(±)-2-Amino-1-butanol - ≥97% , CAS No.96-20-8

CAS: 96-20-8 Cat. No.: A106025 Peso molecular: 89.14 Beilstein Registry Number: 4(4)1705 Número EC: 202-488-2
Disponible para pedir
GRADE & PURITY ≥97%
Synonyms
2-Amino-butan-1-ol | 2-Aminobutan-1-ol | 2-Amino-1-butanol, 97% | 1-(r,s)-(hydroxymethyl)propylamine | (?)-2-Amino-1-butanol | SB83767 | (+)-2-Amino-1-butanol | [(1R)-1-(hydroxymethyl)propyl]ammonium | SY049464 | (+/-)-2-Amino-1-butanol | r-(-)-2 amino-1-
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25ml
A106025-25ml
4
13,90US$
100ml
A106025-100ml
5
33,90US$
500ml
A106025-500ml
1
119,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 10 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
2-Amino-butan-1-ol | 2-Aminobutan-1-ol | 2-Amino-1-butanol, 97% | 1-(r, s)-(hydroxymethyl)propylamine | (?)-2-Amino-1-butanol | SB83767 | (+)-2-Amino-1-butanol | [(1R)-1-(hydroxymethyl)propyl]ammonium | SY049464 | (+/-)-2-Amino-1-butanol | r-(-)-2 amino-1-
Especificaciones y pureza
≥97%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥97%
Nombres e identificadores
Pubchem Sid488182740
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488182740
Sonrisas canónicasCCC(CO)N
IUPAC Name2-aminobutan-1-ol
InChIKeyJCBPETKZIGVZRE-UHFFFAOYSA-N
INCHI1S/C4H11NO/c1-2-4(5)3-6/h4,6H,2-3,5H2,1H3
Isómeros SMILES CCC(CO)N
WGK Alemania 2
RTECS EK9625000
CAS alternativo 13054-87-0
Número ONU 2735
Peso molecular 89.14
Beilstein 4(4)1705
Reaxy-Rn 1098274
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098274&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic nitrogen compounds
ClaseOrganonitrogen compounds
SubclassAmines
Intermediate Tree Nodes Alkanolamines
Direct Parent1,2-aminoalcohols
Alternative Parents Primary alcohols  Organopnictogen compounds  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAliphatic 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
DescripciónThis 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
Estructura 3D
Modelo de Estructura Química Interactiva





Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot NumberCertificate TypeFechaArticulo
H2204243Certificate of AnalysisMay 18, 2026 A106025
H2204244Certificate of AnalysisMay 18, 2026 A106025
H2204246Certificate of AnalysisMay 18, 2026 A106025
E2628205Certificate of AnalysisMar 10, 2026 A106025
G2117043Certificate of AnalysisMay 09, 2025 A106025
G2117046Certificate of AnalysisMay 09, 2025 A106025
B2314057Certificate of AnalysisJul 01, 2021 A106025
B2324120Certificate of AnalysisJul 01, 2021 A106025
Propiedades químicas y físicas
SolubilidadSolubility in water: Completely miscible; Soluble in Alcohol
Índice de refracción1.4508-1.4528
Punto de inflamación (°F)183.2 °F
Punto de inflamación (°C)84℃
Punto de ebullición (°C)177°C
Punto de fusión (°C)-2°C
Peso molecular89.140 g/mol
XLogP3-0.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass89.0841 Da
Monoisotopic Mass89.0841 Da
Topological Polar Surface Area46.300 Ų
Heavy Atom Count6
Formal Charge0
Complexity30.700
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Dong Li, Xiaoying Shang, Wentao Wu, Xiaoqi Li, Zhijin Xu, Lina Li, Maochun Hong, Xueyuan Chen, Junhua Luo.  (2022)  Unprecedented Self-Powered Visible–Infrared Dual-Modal Photodetection Induced by a Bulk Photovoltaic Effect in a Polar Perovskite.  ACS Applied Materials & Interfaces,      [PMID:35044742] [10.1021/acsami.1c21262]
2. Zelalem Anja Zema, Tingting Chen, Hegang Shu, Yingjie Xu.  (2021)  Tuning the CO2 absorption and physicochemical properties of K+ chelated dual functional ionic liquids by changing the structure of primary alkanolamine ligands.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2021.117983]
3. Donghao Liu, Jun Peng, Li Chen, Yan Zhang, Xiaoyang Han, Ping Yang, Hua He.  (2020)  Solid phase extraction-based magnetic carbon nitride/metal organic framework composite with high performance liquid chromatography for the determination of tyrosine kinase inhibitors in urine samples.  Analytical Methods,  12  (39): (4798-4805).  [PMID:32955051] [10.1039/D0AY01243B]
4. 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]
5. Ye Qi, Junwei Ye, Shuangsong Ren, Jialin Lv, Siqi Zhang, Ying Che, Guiling Ning.  (2019)  In-situ synthesis of metal nanoparticles@metal−organic frameworks: Highly effective catalytic performance and synergistic antimicrobial activity.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:31784130] [10.1016/j.jhazmat.2019.121687]
6. 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]
7. Wu Hua-Lei, Zhang Jian-Dong, Zhang Chao-Feng, Fan Xiao-Jun, Chang Hong-Hong, Wei Wen-Long.  (2016)  Characterization of Four New Distinct ω-Transaminases from Pseudomonas putida NBRC 14164 for Kinetic Resolution of Racemic Amines and Amino Alcohols.  APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY,  181  (3): (972-985).  [PMID:27714638] [10.1007/s12010-016-2263-9]
8. Chunping Gao, Qi Shi, Jinxiang Dong.  (2016)  Adsorptive separation performance of 1-butanol onto typical hydrophobic zeolitic imidazolate frameworks (ZIFs).  CRYSTENGCOMM,  18  (21): (3842-3849).  [PMID:] [10.1039/C6CE00249H]
9. Shuofeng Li, Fangfang Wang, Chenhuan Wang, Lin Hao, Ningzhao Shang, Pengbo Zhang, Yawen Zhang, Nuo Xiao, Yaai Kang, Jin Liu, Shutao Gao, Chun Wang, Zhi Wang, Qiuhua Wu.  (2025)  B Doped Zn Single-Atom Nanozyme With Enhanced Oxidase-Like Activity Combined CRISPR/Cas13a System for RNA Sensing.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202418523]
10. 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]
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