≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature,Argon charged Ships Normal 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.
Product Application：
2-Amino-3-methyl-1-butanol was used in the synthesis of 1-allyl-2-pyrroleimines. It was also used as chiral nucleophile in the total synthesis of benanomicin-pradimicin antibiotics. It was used as homochiral guest compound during synthesis of crown ethers containing two chiral subunits.
| Pubchem Sid | 488185660 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488185660 |
| Sonrisas canónicas | CC(C)C(CO)N |
| IUPAC Name | 2-amino-3-methylbutan-1-ol |
| InChIKey | NWYYWIJOWOLJNR-UHFFFAOYSA-N |
| INCHI | 1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3 |
| Isómeros SMILES | CC(C)C(CO)N |
| WGK Alemania | 3 |
| PubChem CID | 79019 |
| Peso molecular | 103.17 |
| Beilstein | 4(4)1777 |
| Reaxy-Rn | 1209242 |
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 | Organic nitrogen compounds |
| Clase | Organonitrogen compounds |
| Subclass | Amines |
| Intermediate Tree Nodes | Alkanolamines |
| Direct Parent | 1,2-aminoalcohols |
| Alternative Parents | Primary alcohols Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | 1,2-aminoalcohol - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Primary aliphatic amine - Alcohol - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as 1,2-aminoalcohols. These are organic compounds containing an alkyl chain with an amine group bound to the C1 atom and an alcohol group bound to the C2 atom. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 I2215418 | Certificate of Analysis | Jun 15, 2026 | S160983 |
| I2215541 | Certificate of Analysis | Jun 15, 2026 | S160983 |
| I2215542 | Certificate of Analysis | Jun 15, 2026 | S160983 |
| I1721028 | Certificate of Analysis | Apr 09, 2025 | S160983 |
| D23261071 | Certificate of Analysis | Jul 07, 2022 | S160983 |
| Solubilidad | Soluble in water; Soluble in Ether,Ethanol |
|---|---|
| Índice de refracción | 1.45 |
| Punto de inflamación (°F) | 194 °F |
| Punto de inflamación (°C) | 90 °C |
| Punto de ebullición (°C) | 87 °C/11 mmHg |
| Peso molecular | 103.160 g/mol |
| XLogP3 | 0.000 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 103.1 Da |
| Monoisotopic Mass | 103.1 Da |
| Topological Polar Surface Area | 46.300 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 45.300 |
| 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. Chang Ya-Wen, Zhang Jian-Dong, Yang Xiao-Xiao, Li Jing, Gao Li-Li, Huang Shuang-Ping, Guo Xing-Mei, Zhang Cao-Feng, Chang Hong-Hong, Xu Jian-He. (2020) High throughput solid-phase screening of bacteria with cyclic amino alcohol deamination activity for enantioselective synthesis of chiral cyclic β-amino alcohols. BIOTECHNOLOGY LETTERS, 42 (8): (1501-1511). [PMID:32219689] [10.1007/s10529-020-02869-2] |
