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· · COA & SDS available for every product · Same-day shipping on in-stock items 3-Aminopropylphosphonic acid - ≥98% , CAS No.13138-33-5
Synonyms
Ethyl 1-N-Boc-3-oxo-piperidine-4-carboxylate | NCGC00015085-03 | NSC 133832 | Lopac0_000080 | NCGC00260765-01 | C3H10NO3P | NCGC00015085-04 | UNII-VM92T06VPB | NCGC00093586-01 | Phosphonic acid, (3-aminopropyl)- | DTXSID50157018 | MFCD00008222 | HMS3260O2
Storage
Room temperature,Argon charged
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Argon charged Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview 3-Aminopropylphosphonic acid was used as a selective antagonist of GABA(C) receptor.
Specifications Synonyms
Ethyl 1-N-Boc-3-oxo-piperidine-4-carboxylate | NCGC00015085-03 | NSC 133832 | Lopac0_000080 | NCGC00260765-01 | C3H10NO3P | NCGC00015085-04 | UNII-VM92T06VPB | NCGC00093586-01 | Phosphonic acid, (3-aminopropyl)- | DTXSID50157018 | MFCD00008222 | HMS3260O2
Specifications & Purity
≥98%
Storage
Room temperature, Argon charged
Names and Identifiers Pubchem Sid 488187061 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488187061 Canonical Smiles C(CN)CP(=O)(O)O IUPAC Name 3-aminopropylphosphonic acid InChIKey GSZQTIFGANBTNF-UHFFFAOYSA-N INCHI 1S/C3H10NO3P/c4-2-1-3-8(5,6)7/h1-4H2,(H2,5,6,7) Isomeric SMILES C(CN)CP(=O)(O)O WGK Germany 3 Molecular Weight 139.09 Reaxy-Rn 1753719 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1753719&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 Kingdom Organic compounds Superclass Organic acids and derivatives Class Organic phosphonic acids and derivatives Subclass Organic phosphonic acids Intermediate Tree Nodes Not available Direct Parent Organic phosphonic acids Alternative Parents Organopnictogen compounds Organophosphorus compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Molecular Framework Aliphatic acyclic compounds Substituents Organophosphonic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organophosphorus compound - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound Description This compound belongs to the class of organic compounds known as organic phosphonic acids. These are organic compounds containing phosphonic acid. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity Air sensitive；Moisture sensitive Melt Point(°C) 294°C Molecular Weight 139.090 g/mol XLogP3 -4.500 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 3 Exact Mass 139.04 Da Monoisotopic Mass 139.04 Da Topological Polar Surface Area 83.600 Ų Heavy Atom Count 8 Formal Charge 0 Complexity 98.700 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Documents & Articles Citations of This Product References 1. Shaocheng Liu, Zhenyu Guo, Xianxin Wu, Xinfeng Liu, Zijian Huang, Liang Li, Jinwen Zhang, Huanping Zhou, Ling-Dong Sun, Chun-Hua Yan. (2022) Zwitterions Narrow Distribution of Perovskite Quantum Wells for Blue Light-Emitting Diodes with Efficiency Exceeding 15%. ADVANCED MATERIALS, 35 (3): (2208078). [PMID:36398427 ] [10.1002/adma.202208078 ] 2. Qingbin Cai, Qin Tan, Jiacheng He, Siyuan Tang, Qiang Sun, Dong He, Tianle Cheng, Guoqiang Ma, Jinfeng Huang, Gangsen Su, Chuanxin Chen, Hao Gu, Bingzhe Wang, Jing Fan, Guichuan Xing, Zhubing He. (2025) Enhancing electron transport for efficiency -recorded HTL-free inverted perovskite solar cells by molecular complementary passivation. Joule, [PMID: [10.1016/j.joule.2025.101880 ] 3. Xufeng Ling, Lin Gui, Yao Wang, Yanhong Fan, Zhilong Zhang, Ru Li, Junjun Guo, Yongjie Wang, Yiping Li, Wei Gong, Guoliang Xiong, Hongyu Wang, Shengdong Cen, Shijian Chen, Jianyu Yuan. (2026) Extrinsic Doping and Interface Engineering of Nonaqueous Tin Oxide Nanocrystals for Efficient Perovskite Solar Cells. ADVANCED FUNCTIONAL MATERIALS, [PMID: [10.1002/adfm.202531734 ]
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