Cloruro de Fmoc - ≥98% , CAS No.28920-43-6

CAS: 28920-43-6 Cat. No.: F106533 Peso molecular: 258.7 Beilstein Registry Number: 2279177 Número EC: 249-313-6
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
Fmoc-Cl | Cloruro de Fmoc | (9h-fluoren-9-il)metil carbonocloridato | Cloruro de 9-Fluorenilmetoxicarbonilo | Cloroformato de 9-Fluorenilmetilo | Cloruro de Fmoc | Cloroformato de 9H-Fluoren-9-ilmetilo | Ácido carbonoclorídico, éster de 9H-fluoren-9-ilmet
Storage
Conservar a 2-8°C,cargado con argón
Shipped In
Hielo húmedo
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
F106533-1g
2
9,90US$
5g
F106533-5g
2
14,90US$
10g
F106533-10g
2
19,90US$
25g
F106533-25g
1
29,90US$
100g
F106533-100g
3
59,90US$
500g
F106533-500g
1
179,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Conservar a 2-8°C,cargado con argón Ships Hielo húmedo 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 20 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

El cloruro de Fmoc es un agente derivatizante.
Agente derivatizante de aminoácidos para el análisis de HLPC. Reactivo N-protector para síntesis de péptidos y oligonucleótidos. Reactivo para la protección de grupos amino utilizado recientemente en la síntesis de un análogo bicíclico de la prolina. Reactivo para la derivatización de aminoácidos para el análisis de aminoácidos por HPLC y para la preparación de aminoácidos N-Fmoc para la síntesis de péptidos en fase sólida.

Specifications

Sinónimos
Fmoc-Cl | Cloruro de Fmoc | (9h-fluoren-9-il)metil carbonocloridato | Cloruro de 9-Fluorenilmetoxicarbonilo | Cloroformato de 9-Fluorenilmetilo | Cloruro de Fmoc | Cloroformato de 9H-Fluoren-9-ilmetilo | Ácido carbonoclorídico, éster de 9H-fluoren-9-ilmet
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C, cargado con argón
Enviado en
Hielo húmedo
Pureza
≥98%
Nombres e identificadores
Sonrisas canónicasC1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)Cl
IUPAC Name9H-fluoren-9-ylmethyl carbonochloridate
InChIKeyIRXSLJNXXZKURP-UHFFFAOYSA-N
INCHI1S/C15H11ClO2/c16-15(17)18-9-14-12-7-3-1-5-10(12)11-6-2-4-8-13(11)14/h1-8,14H,9H2
Isómeros SMILES C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)Cl
WGK Alemania 3
RTECS LQ6250000
Número ONU 3261
Peso molecular 258.7
Beilstein 2279177
Reaxy-Rn 2279177
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2279177&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
SuperclassBenzenoids
ClaseFluorenes
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentFluorenes
Alternative Parents Organic carbonic acids and derivatives  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Fluorene - Carbonic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Carbonyl group - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as fluorenes. These are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

43 results found

Lot NumberCertificate TypeFechaArticulo
I2221343Certificate of AnalysisMar 18, 2026 F106533
C2616703Certificate of AnalysisMar 06, 2026 F106533
C2616702Certificate of AnalysisMar 06, 2026 F106533
C2616690Certificate of AnalysisMar 06, 2026 F106533
D2418075Certificate of AnalysisJan 20, 2026 F106533
A2410017Certificate of AnalysisOct 11, 2025 F106533
J2514704Certificate of AnalysisSep 28, 2025 F106533
J2514406Certificate of AnalysisSep 28, 2025 F106533
C2205152Certificate of AnalysisSep 08, 2025 F106533
D2303937Certificate of AnalysisJun 17, 2025 F106533
I2525059Certificate of AnalysisApr 09, 2025 F106533
E2506156Certificate of AnalysisApr 09, 2025 F106533
E2506155Certificate of AnalysisApr 09, 2025 F106533
E2506147Certificate of AnalysisApr 09, 2025 F106533
E2506153Certificate of AnalysisApr 09, 2025 F106533
L2409422Certificate of AnalysisNov 19, 2024 F106533
L2425049Certificate of AnalysisNov 19, 2024 F106533
L2425050Certificate of AnalysisNov 19, 2024 F106533
L2425051Certificate of AnalysisNov 19, 2024 F106533
L2425052Certificate of AnalysisNov 19, 2024 F106533
I2221344Certificate of AnalysisJun 12, 2024 F106533
E2429367Certificate of AnalysisMay 10, 2024 F106533
E2429368Certificate of AnalysisMay 10, 2024 F106533
G2408601Certificate of AnalysisApr 12, 2024 F106533
G2402225Certificate of AnalysisApr 12, 2024 F106533
G2402246Certificate of AnalysisApr 12, 2024 F106533
G2402247Certificate of AnalysisApr 12, 2024 F106533
D2303905Certificate of AnalysisMar 09, 2023 F106533
D2303903Certificate of AnalysisMar 09, 2023 F106533
C2130137Certificate of AnalysisJan 11, 2023 F106533
C2130138Certificate of AnalysisJan 11, 2023 F106533
C2130139Certificate of AnalysisJan 11, 2023 F106533
K2019234Certificate of AnalysisSep 21, 2022 F106533
H2210034Certificate of AnalysisAug 16, 2022 F106533
I2222139Certificate of AnalysisAug 15, 2022 F106533
B2303971Certificate of AnalysisAug 15, 2022 F106533
B2418180Certificate of AnalysisAug 15, 2022 F106533
L2222023Certificate of AnalysisAug 15, 2022 F106533
C2418082Certificate of AnalysisAug 15, 2022 F106533
I2221341Certificate of AnalysisAug 15, 2022 F106533
G2311073Certificate of AnalysisAug 15, 2022 F106533
F2010100Certificate of AnalysisApr 25, 2022 F106533
C2205153Certificate of AnalysisMar 23, 2022 F106533

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Propiedades químicas y físicas
SolubilidadSoluble in dioxane.
SensibilidadHygroscopic,Heat Sensitive
Punto de fusión (°C)61.0 - 65.0 °C
Peso molecular258.700 g/mol
XLogP34.300
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count3
Exact Mass258.045 Da
Monoisotopic Mass258.045 Da
Topological Polar Surface Area26.300 Ų
Heavy Atom Count18
Formal Charge0
Complexity296.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
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
A bridge to protein science——Aladdin@Polypeptide
Amino Acid Oxidases: Oxygen-Dependent Oxidative Deamination Systems and Their Analytical and Applied Uses
Roles of the Carboxypeptidase Family in Protein C-Terminal Processing and Experimental Analysis
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Understanding Cbz (Benzyloxycarbonyl): Selection Logic and Practical Value of a Classical Amino Protecting Group
Reconsidering N-Acyl Amino Protecting Groups: Deprotection Differences, Strategic Roles, and Experimental Selection of Ac, Bz, and Tfa
Technical Comparison and Method Selection for Hydroxyproline Determination
Selection Logic for Hydroxyl Protecting Groups: Deprotection Conditions, Task Differentiation, and Orthogonal Combination Design
Decision Logic for Peptide Synthesis Routes: Applicability and Criteria for Choosing among SPPS, LPPS, and Recombinant Expression
Selection Logic for the Teoc Amino Protecting Group: From Fluoride-Triggered Deprotection to Orthogonal Protecting-Group Design
Boc₂O Selection Cannot Be Judged by Protection Installation Alone: Experimental Decision-Making from Substrate Nucleophilicity and Medium Effects to Deprotection Pathways
Methods and Applications for the Determination of Amino Acid Content and Composition
Experimental Selection Logic for Pentafluorophenyl-Based Systems: Practical Judgment from Active Esters and Pre-Activated Monomers to Downstream Transformations
Experimental Assessment of Fmoc Introduction Routes: Impurity Profile Differences, Raw Material Carryover, and Quality Control
How to Troubleshoot Abnormal Impurities in Peptide Synthesis? Locating Process Issues Through Amino-Related Side Reactions
Peptide Intermediates Difficult to Dissolve and Separate? Route Design and Workup Strategies for Tag-Assisted Liquid-Phase Peptide Synthesis (TAG-LPPS)
What Are Polyamines? Structural Features, Classification and Representative Compounds, Applications, and Synthetic Strategies
Citations of This Product
Referencias
1. Hang Xu, Mengfei Zheng, Chenguang Yang, Kun Wang, Zheng Lv, Zhilin Liu, Zhaohui Tang, Xuesi Chen.  (2023)  Azo-based hypoxic-activated 6-diazo-5-oxo-L-norleucine (DON) prodrug combined with vascular disrupting agent nanoparticles for tumor-selective glutamine metabolism blockade.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.148281]
2. Biao Yan, Yumiao Sun, Kaiyu Fu, Yindan Zhang, Lei Lei, Jun Men, Yongyong Guo, Shengmin Wu, Jian Han, Bingsheng Zhou.  (2023)  Effects of glyphosate exposure on gut–liver axis: Metabolomic and mechanistic analysis in grass carp (Ctenopharyngodon idellus).  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:37544446] [10.1016/j.scitotenv.2023.166062]
3. Qian Hai-Long, Liu Fang, Liu Xue, Yang Cheng, Yan Xiu-Ping.  (2021)  Chiral covalent organic framework-monolith as stationary phase for high-performance liquid chromatographic enantioseparation of selected amino acids.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  414  (18): (5255-5262).  [PMID:34331090] [10.1007/s00216-021-03574-3]
4. Chang Wang, Yike Wu, Sheng Liu, Liang Zhang, Bi-Feng Liu, Xin Liu.  (2020)  Fmoc N-hydroxysuccinimide ester: A facile and multifunctional role in N-glycan analysis.  ANALYTICA CHIMICA ACTA,      [PMID:32928480] [10.1016/j.aca.2020.07.044]
5. Can Wu, Jing Liu, Ziran Zhai, Liqiang Yang, Xuan Tang, Lingzhi Zhao, Keming Xu, Wenying Zhong.  (2020)  Double-crosslinked nanocomposite hydrogels for temporal control of drug dosing in combination therapy.  Acta Biomaterialia,      [PMID:32084599] [10.1016/j.actbio.2020.02.021]
6. Luyao Zhang, Li Chen, Zhiyuan Meng, Ming Jia, Ruisheng Li, Sen Yan, Sinuo Tian, Zhiqiang Zhou, Jinling Diao.  (2019)  Effects of L-Glufosinate-ammonium and temperature on reproduction controlled by neuroendocrine system in lizard (Eremias argus).  ENVIRONMENTAL POLLUTION,      [PMID:31753638] [10.1016/j.envpol.2019.113564]
7. Wu Hao, Guo Ye, Chen Lei, Chen Guiguang, Liang Zhiqun.  (2019)  A Novel Strategy to Regulate 1-Deoxynojirimycin Production Based on Its Biosynthetic Pathway in Streptomyces lavendulae.  Frontiers in Microbiology,      [PMID:31507573] [10.3389/fmicb.2019.01968]
8. Luyao Zhang, Li Chen, Zhiyuan Meng, Wenjun Zhang, Xin Xu, Zikang Wang, Yinan Qin, Yue Deng, Rui Liu, Zhiqiang Zhou, Jinling Diao.  (2019)  Bioaccumulation, behavior changes and physiological disruptions with gender-dependent in lizards (Eremias argus) after exposure to glufosinate-ammonium and l-glufosinate-ammonium.  CHEMOSPHERE,      [PMID:30965253] [10.1016/j.chemosphere.2019.04.007]
9. Luyao Zhang, Jinling Diao, Li Chen, Zikang Wang, Wenjun Zhang, Yao Li, Zhongnan Tian, Zhiqiang Zhou.  (2018)  Hepatotoxicity and reproductive disruption in male lizards (Eremias argus) exposed to glufosinate-ammonium contaminated soil.  ENVIRONMENTAL POLLUTION,      [PMID:30543945] [10.1016/j.envpol.2018.12.004]
10. Tang Lirong, Lin Fengcai, Li Tao, Cai Zhenghan, Hong Biyun, Huang Biao.  (2018)  Design and synthesis of functionalized cellulose nanocrystals-based drug conjugates for colon-targeted drug delivery.  CELLULOSE,  25  (8): (4525-4536).  [PMID:] [10.1007/s10570-018-1904-2]
11. Shengfeng Huang, Ning Gan, Tianhua Li, You Zhou, Yuting Cao, Youren Dong.  (2017)  Electrochemical aptasensor for multi-antibiotics detection based on endonuclease and exonuclease assisted dual recycling amplification strategy.  TALANTA,      [PMID:29310232] [10.1016/j.talanta.2017.10.016]
12. Bo Xing, Honglin Chen, Xiaoming Zhang.  (2017)  Efficient degradation of organic phosphorus in glyphosate wastewater by catalytic wet oxidation using modified activated carbon as a catalyst.  ENVIRONMENTAL TECHNOLOGY,      [PMID:28332926] [10.1080/09593330.2017.1310935]
13. Lirong Tang, Tao Li, Senyang Zhuang, Qilin Lu, Pengfei Li, Biao Huang.  (2016)  Synthesis of pH-Sensitive Fluorescein Grafted Cellulose Nanocrystals with an Amino Acid Spacer.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.6b01124]
14. Zhang Hui, Zhang Ge, Xu Jing-kun, Wen Yang-ping, Ding Wan-chuan, Zhang Jie, Ming Shou-li, Zhen Shi-jie.  (2015)  Electrosynthesis, characterization and optical sensing application of amino acid functionalized polyfluorene.  CHINESE JOURNAL OF POLYMER SCIENCE,  34  (2): (229-241).  [PMID:] [10.1007/s10118-016-1742-3]
15. Kaili Liang, Li Yang, Jiawei Kang, Bo Liu, Ding Zhang, Liyan Wang, Wei Wang, Qing Wang.  (2024)  Improving Treatment for Parkinson's Disease: Harnessing Photothermal and Phagocytosis-Driven Delivery of Levodopa Nanocarriers Across the Blood-Brain Barrier.  Asian Journal of Pharmaceutical Sciences,      [PMID:39640059] [10.1016/j.ajps.2024.100963]
16. Danyi Chen, Rongrong Zhao, Honglin Liu, Hailin Tian, Yiqun Tian, Di Huang, David Johnson, Yingping Huang.  (2025)  Selective photo-Fenton degradation of glyphosate using Schiff base metal complexes: Insights into metal-mediated pathways.  Journal of Cleaner Production,      [PMID:] [10.1016/j.jclepro.2025.144837]
17. Ruili Ma, Weiguo Wu, Yikang Shu, Ran Gao, Ziyu Wang, Daoquan Tang, Yan Du, Shuai Ji.  (2025)  Simultaneous extraction and in situ separation of flavonoids and alkaloids from mulberry leaves using a pH-responsive deep eutectic solvent/water system.  FOOD CHEMISTRY,      [PMID:39884234] [10.1016/j.foodchem.2025.143008]
18. Na Guo, Yi-Wei Jiang, Ping Kou, Zhi-Ming Liu, Thomas Efferth, Yan-Yan Li, Yu-Jie Fu.  (2019)  Application of integrative cloud point extraction and concentration for the analysis of polyphenols and alkaloids in mulberry leaves.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:30771646] [10.1016/j.jpba.2019.02.002]
19. Shuai Yang, Lin Zhang, Yibing Sun, Zhichao Yang, Hongchao Li.  (2025)  Nonradical degradation of phosphonates to orthophosphate via surface-activated peroxides on carbon nanotubes.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.133242]
20. Chaonan Huang, Li Wang, Huiqing Zhang, Weiqiang Tan, Lingxia Wu, ShaSha Wang, Jiping Ma.  (2026)  Cold-Induced Phase Separation Coupled With High-Performance Liquid Chromatography-Fluorescence Detection for Determination of Glyphosate, Aminomethylphosphonic Acid, and Glufosinate in Environmental Water.  JOURNAL OF SEPARATION SCIENCE,  49  (3): (e70399).  [PMID:] [10.1002/jssc.70399]
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