≥90% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
Geranylamine is an di-isoprene derivative.Geranylamine may be employed as starting reagent for the total synthesis of a naturally occurring guanidine alkaloid, Nitensidine D. It may be used for the synthesis of 5-alkylamino- and 2,5-bis(alkylamino)-[1,4]-benzoquinone.
| Sorrisi canonici | CC(=CCCC(=CCN)C)C |
|---|---|
| IUPAC Name | (2E)-3,7-dimethylocta-2,6-dien-1-amine |
| InChIKey | AFMZGMJNKXOLEM-JXMROGBWSA-N |
| INCHI | 1S/C10H19N/c1-9(2)5-4-6-10(3)7-8-11/h5,7H,4,6,8,11H2,1-3H3/b10-7+ |
| Isomeri SMILES | CC(=CCC/C(=C/CN)/C)C |
| WGK Germania | 3 |
| Numero UN | 2735 |
| Gruppo di imballaggio | III |
| Peso molecolare | 153.26 |
| Reaxy-Rn | 1757197 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1757197&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 |
| Classe | Prenol lipids |
| Subclass | Monoterpenoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Acyclic monoterpenoids |
| Alternative Parents | Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Acyclic monoterpenoid - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as acyclic monoterpenoids. These are monoterpenes that do not contain a cycle. |
| External Descriptors | Not available |
| Punto di infiammabilità (°F) | 190.4 °F |
|---|---|
| Punto di infiammabilità (°C) | 88 °C |
| Punto di ebollizione (°C) | 105° C (lit.) at 19 mmHg |
| Peso molecolare | 153.260 g/mol |
| XLogP3 | 2.600 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 4 |
| Exact Mass | 153.152 Da |
| Monoisotopic Mass | 153.152 Da |
| Topological Polar Surface Area | 26.000 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 150.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |
| 1. Chenlong Wei, Xinzhu Shan, Yuxuan Huang, Bin Ma, Zhiqiang Zhao, Yian Fang, Chengrui Bai, Zihan Zhang, Peng Zhao, Huijuan Zhang, Yu Hou, Tianjiao Ji, Zhongtang Li, Song Song, Fei Xie, Lei Miao. (2026) FAP-Synergistic Organ-Targeted mRNA-LNP for Overcoming Delivery Barriers in Hepatic and Pulmonary Fibrosis. Journal of the American Chemical Society, [PMID:41731656] [10.1021/jacs.5c16886] |
