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4-Iodoaniline - 98%, high purity , CAS No.540-37-4

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4-Iodoaniline - 98%, high purity , CAS No.540-37-4

9 Citations

COA

Grade & Purity:

≥98%

Cas Number: 540-37-4
Molecular Weight: 219.02
Beilstein Registry Number: 774101
EC Number: 208-743-4
MDL number: MFCD00007848
PubChem CID: 10893
PubChem SID: 504752022

In stock

Item Number

I107029

Grouped product items
SKU	Size	Availability	Price
I107029-5g	5g	5	$9.90
I107029-10g	10g	1	$14.90
I107029-25g	25g	≥10	$27.90
I107029-50g	50g	2	$49.90
I107029-100g	100g	4	$89.90
I107029-250g	250g	1	$199.90
I107029-500g	500g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$358.90

View related series

Amine (194) Amines_C6 (2) Nitrogenous compounds (2445) Non heterocyclic block (8163)

Basic Description

Synonyms	p-Aminophenyl iodide \| 4-iodophenylamine \| 4-Iodo-phenylamine \| para-amino-iodo-benzene \| 4-Iodobenzenamine \| 4-iodo-benzenamine \| Aniline, p-iodo- \| Benzenamine, 4-iodo- \| CCRIS 9122 \| 0BMK56397B \| NSC9246 \| NSC-9246 \| p-Iodoaniline \| p-iodo-aniline \| 4-
Specifications & Purity	≥98%
Storage Temp	Store at 2-8°C,Protected from light,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	4-Iodoaniline is the most potent methaemoglobin former.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Aniline and substituted anilines

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Aniline and substituted anilines
Intermediate Tree Nodes	Not available
Direct Parent	Aniline and substituted anilines
Alternative Parents	Iodobenzenes Aryl iodides Primary amines Organopnictogen compounds Organoiodides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Aniline or substituted anilines - Iodobenzene - Halobenzene - Aryl iodide - Aryl halide - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organoiodide - Organohalogen compound - Amine - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504752022
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504752022
IUPAC Name	4-iodoaniline
INCHI	InChI=1S/C6H6IN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2
InChIKey	VLVCDUSVTXIWGW-UHFFFAOYSA-N
Smiles	C1=CC(=CC=C1N)I
Isomeric SMILES	C1=CC(=CC=C1N)I
WGK Germany	3
RTECS	BY3850000
Molecular Weight	219.02
Beilstein	774101
Reaxy-Rn	774101
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=774101&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

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.

26 results found

Lot Number	Certificate Type	Date	Item
H2302820	Certificate of Analysis	May 09, 2025	I107029
E23231072	Certificate of Analysis	Feb 07, 2025	I107029
E23231070	Certificate of Analysis	Feb 07, 2025	I107029
E23231069	Certificate of Analysis	Feb 07, 2025	I107029
E2323826	Certificate of Analysis	Feb 07, 2025	I107029
E23231065	Certificate of Analysis	Feb 07, 2025	I107029
E23231067	Certificate of Analysis	Feb 07, 2025	I107029
E23231061	Certificate of Analysis	Feb 07, 2025	I107029
E23231073	Certificate of Analysis	Feb 07, 2025	I107029
K2203228	Certificate of Analysis	Aug 22, 2024	I107029
I2411020	Certificate of Analysis	Mar 27, 2024	I107029
D2424266	Certificate of Analysis	Mar 27, 2024	I107029
D2424267	Certificate of Analysis	Mar 27, 2024	I107029
D2424269	Certificate of Analysis	Mar 27, 2024	I107029
D2424270	Certificate of Analysis	Mar 27, 2024	I107029
D2407354	Certificate of Analysis	Mar 11, 2024	I107029
D2407355	Certificate of Analysis	Mar 11, 2024	I107029
L2121133	Certificate of Analysis	Sep 21, 2023	I107029
L2121127	Certificate of Analysis	Sep 21, 2023	I107029
L2121136	Certificate of Analysis	Sep 21, 2023	I107029
L2121128	Certificate of Analysis	Sep 21, 2023	I107029
H2302804	Certificate of Analysis	Aug 09, 2023	I107029
D2116386	Certificate of Analysis	Apr 11, 2023	I107029
F2124079	Certificate of Analysis	Mar 16, 2023	I107029
G1916076	Certificate of Analysis	Feb 03, 2023	I107029
E23231064	Certificate of Analysis	Jan 06, 2023	I107029

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Chemical and Physical Properties

Solubility	Slightly soluble in water.Soluble in chloroform, methanol,diethyl ether,alcohol
Sensitivity	Light and air sensitive
Melt Point(°C)	61-63°C
Molecular Weight	219.020 g/mol
XLogP3	2.300
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	0
Exact Mass	218.954 Da
Monoisotopic Mass	218.954 Da
Topological Polar Surface Area	26.000 Å²
Heavy Atom Count	8
Formal Charge	0
Complexity	66.900
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Xiaohong Liu, Xuan Song, Bifang Chen, Jiaming Liu, Zhiqiang Feng, Wenchao Zhang, Juanjuan Zeng, Liyan Liang. (2022) Self-healing and shape-memory epoxy thermosets based on dynamic diselenide bonds. REACTIVE & FUNCTIONAL POLYMERS, 170 (105121).
2. Kui Wu, Yajun Li. (2019) Solubility Measurement and Phase Equilibrium Modeling of 2-Aminobenzamide in 15 Pure Solvents. JOURNAL OF CHEMICAL AND ENGINEERING DATA, 64 (9): (3951–3959).
3. Gailan Guo, Libin Liu, Qiang Zhang, Chenguang Pan, Qiqi Zou. (2018) Solution-processable, durable, scalable, fluorine-grafted graphene-based superhydrophobic coating for highly efficient oil/water separation under harsh environment. NEW JOURNAL OF CHEMISTRY, 42 (5): (3819-3827).
4. Yunji Xie, Bei Liu, Zheng Chen, Xiaocui Han, Baijun Liu, Haibo Zhang, Jinhui Pang, Zhenhua Jiang. (2017) Graft fluorinated poly(arylene ether ketone)s containing highly dense sulfonic-acid-functionalized pendants for proton exchange membranes by C–N coupling. POLYMER, 131 (84).
5. Meng Ruan, Qiqin Wang, Huihui Wu, Yuqiang Wang, Hai Han, Zhengjin Jiang. (2017) Preparation and evaluation of tert-leucine derivative functionalized polymeric monoliths for micro-liquid chromatography. ELECTROPHORESIS, 38 (22-23): (3020-3028).
6. Bei Liu, Zheng Chen, Liming Lin, Yuntao Han, Jinhui Pang, Zhenhua Jiang. (2016) Synthesis and characterization of poly(arylene ether ketone)s with 3,6-diphenyl-9H-carbazole pendants using C–N coupling reaction. HIGH PERFORMANCE POLYMERS,
7. Wang Minchao, Jamal Ruxangul, Wang Yujie, Yang Lei, Liu Fangfang, Abdiryim Tursun. (2015) Functionalization of Graphene Oxide and its Composite with Poly(3,4-ethylenedioxythiophene) as Electrode Material for Supercapacitors. Nanoscale Research Letters, 10 (1): (1-11).
8. Ting Li, Yunqiao Ding, Libin Liu, Jian Liu, Wenyuan Fang, Yu Xiang, Tianduo Li. (2015) Facile fabrication of multifunctional perfluoroalkyl functionalized graphene hydrogel via a synchronous reduction and grafting strategy. Journal of Materials Chemistry A, 3 (43): (21744-21753).
9. He Meng, Li Rui, Cheng Chuanqi, Liu Cuibo, Zhang Bin. (2024) Microenvironment regulation breaks the Faradaic efficiency-current density trade-off for electrocatalytic deuteration using D2O. Nature Communications, 15 (1): (1-10).

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