Cytidine 5'-monophosphate - 10mM in Water , CAS No.63-37-6

CAS: 63-37-6 Cat. No.: C427232 Peso molecular: 323.2 Beilstein Registry Number: 46982 Número EC: 200-556-6
Disponible para pedir
GRADE & PURITY 10mM in Water
Synonyms
5'-CYTIDYLIC ACID|Cytidine 5'-monophosphate|63-37-6|cytidylic acid|Cytidine monophosphate|Cytidine-5'-monophosphate|5'-CMP|cytidylate|Cytidine 5'-phosphate|CMP (nucleotide)|Cytidine 5'-phosphoric acid|Cytidine 5'-monophosphoric acid|((2R,3S,4R,5R)-5-(4-am
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
C427232-1ml
1
144,90US$
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Why this grade

10mM in Water 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.

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Literature proof

Cited in 25 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
5'-CYTIDYLIC ACID | Cytidine 5'-monophosphate | 63-37-6 | cytidylic acid | Cytidine monophosphate | Cytidine-5'-monophosphate | 5'-CMP | cytidylate | Cytidine 5'-phosphate | CMP (nucleotide) | Cytidine 5'-phosphoric acid | Cytidine 5'-monophosphoric acid | ((2R, 3S, 4R, 5R)-5-(4-am
Especificaciones y pureza
10mM in Water
Mecanismos bioquímicos y fisiológicos
Nucleoside monophosphate used as a substrate of uridine monophosphate (UMP)/cytidine monophosphate (CMP) kinase (EC 2.7.4.4) to form CDP which upon phosphorylation to CTP supports DNA and RNA biosynthesis.
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 canónicasC1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)O)O)O
IUPAC Name[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate
InChIKeyIERHLVCPSMICTF-XVFCMESISA-N
INCHI1S/C9H14N3O8P/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(20-8)3-19-21(16,17)18/h1-2,4,6-8,13-14H,3H2,(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
Isómeros SMILES C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)O)O)O
WGK Alemania 3
RTECS HA3980000
Peso molecular 323.2
Beilstein 46982
Reaxy-Rn 14609599
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=14609599&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 nucleotides
SubclassPyrimidine ribonucleotides
Intermediate Tree Nodes Not available
Direct ParentPyrimidine ribonucleoside monophosphates
Alternative Parents Pentose phosphates  Glycosylamines  Monosaccharide phosphates  Monoalkyl phosphates  Aminopyrimidines and derivatives  Pyrimidones  Imidolactams  Hydropyrimidines  Heteroaromatic compounds  Tetrahydrofurans  Secondary alcohols  1,2-diols  Oxacyclic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Pyrimidine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Tetrahydrofuran - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Oxacycle - Organoheterocyclic compound - Azacycle - Organopnictogen compound - Amine - Alcohol - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Primary amine - Organic oxygen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pyrimidine ribonucleoside monophosphates. These are pyrimidine ribobucleotides with monophosphate group linked to the ribose moiety.
External Descriptors Ribonucleotides
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
UCK2 Tbio Uridine-cytidine kinase 2 (58 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCRF-CEM (65223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RNASE1 Tchem Ribonuclease pancreatic (45 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UMPS Tclin Uridine 5'-monophosphate synthase (20 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CMPK1 Tchem UMP-CMP kinase (152 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
St6gal1 CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,6-sialyltransferase (61 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
St3gal3 CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
B16 (5829 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L1210 (27553 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L1210/ara C (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ompdc Orotidine phosphate decarboxylase (9 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
pyrF Orotidine 5'-phosphate decarboxylase (39 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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
Rotación específica [α]9.8 ° (C=1, 0.5mol/L Na2HPO4)
Peso molecular323.200 g/mol
XLogP3-3.400
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count8
Rotatable Bond Count4
Exact Mass323.052 Da
Monoisotopic Mass323.052 Da
Topological Polar Surface Area175.000 Ų
Heavy Atom Count21
Formal Charge0
Complexity531.000
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 Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Yujuan Ren, Kaiwen Zhao, Guangyao Wu, Lianghai Hu.  (2023)  Highly Ordered Assembly of Templates on Molecular Imprinting toward Phosphorylated Compounds for Improved Performance.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.3c02841]
2. Lai Liang, Zhang Mengyun, Liu Chusheng, Qu Jiahuan, Xu Dongsheng, Jiang Zhengjin.  (2023)  A comprehensive evaluation of a polymeric zwitterionic hydrophilic monolith for nucleotide separation.  ANALYTICAL SCIENCES,      [PMID:37843729] [10.1007/s44211-023-00430-5]
3. Tiantian Tang, Min Zhang, Yaping Liu.  (2023)  Valorization of meat and bone residue by ultrasound and high voltage electrostatic field assisted two-stage enzymatic hydrolysis: Nutritional characteristics and flavor analysis.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2023.103203]
4. Xu Shichao, Wu Haifeng, Liu Siyuan, Du Peidong, Wang Hui, Yang Haijun, Xu Wenjie, Chen Shuangming, Song Li, Li Jikun, Shi Xinghua, Wang Zhen-Gang.  (2023)  A supramolecular metalloenzyme possessing robust oxidase-mimetic catalytic function.  Nature Communications,  14  (1): (1-14).  [PMID:37419896] [10.1038/s41467-023-39779-6]
5. Peidong Du, Yanzhe Shen, Baoli Zhang, Shan Li, Minzheng Gao, Ting Wang, Xiaokang Ding, Bingran Yu, Zhen-Gang Wang, Fu-Jian Xu.  (2023)  A H2O2-Supplied Supramolecular Material for Post-irradiated Infected Wound Treatment.  Advanced Science,  10  (9): (2206851).  [PMID:36709479] [10.1002/advs.202206851]
6. Yuqin Wang, Pingping Fan, Shanyu Zhang, Liying Wang, Xinyue Li, Wendong Jia, Yao Liu, Kefan Wang, Xiaoyu Du, Panke Zhang, Shuo Huang.  (2022)  Discrimination of Ribonucleoside Mono-, Di-, and Triphosphates Using an Engineered Nanopore.  ACS Nano,      [PMID:36475606] [10.1021/acsnano.2c09662]
7. Yafei Hou, Xiaodan Pei, Yuancheng Wang, Luyuan Zhang, Xiaohui Wei, Hongyan Mao, Wuduo Zhao, Shusheng Zhang, Wenfen Zhang.  (2022)  Selective Detection of Nucleotides in Infant Formula Using an N-Rich Covalent Triazine Porous Polymer.  Nanomaterials,  12  (13): (2213).  [PMID:35808047] [10.3390/nano12132213]
8. Jianghong Wu, Min Zhang, Lihui Zhang, Yaping Liu.  (2022)  Effect of ultrasound combined with sodium bicarbonate pretreatment on the taste and flavor of chicken broth.  JOURNAL OF FOOD PROCESS ENGINEERING,  46  (6): (e14072).  [PMID:] [10.1111/jfpe.14072]
9. Hui Hou, Chang Liu, Xiaoshuo Lu, Donglu Fang, Qiuhui Hu, Yuyu Zhang, Liyan Zhao.  (2021)  Characterization of flavor frame in shiitake mushrooms (Lentinula edodes) detected by HS-GC-IMS coupled with electronic tongue and sensory analysis: Influence of drying techniques.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2021.111402]
10. Chen Pengfei, Wu Jing, Zhou Lei, Pu Qiaosheng.  (2021)  In situ controllable synthesis of Schiff base networks porous polymer coatings for open-tubular capillary electrochromatography.  MICROCHIMICA ACTA,  188  (3): (1-9).  [PMID:33586055] [10.1007/s00604-021-04740-1]
11. Mei He, Ma Yange, Wu Huimin, Wang Xuedong.  (2021)  Fluorescent and visual assay of H2O2 and glucose based on a highly sensitive copper nanoclusters-Ce(III) fluoroprobe.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  413  (8): (2135-2146).  [PMID:33511458] [10.1007/s00216-021-03181-2]
12. Hongying Li, Qiujin Zhu, Rui Chang, Ke Hu, Xuling Zhu, Aqi Xu, Shitao Xu, Pengyu Tang.  (2020)  Effects of Dietary 5′-CMP on Neu5Gc Contents in the Muscle and Viscera of Xiang Pigs.  JOURNAL OF FOOD PROTECTION,      [PMID:33393618] [10.4315/JFP-20-191]
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16. Ruiyong Wang, Xiaogai Wang, Zhigang Li, Yuanzhe Xie, Lingling Yang, Jie Shi, Junbiao Chang.  (2014)  Study on the interaction between bovine serum albumin and 4′-azido-2′-deoxyfluoroarabinocytidine or analogs by spectroscopy and molecular modeling.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:24971719] [10.1016/j.saa.2014.05.090]
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19. Zhongshuai Zhao, Ran Li, Ying Zhu, Zhongde Liu.  (2024)  Headspace separation combined fluorescence detection of hydrogen sulfide with silver-sensitized lanthanide coordination polymer via a simple self-made device.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.111617]
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