Determine the necessary mass, volume, or concentration for preparing a solution.
≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Dimethylallyl Pyrophosphate (triammonium salt) undergoes condensation along with isopentyl pyrophosphate to yield geranyl pyrophosphate. Dimethylallyl Pyrophosphate (triammonium salt) further undergoes condensation with a second isopentyl pyrophosphate, yielding farnesyl pyrophosphate. The process of farnesylation is essential for a function of a number of proteins involved in signal transduction.
| Canonical Smiles | CC(=C)CCOP(=O)([O-])OP(=O)([O-])[O-].[NH4+].[NH4+].[NH4+] |
|---|---|
| IUPAC Name | triazanium;[3-methylbut-3-enoxy(oxido)phosphoryl] phosphate |
| InChIKey | JREYOWJEWZVAOR-UHFFFAOYSA-N |
| INCHI | 1S/C5H12O7P2.3H3N/c1-5(2)3-4-11-14(9,10)12-13(6,7)8;;;/h1,3-4H2,2H3,(H,9,10)(H2,6,7,8);3*1H3 |
| Isomeric SMILES | CC(=C)CCOP(=O)([O-])OP(=O)([O-])[O-].[NH4+].[NH4+].[NH4+] |
| Alternate CAS | 358-72-5 |
| Molecular Weight | 297.18 |
| Reaxy-Rn | 45065528 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=45065528&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Prenol lipids |
| Subclass | Isoprenoid phosphates |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Isoprenoid phosphates |
| Alternative Parents | Organic pyrophosphates Alkyl phosphates Quaternary ammonium salts Organooxygen compounds Organic salts Organic oxides Hydrocarbon derivatives Amines Organic cations |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Organic pyrophosphate - Isoprenoid phosphate - Alkyl phosphate - Phosphoric acid ester - Organic phosphoric acid derivative - Quaternary ammonium salt - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Amine - Organic cation - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as isoprenoid phosphates. These are prenol lipids containing a phosphate group linked to an isoprene (2-methylbuta-1,3-diene) unit. |
| External Descriptors | Not available |
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 | Dec 13, 2025 | D353736 | |
| Certificate of Analysis | Dec 13, 2025 | D353736 | |
| Certificate of Analysis | Jul 09, 2025 | D353736 | |
| Certificate of Analysis | Jul 09, 2025 | D353736 | |
| Certificate of Analysis | Nov 06, 2024 | D353736 | |
| Certificate of Analysis | Aug 17, 2024 | D353736 | |
| Certificate of Analysis | Aug 17, 2024 | D353736 | |
| Certificate of Analysis | Apr 17, 2024 | D353736 | |
| Certificate of Analysis | Apr 17, 2024 | D353736 | |
| Certificate of Analysis | May 12, 2023 | D353736 | |
| Certificate of Analysis | May 12, 2023 | D353736 | |
| Certificate of Analysis | May 12, 2023 | D353736 | |
| Certificate of Analysis | May 12, 2023 | D353736 |
| Molecular Weight | 297.180 g/mol |
|---|---|
| XLogP3 | |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 5 |
| Exact Mass | 297.085 Da |
| Monoisotopic Mass | 297.085 Da |
| Topological Polar Surface Area | 125.000 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 273.000 |
| 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 | 4 |
| 1. Baodong Hu, Jingwen Zhou, Jianghua Li, Jian Chen, Guocheng Du, Fang Zhong, Yucheng Zhao, Xinrui Zhao. (2025) Efficient Biosynthesis of Furanocoumarin Intermediate Marmesin by Engineered Escherichia coli. ACS Synthetic Biology, [PMID:40014795] [10.1021/acssynbio.4c00892] |
| 2. Zili Yang, Xin Chen, Liru Zheng, Qinping Hu, Mengwei Bu, Jiang Duan, Aidong Zhang. (2025) Design and synthesis of aminol- and phenylamide-containing phosphonic acids and their biological activity evaluation. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, [PMID:41162073] [10.1016/j.pestbp.2025.106690] |