1,4-Diiodobenzene - ≥98% , CAS No.624-38-4

CAS: 624-38-4 Cat. No.: D111116 Peso molecular: 329.91 Beilstein Registry Number: 1904546 Número EC: 210-842-2
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
4-IODOPHENYL IODIDE | AM20040890 | Benzene, 1,4-diiodo- | EN300-21234 | InChI=1/C6H4I2/c7-5-1-2-6(8)4-3-5/h1-4 | Benzene,4-diiodo- | DTXSID2022092 | 1,4 di-idobenzene | NSC6297 | NSC-6297 | 1,4 diiodobenzene | 1,4 di-iodobenzene | p-Benzene diiodide | 1,4
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
D111116-5g
8

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
10g
D111116-10g
1

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
25g
D111116-25g
≥10

29,90US$

44,90US$
Guardar 15,00 US$ (33.41%)
100g
D111116-100g
4

81,90US$

122,90US$
Guardar 41,00 US$ (33.36%)
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

Room temperature Ships Normal 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 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

1,4-Diiodobenzene was used in: . total synthesis of martinellic acid, a naturally occurring bradykinin receptor antagonist . preparation of 1,4-bis(p-R-phenylethynyl)benzenes via Pd11/Cu1catalyzed cross-coupling reaction . synthesis of 1,4-diiodo-2,5-didodecylbenzene, starting reagent for the preparation of oligo(1,4-phenylene ethynylene)s . surface-mediated synthesis of epitaxially aligned and separated polyphenylene lines on Cu(110) via Ullmann dehalogenation reaction

Specifications

Sinónimos
4-IODOPHENYL IODIDE | AM20040890 | Benzene, 1, 4-diiodo- | EN300-21234 | InChI=1/C6H4I2/c7-5-1-2-6(8)4-3-5/h1-4 | Benzene, 4-diiodo- | DTXSID2022092 | 1, 4 di-idobenzene | NSC6297 | NSC-6297 | 1, 4 diiodobenzene | 1, 4 di-iodobenzene | p-Benzene diiodide | 1, 4
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504752282
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504752282
Sonrisas canónicasC1=CC(=CC=C1I)I
IUPAC Name1,4-diiodobenzene
InChIKeyLFMWZTSOMGDDJU-UHFFFAOYSA-N
INCHI1S/C6H4I2/c7-5-1-2-6(8)4-3-5/h1-4H
Isómeros SMILES C1=CC(=CC=C1I)I
WGK Alemania 3
Peso molecular 329.91
Beilstein 1904546
Reaxy-Rn 1904546
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1904546&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
ClaseBenzene and substituted derivatives
SubclassHalobenzenes
Intermediate Tree Nodes Not available
Direct ParentIodobenzenes
Alternative Parents Aryl iodides  Organoiodides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Iodobenzene - Aryl iodide - Aryl halide - Hydrocarbon derivative - Organoiodide - Organohalogen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as iodobenzenes. These are aromatic compounds containing one or more iodine atoms attached to a benzene.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

25 results found

Lot NumberCertificate TypeFechaArticulo
H2427474Certificate of AnalysisJun 08, 2026 D111116
F2228236Certificate of AnalysisJan 19, 2026 D111116
K2513667Certificate of AnalysisJun 19, 2025 D111116
K2513223Certificate of AnalysisJun 19, 2025 D111116
K2513221Certificate of AnalysisJun 19, 2025 D111116
K2513220Certificate of AnalysisJun 19, 2025 D111116
F2602095Certificate of AnalysisJun 19, 2025 D111116
D2627085Certificate of AnalysisJun 19, 2025 D111116
F2228229Certificate of AnalysisMar 10, 2025 D111116
E23061048Certificate of AnalysisFeb 07, 2025 D111116
E23061049Certificate of AnalysisFeb 07, 2025 D111116
E23061050Certificate of AnalysisFeb 07, 2025 D111116
C2505770Certificate of AnalysisDec 19, 2024 D111116
B2526246Certificate of AnalysisDec 19, 2024 D111116
B2526247Certificate of AnalysisDec 19, 2024 D111116
B2526248Certificate of AnalysisDec 19, 2024 D111116
H2427471Certificate of AnalysisAug 14, 2024 D111116
H2427473Certificate of AnalysisAug 14, 2024 D111116
H2427476Certificate of AnalysisAug 14, 2024 D111116
F2228241Certificate of AnalysisApr 02, 2024 D111116
C1810030Certificate of AnalysisJul 12, 2023 D111116
H2117139Certificate of AnalysisMay 12, 2023 D111116
H2117136Certificate of AnalysisMay 12, 2023 D111116
A2424033Certificate of AnalysisJun 12, 2022 D111116
E2026134Certificate of AnalysisApr 13, 2022 D111116

Show more ⌵

Propiedades químicas y físicas
SolubilidadSoluble in ether and ethanol. Insoluble in water.
SensibilidadLight sensitive.
Punto de ebullición (°C)285°C
Punto de fusión (°C)128-132°C
Peso molecular329.900 g/mol
XLogP34.100
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count0
Exact Mass329.84 Da
Monoisotopic Mass329.84 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count8
Formal Charge0
Complexity54.900
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
Citations of This Product
Referencias
1. Yudi Feng, Qiangsheng Sun, Jia Guo, Changchun Wang.  (2022)  Design and preparation of glassy molecular precursors by adjusting molecular structures for facile processing of high-performance polymers.  Materials Chemistry Frontiers,  (17): (2511-2523).  [PMID:] [10.1039/D2QM00499B]
2. Xin-Qiao He, Yuan-Yuan Cui, Xiao-Hui Lin, Cheng-Xiong Yang.  (2021)  Fabrication of polyethyleneimine modified magnetic microporous organic network nanosphere for efficient enrichment of non-steroidal anti-inflammatory drugs from wastewater samples prior to HPLC-UV analysis.  TALANTA,      [PMID:34215105] [10.1016/j.talanta.2021.122471]
3. Yuan-Yuan Cui, Huan Yao, Cheng-Xiong Yang, Xiu-Ping Yan.  (2019)  In situ fabrication of microporous organic network coated capillary column for high resolution gas chromatographic separation of hydrocarbons.  ELECTROPHORESIS,      [PMID:30942493] [10.1002/elps.201800540]
4. Li Jingkun, Li Huijuan, Zhao Yanfang, Wang Shanshan, Chen Xiangfeng, Zhao Ru-Song.  (2018)  A hollow microporous organic network as a fiber coating for solid-phase microextraction of short-chain chlorinated hydrocarbons.  MICROCHIMICA ACTA,  185  (9): (1-8).  [PMID:30120575] [10.1007/s00604-018-2955-7]
5. Jianqiang Zhang, Yongsheng Peng, Wenguang Leng, Yanan Gao, Feifei Xu, Jinling Chai.  (2016)  Nitrogen ligands in two-dimensional covalent organic frameworks for metal catalysis.  CHINESE JOURNAL OF CATALYSIS,      [PMID:] [10.1016/S1872-2067(15)61050-6]
6. Wenmin Zhang, Baodi Liao, Shiye Xie, Lan Zhang.  (2024)  Hollow microporous organic network fiber membrane for efficient extraction of okadaic acid from marine organisms.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:39378624] [10.1016/j.chroma.2024.465392]
7. Li Han, Cui Yuanyuan, Zhen Changqing, Lin Xiaohui, Li Ke, Yang Chengxiong.  (2025)  Modification of Microporous Organic Network with Amino Acid for HILIC/RPLC Mixed-Mode High-Performance Liquid Chromatography.  Journal of Analysis and Testing,      [PMID:] [10.1007/s41664-025-00362-1]
8. Ting Wang, Yuan-Yuan Cui, Cheng-Xiong Yang.  (2025)  Fabrication of microporous organic network incorporated monolithic column for improved high performance liquid chromatographic separation of small molecules.  ANALYTICA CHIMICA ACTA,      [PMID:40015778] [10.1016/j.aca.2025.343736]
9. Xin-Qiao He, Yuan-Yuan Cui, Cheng-Xiong Yang.  (2020)  Engineering of amino microporous organic network on zeolitic imidazolate framework-67 derived nitrogen-doped carbon for efficient magnetic extraction of plant growth regulators.  TALANTA,      [PMID:33379085] [10.1016/j.talanta.2020.121876]
10. Li Chen, Tao Yu, Le Huang, Qiaomei Lu, Wenmin Zhang, Lan Zhang.  (2025)  Effective extraction of trace cytokinins in plants based on a carboxyl functionalized microporous organic network.  Analytical Methods,      [PMID:40197978] [10.1039/D5AY00123D]
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.