≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged Ships FedEx DG Service 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Tetrahydrofurfurylamine was used to study specific interactions between unlike molecules by calculating the molar excess enthalpies. It can be used to produce N-tetrahydrofurfuryl-phthalimide with phthalic acid anhydride by heating.
| Pubchem Sid | 504758136 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504758136 |
| Canonical Smiles | C1CC(OC1)CN |
| IUPAC Name | oxolan-2-ylmethanamine |
| InChIKey | YNOGYQAEJGADFJ-UHFFFAOYSA-N |
| INCHI | 1S/C5H11NO/c6-4-5-2-1-3-7-5/h5H,1-4,6H2 |
| Isomeric SMILES | C1CC(OC1)CN |
| WGK Germany | 3 |
| RTECS | LV0175000 |
| PubChem CID | 253298 |
| UN Number | 2943 |
| Packing Group | III |
| Molecular Weight | 101.15 |
| Beilstein | 102729 |
| Reaxy-Rn | 102729 |
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 | Organoheterocyclic compounds |
| Class | Tetrahydrofurans |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tetrahydrofurans |
| Alternative Parents | Oxacyclic compounds Dialkyl ethers Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Tetrahydrofuran - Oxacycle - Ether - Dialkyl ether - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen. |
| 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 |
|---|---|---|---|
 C2605593 | Certificate of Analysis | Feb 03, 2026 | T111157 |
| C2605594 | Certificate of Analysis | Feb 03, 2026 | T111157 |
| D2509091 | Certificate of Analysis | Aug 13, 2024 | T111157 |
| I2424576 | Certificate of Analysis | Aug 13, 2024 | T111157 |
| I2424577 | Certificate of Analysis | Aug 13, 2024 | T111157 |
| C2416027 | Certificate of Analysis | Mar 08, 2024 | T111157 |
| C2416033 | Certificate of Analysis | Mar 08, 2024 | T111157 |
| J2327710 | Certificate of Analysis | Oct 19, 2023 | T111157 |
| J2327711 | Certificate of Analysis | Oct 19, 2023 | T111157 |
| J2327718 | Certificate of Analysis | Oct 19, 2023 | T111157 |
| J2327719 | Certificate of Analysis | Oct 19, 2023 | T111157 |
| G23131350 | Certificate of Analysis | Jun 09, 2023 | T111157 |
| G23131351 | Certificate of Analysis | Jun 09, 2023 | T111157 |
| Sensitivity | Air and Moisture sensitive |
|---|---|
| Refractive Index | 1.454 |
| Flash Point(°F) | 109.4 °F |
| Flash Point(°C) | 45℃ |
| Boil Point(°C) | 153～154°C |
| Molecular Weight | 101.150 g/mol |
| XLogP3 | -0.300 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 101.084 Da |
| Monoisotopic Mass | 101.084 Da |
| Topological Polar Surface Area | 35.300 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 56.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Shuxing Zhang, Jiali Zheng, Zhihui Li, Xiaoshu Ding, Yanji Wang. (2023) A green catalytic reaction system for the synthesis 5-amino-1-pentanol with furfural and ionic liquid hydroxylamine salt as the initial raw material. Molecular Catalysis, [PMID:] [10.1016/j.mcat.2023.112995] |
| 2. Tao Shen, Zhenwen Hu, Qingya Liu, Tingyu Lei, Zhenyu Liu. (2021) A method to evaluate hydrogen donation ability of hydrogen-storage solvent in hydrogenation process by radical-precursor compounds. FUEL, [PMID:] [10.1016/j.fuel.2021.122741] |
| 3. Shuxing Zhang, Xiaoshu Ding, Yanji Wang. (2025) The Effect of Preparation Conditions on the Performance of Hydrogenolysis of Furfurylamine to 5-Amino-1-Pentanol over Pt/ZrO2 Catalyst. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, [PMID:] [10.1021/acs.iecr.4c04908] |
| 4. Chenglong Dong, Hongtao Wang, Haochen Du, Jiebang Peng, Yang Cai, Shuai Guo, Jianli Zhang, Chanatip Samart, Mingyue Ding. (2019) Ru/HZSM-5 as an efficient and recyclable catalyst for reductive amination of furfural to furfurylamine. Molecular Catalysis, [PMID:] [10.1016/j.mcat.2019.110755] |
