598-025-93554-9]
12. Yu Liang, Jie Gao, Litian Han, Yao Zhou, Qianqian Li, Fei Pei, Zhi Chen, Peng Fei, Yufeng Zhang, Huan Liu.  (2026)  A p63-dependent molecular switch directs epithelial fate to form a specialized seal at the tooth-gingiva interface.  Cell Reports,  45  (2):   [PMID:41686636] [10.1016/j.celrep.2026.116981]
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