Determine the necessary mass, volume, or concentration for preparing a solution.
This is a demo store. No orders will be fulfilled.
| 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
|
|
| 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 |
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 |
|
|
|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| 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= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jan 08, 2025 | I108194 | |
| Certificate of Analysis | Jan 08, 2025 | I108194 | |
| Certificate of Analysis | Jan 08, 2025 | I108194 | |
| Certificate of Analysis | Jan 08, 2025 | I108194 | |
| Certificate of Analysis | Jan 08, 2025 | I108194 | |
| Certificate of Analysis | Jan 08, 2025 | I108194 | |
| Certificate of Analysis | Jan 08, 2025 | I108194 | |
| Certificate of Analysis | May 07, 2024 | I108194 | |
| Certificate of Analysis | May 07, 2024 | I108194 | |
| Certificate of Analysis | May 07, 2024 | I108194 | |
| Certificate of Analysis | May 07, 2024 | I108194 | |
| Certificate of Analysis | Mar 06, 2023 | I108194 | |
| Certificate of Analysis | Mar 06, 2023 | I108194 | |
| Certificate of Analysis | Jun 13, 2022 | I108194 | |
| Certificate of Analysis | Jun 13, 2022 | I108194 | |
| Certificate of Analysis | Jun 13, 2022 | I108194 | |
| Certificate of Analysis | Jan 19, 2022 | I108194 |
| 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 |
| 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, 9 (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 (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, 6 (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, |