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Iodoform - 99%, high purity , CAS No.75-47-8

    Grade & Purity:
  • AR
  • ≥99%
In stock
Item Number
I108194
Grouped product items
SKU Size
Availability
Price Qty
I108194-5g
5g
5
$39.90
I108194-25g
25g
8
$68.90
I108194-50g
50g
4
$104.90
I108194-100g
100g
1
$194.90
I108194-250g
250g
2
$388.90
I108194-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$682.90
View related series
Halogenated hydrocarbon (21)

Basic Description

Synonyms IODOFORM (USP MONOGRAPH) | methyl triiodide | IODOFORM | Methane, triiodo- | NCI-C04568 | CAS-75-47-8 | NCGC00256394-01 | Trijodmethane [Czech] | NSC 26251 | IODOFORMUM [HPUS] | Iodoformum | Jodoform | s12111 | UNII-KXI2J76489 | IODOFORM [MI] | HSDB 4099
Specifications & Purity AR, ≥99%
Storage Temp Protected from light
Shipped In Normal
Grade AR

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organohalogen compounds
Class Alkyl halides
Subclass Halomethanes
Intermediate Tree Nodes Not available
Direct Parent Trihalomethanes
Alternative Parents Organoiodides  Hydrocarbon derivatives  Alkyl iodides  
Molecular Framework Aliphatic acyclic compounds
Substituents Trihalomethane - Hydrocarbon derivative - Organoiodide - Alkyl iodide - Aliphatic acyclic compound
Description This compound belongs to the class of organic compounds known as trihalomethanes. These are organic compounds in which exactly three of the four hydrogen atoms of methane (CH4) are replaced by halogen atoms.
External Descriptors one-carbon compound - iodomethanes

Associated Targets(Human)

VDR Tclin Vitamin D receptor (26531 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
pfk 6-phospho-1-fructokinase (7870 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ddn Putative uncharacterized protein (49 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488180058
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488180058
IUPAC Name iodoform
INCHI InChI=1S/CHI3/c2-1(3)4/h1H
InChIKey OKJPEAGHQZHRQV-UHFFFAOYSA-N
Smiles C(I)(I)I
Isomeric SMILES C(I)(I)I
WGK Germany 3
RTECS PB7000000
Molecular Weight 393.73
Beilstein 1697010
Reaxy-Rn 1697010
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1697010&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.

17 results found

Lot Number Certificate Type Date Item
D23081211 Certificate of Analysis Jan 08, 2025 I108194
D23081199 Certificate of Analysis Jan 08, 2025 I108194
D23081200 Certificate of Analysis Jan 08, 2025 I108194
D23081207 Certificate of Analysis Jan 08, 2025 I108194
D23081208 Certificate of Analysis Jan 08, 2025 I108194
D23081203 Certificate of Analysis Jan 08, 2025 I108194
D23081206 Certificate of Analysis Jan 08, 2025 I108194
H2217450 Certificate of Analysis May 07, 2024 I108194
H2217447 Certificate of Analysis May 07, 2024 I108194
H2217449 Certificate of Analysis May 07, 2024 I108194
H2217448 Certificate of Analysis May 07, 2024 I108194
D23081198 Certificate of Analysis Mar 06, 2023 I108194
D23081202 Certificate of Analysis Mar 06, 2023 I108194
H2217451 Certificate of Analysis Jun 13, 2022 I108194
H2217452 Certificate of Analysis Jun 13, 2022 I108194
A2416061 Certificate of Analysis Jun 13, 2022 I108194
C2025134 Certificate of Analysis Jan 19, 2022 I108194

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Chemical and Physical Properties

Solubility Soluble in water, ether, acetic acid, ethanol, chloroform, ether, glycerol, carbon disulfide, olive oil, benzene and acetone. Slightly soluble in petroleum ether.
Sensitivity Light sensitive.
Melt Point(°C) 118-123℃
Molecular Weight 393.732 g/mol
XLogP3 2.700
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 0
Rotatable Bond Count 0
Exact Mass 393.721 Da
Monoisotopic Mass 393.721 Da
Topological Polar Surface Area 0.000 Ų
Heavy Atom Count 4
Formal Charge 0
Complexity 8.000
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

1. Menglin Wu, Shunke Ding, Zhongqi Cao, Zhenqi Du, Yuyang Tang, Xiaoyan Chen, Wenhai Chu.  (2022)  Insights into the formation and mitigation of iodinated disinfection by-products during household cooking with Laminaria japonica (Haidai).  WATER RESEARCH,  225  (119177). 
2. Rui Wang, Duoduo Lu, Hui Wang, Haoyu Zou, Ting Bai, Chulei Feng, Quankui Lin.  (2021)  “Kill-release” antibacterial polysaccharides multilayer coating based therapeutic contact lens for effective bacterial keratitis treatment.  RSC Advances,  11  (42): (26160-26167). 
3. Xia Zhao, Sihao Liu, Yuemei Han, Yuqin Wang, Quankui Lin.  (2021)  Preparation of 5-fluorouracil loaded chitosan microtube via in situ precipitation for glaucoma drainage device application: in vitro and in vivo investigation.  JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION,  32  (14): (1849-1864). 
4. Feng Feng, Jiamei Liu, Mingxing Zhao, Lu Yu, Haixin Wang, Chunshan Lu, Qunfeng Zhang, Jia Zhao, Yanxia Sun, Jie Cen, Xiaonian Li.  (2021)  Study of an Environmentally Friendly Method for the Dissolution of Precious Metal with Ionic Liquid and Iodoalkane.  Metals,  11  (6): (919). 
5. Chao Fang, Xingyu Wang, Rong Xiao, Shunke Ding, Baiyang Chen, Wenhai Chu.  (2021)  Rejection of chlorinated, brominated, and iodinated trihalomethanes by multi-stage reverse osmosis: Efficiency and mechanisms.  CHEMOSPHERE,  268  (129307). 
6. Hengxuan Zhao, Yuefei Ji, Deyang Kong, Junhe Lu, Xiaoming Yin, Quansuo Zhou.  (2019)  Degradation of iohexol by Co2+ activated peroxymonosulfate oxidation: Kinetics, reaction pathways, and formation of iodinated byproducts.  CHEMICAL ENGINEERING JOURNAL,  373  (1348). 
7. Qian Tang, Zhichao Hu, Haiming Jin, Gang Zheng, XingFang Yu, Gang Wu, Haixiao Liu, Zhenzhong Zhu, Huazi Xu, Changqing Zhang, Liyan Shen.  (2019)  Microporous polysaccharide multilayer coated BCP composite scaffolds with immobilised calcitriol promote osteoporotic bone regeneration both in vitro and in vivo.  Theranostics,  (4): ( 1125–1143). 
8. Chujuan Huang, Nobuko Yamashita, Amorn Chaiyasat, Xiang Liu, Masayoshi Okubo.  (2018)  Microsuspension iodine transfer polymerization (ms ITP) for synthesis of micrometer-size, “hydrophilic” polymer particles.  POLYMER,  154  (128). 
9. Huanlong Liu, Yufeng Tang, Wei Zhao, Wei Ding, Jijian Xu, Chenliang Liang, Zhichao Zhang, Tianquan Lin, Fuqiang Huang.  (2018)  Facile Synthesis of Nitrogen and Halogen Dual-Doped Porous Graphene as an Advanced Performance Anode for Lithium-Ion Batteries.  Advanced Materials Interfaces,  (5): (1701261). 
10. Yanli Liu, Jiazhu Xu, Yan Zhou, Zhaoyang Ye, Wen-Song Tan.  (2017)  Layer-by-layer assembled polyelectrolytes on honeycomb-like porous poly(ε-caprolactone) films modulate the spatial distribution of mesenchymal stem cells.  Materials Science & Engineering C-Materials for Biological Applications,  78  (579). 
11. Jun Wang, Haiyang Liu, Fei Leng, Linling Zheng, Jinghua Yang, Wei Wang, Cheng Zhi Huang.  (2014)  Autofluorescent and pH-responsive mesoporous silica for cancer-targeted and controlled drug release.  MICROPOROUS AND MESOPOROUS MATERIALS,  186  (187). 
12. Yan Wang, Song Wang, Zhiyan Sui, Yiman Gu, Yanchao Zhang, Jian Gao, Yijia Lei, Jialin Zhao, Na Li, JingYi Wu, Zhe Wang.  (2024)  “Fishbone” Design of Amino/N-Spirocyclic Cations toward High-Performance Poly(triphenylene piperidine) Anion-Exchange Membranes for Fuel Cells.  ACS Applied Materials & Interfaces,  16  (3): (4003-4012). 
13. Hao Huang, Zexin Liu, Hanxin Jian, Yuan Yao, Bing Xue, Shuguang Yang.  (2024)  Humidity-Adaptive Behaviors of Alginate/Chitosan Complex Fiber.  ACS Applied Polymer Materials,  (8): (4634-4641). 
14. Shuang Chen, Yue Qiao, Youwei Jiang, Wei Qiu, Shuang Zang, Jing Zhang, Xianshi Wang, Jun Ma.  (2024)  Trace analysis of 59 halogenated aromatic disinfection byproducts through the SPE-LC-MS/MS method and their occurrence and transformation during chlorine disinfection.  Journal of Environmental Sciences,     

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