≥98% 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 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
DL-Alaninol has been used in the synthesis of:
· N6-α-(I-hydroxypropyl) lysine
· diastereomers of DL-β-amino alcohols
· enantiopure and racemic samples of 2-methyl-N-tosylaziridine
· (±)-3-(5-dimethylcarbamoyl-pent-1-enyl)-N-(2-hydroxy-1-methyl-ethyl)benzamide
| Pubchem Sid | 488179878 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488179878 |
| Sourires canoniques | CC(CO)N |
| IUPAC Name | 2-aminopropan-1-ol |
| InChIKey | BKMMTJMQCTUHRP-UHFFFAOYSA-N |
| INCHI | 1S/C3H9NO/c1-3(4)2-5/h3,5H,2,4H2,1H3 |
| Isomères SMILES | CC(CO)N |
| WGK Allemagne | 3 |
| Numéro ONU | 2735 |
| Groupe d'emballage | I |
| Poids moléculaire | 75.11 |
| Beilstein | 1209234 |
| Reaxy-Rn | 1209234 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209234&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 | Organic nitrogen compounds |
| Classe | 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 |
| Description | 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 | a small molecule |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
 E2227129 | Certificate of Analysis | Mar 11, 2026 | A117165 |
| E2227231 | Certificate of Analysis | Mar 11, 2026 | A117165 |
| E2227232 | Certificate of Analysis | Mar 11, 2026 | A117165 |
| E2227237 | Certificate of Analysis | Mar 11, 2026 | A117165 |
| E2227240 | Certificate of Analysis | Mar 11, 2026 | A117165 |
| L2102393 | Certificate of Analysis | Sep 09, 2025 | A117165 |
| L2102394 | Certificate of Analysis | Sep 09, 2025 | A117165 |
| K2117507 | Certificate of Analysis | Sep 04, 2025 | A117165 |
| A2107149 | Certificate of Analysis | Oct 09, 2024 | A117165 |
| J2429296 | Certificate of Analysis | Jul 03, 2024 | A117165 |
| B2328310 | Certificate of Analysis | May 05, 2022 | A117165 |
| B2328313 | Certificate of Analysis | May 05, 2022 | A117165 |
| I2318182 | Certificate of Analysis | May 05, 2022 | A117165 |
| Solubilité | Fully miscible in water. |
|---|---|
| Sensibilité | Moisture & air sensitive |
| Indice de réfraction | 1.448-1.451 |
| Rotation spécifique [α] | [α]/D +1.0 to −1.0° |
| Point d'éclair (°F) | 183.2 °F |
| Point d'éclair (°C) | 83°C |
| Point d'ébullition (°C) | 173-176°C |
| Point de fusion (°C) | 8°C |
| Poids moléculaire | 75.110 g/mol |
| XLogP3 | -1.000 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 75.0684 Da |
| Monoisotopic Mass | 75.0684 Da |
| Topological Polar Surface Area | 46.300 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 22.900 |
| 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. Xiangzhan Meng, Yongqiang Zhang, Zengxi Li, Hui Wang, Suojiang Zhang. (2019) Selective Oxidation of Amino Alcohols to Amino Acids over Au Supported on Monoclinic ZrO2: Dominant Active Sites and Kinetic Study. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, [PMID:] [10.1021/acs.iecr.9b00442] |
| 2. Sen Liu, Hongxia Gao, Chuan He, Zhiwu Liang. (2018) Experimental evaluation of highly efficient primary and secondary amines with lower energy by a novel method for post-combustion CO2 capture. APPLIED ENERGY, [PMID:] [10.1016/j.apenergy.2018.10.031] |
| 3. Yan Ouyang, Qi Liu, Tong Luo, Qinlan Luo, Min Xiao, Hongxia Gao, Zhiwu Liang. (2024) Experimental and computational study of the thermal degradation of primary amines used in CO2 capture. CHEMICAL ENGINEERING SCIENCE, [PMID:] [10.1016/j.ces.2024.119786] |
| 4. Min Zhou, Ningbo Yu, Qiang Sun, Hongxia Gao, Jinhang Fan, Zhiwu Liang. (2025) Combined experimental and computational study on elucidating steric effects in amine-based CO2 capture. CHEMICAL ENGINEERING SCIENCE, [PMID:] [10.1016/j.ces.2025.122015] |
| 5. Qi Liu, Yan Ouyang, Tong Luo, Qinlan Luo, Min Xiao, Hongxia Gao, Zhiwu Liang. (2025) Thermal degradation of primary amines blended with N,N-dimethylethanolamine in post-combustion carbon capture. AICHE JOURNAL, [PMID:] [10.1002/aic.70178] |
| 6. Ningbo Yu, Shaofei Wang, Min Zhou, Min Xiao, Bo Jin, Hongxia Gao, Zhiwu Liang. (2026) Unveiling solvent encapsulation-driven kinetic inversion in CO2 absorption by water-lean amine solvents. AICHE JOURNAL, [PMID:] [10.1002/aic.70260] |
