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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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A111256-5g
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5g |
4
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$9.90
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A111256-25g
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25g |
3
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$30.90
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A111256-100g
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100g |
4
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$82.90
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A111256-500g
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500g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
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$216.90
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| Synonyms | 2-Imino-4-thiobiuret, 99% | Amidinothiourea | EN300-34314 | guanyl isothiourea | (diaminomethylidene)thiourea | 1-(diaminomethylene)thiourea | EINECS 218-308-0 | E75731 | BBL008942 | diaminomethylidenethiourea | N-Amidinothiourea | N-amidino-thiourea | 1- |
|---|---|
| Specifications & Purity | ≥98% |
| Shipped In | Normal |
| Product Description |
Application 2-Imino-4-thiobiuret is used in the design and synthesis of guanylthiourea derivatives which are potential inhibitors of plasmodium falciparum dihydrofolate reductase enzyme. 2-Imino-4-thiobiuret is also used as a reagent in recyclization reactions of N-arylmaleimides with polynucleophilic compounds. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic nitrogen compounds |
| Class | Organonitrogen compounds |
| Subclass | Guanidines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Guanidines |
| Alternative Parents | Propargyl-type 1,3-dipolar organic compounds Carboximidamides Organosulfur compounds Organopnictogen compounds Imines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Guanidine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organopnictogen compound - Hydrocarbon derivative - Organosulfur compound - Imine - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as guanidines. These are compounds containing a guanidine moiety, with the general structure (R1R2N)(R3R4N)C=N-R5. |
| External Descriptors | Not available |
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| Pubchem Sid | 488192282 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488192282 |
| IUPAC Name | diaminomethylidenethiourea |
| INCHI | InChI=1S/C2H6N4S/c3-1(4)6-2(5)7/h(H6,3,4,5,6,7) |
| InChIKey | OKGXJRGLYVRVNE-UHFFFAOYSA-N |
| Smiles | C(=NC(=S)N)(N)N |
| Isomeric SMILES | C(=NC(=S)N)(N)N |
| WGK Germany | 3 |
| RTECS | YR8250000 |
| Molecular Weight | 118.16 |
| Reaxy-Rn | 3587727 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3587727&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 | Mar 04, 2025 | A111256 | |
| Certificate of Analysis | Mar 04, 2025 | A111256 | |
| Certificate of Analysis | Jun 20, 2024 | A111256 | |
| Certificate of Analysis | Jun 20, 2024 | A111256 | |
| Certificate of Analysis | May 07, 2022 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 | |
| Certificate of Analysis | Dec 13, 2021 | A111256 |
| Solubility | Soluble in water (70g/L). |
|---|---|
| Melt Point(°C) | 160-164°C |
| Molecular Weight | 118.160 g/mol |
| XLogP3 | -1.300 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 118.031 Da |
| Monoisotopic Mass | 118.031 Da |
| Topological Polar Surface Area | 123.000 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 102.000 |
| 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. Lulu Zhang, Long Jiang, Yaojie Liu, Zongjiang Yu, Ximin Chen, Xiaomeng Su, Mo Xian, Weizhi Sun, Chao Xu. (2023) The design and adsorption behaviors study of Pd(II) removal materials deriving from quantitative electron transfer ratio evaluation. Journal of Environmental Chemical Engineering, 11 (110264). |
| 2. Zhu Lingkai, Xi Man, Yao Yuyuan, Lan Ping. (2023) Thiol -functionalized activated carbon fibers as efficient adsorbents for Pb2+. MATERIALS CHEMISTRY AND PHYSICS, 302 (127552). |
| 3. Xiao Xudong, Lin Siying, Zhang Liping, Meng Huiyuan, Zhou Jing, Li Qi, Liu Jianan, Qiao Panzhe, Jiang Baojiang, Fu Honggang. (2022) Constructing Pd-N interactions in Pd/g-C3N4 to improve the charge dynamics for efficient photocatalytic hydrogen evolution. Nano Research, 15 (4): (2928-2934). |
| 4. Heping Wang, Bang Feng, Qianwen Zhang, Qiang Du, Qiuhong Bai, Cong Li, Yehua Shen. (2021) Amidinothiourea-linked covalent organic framework for the adsorption of heavy metal ions. POLYMER INTERNATIONAL, 71 (1): (38-46). |
| 5. Fangxiang Song, Xianquan Ao, Qianlin Chen. (2022) Effect of heteroatom doping on the charge storage and operating voltage window of nickel-based sulfide composite electrodes in alkaline electrolytes. CHEMICAL ENGINEERING JOURNAL, 427 (130885). |
| 6. Chaokun Yang, Yanglin Chen, Ping Xu, Li Yang, Jiaxu Zhang, Jianmin Sun. (2020) Facile synthesis of zinc halide-based ionic liquid for efficient conversion of carbon dioxide to cyclic carbonates. Molecular Catalysis, 480 (110637). |
| 7. Huicai Wang, Zhenwen Wang, Ruirui Yue, Feng Gao, Ruili Ren, Junfu Wei, Xiaolei Wang, Zhiyun Kong. (2020) Functional group-rich hyperbranched magnetic material for simultaneous efficient removal of heavy metal ions from aqueous solution. JOURNAL OF HAZARDOUS MATERIALS, 384 (121288). |
| 8. Lei Guo, Lei Zhu, Savaş Kaya, Rui Sun, Alessandra Gilda Ritacca, Kai Wang, Jun Chang. (2024) Electrochemical and surface investigations of N, S codoped carbon dots as effective corrosion inhibitor for mild steel in acidic solution. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 702 (135062). |