Determine the necessary mass, volume, or concentration for preparing a solution.
This is a demo store. No orders will be fulfilled.
| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
|
A107272-1g
|
1g |
1
|
$9.90
|
|
|
A107272-5g
|
5g |
2
|
$14.90
|
|
|
A107272-10g
|
10g |
3
|
$24.90
|
|
|
A107272-25g
|
25g |
1
|
$49.90
|
|
|
A107272-100g
|
100g |
1
|
$139.90
|
|
|
A107272-500g
|
500g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
|
$499.90
|
|
| Synonyms | Benzyl alcohol, p-amino- | AC-23679 | HY-W007465 | (4-amino phenyl)methanol | CK2439 | PS-6145 | A8610 | SY015076 | 4-hydroxymethylphenylamine | A1096 | 4-aminophenylmethanol | AKOS005203356 | BCP27029 | 4-Aminobenzyl alcohol | 4-amino-benzyl alcohol | BP |
|---|---|
| Specifications & Purity | ≥98% |
| Storage Temp | Store at -20°C,Argon charged |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Product Description |
4-Aminobenzyl alcohol is used as a starting material to synthesize other organic compounds. Application: 4-Aminobenzyl alcohol can be used: |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzyl alcohols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzyl alcohols |
| Alternative Parents | Aniline and substituted anilines Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives Aromatic alcohols |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Aniline or substituted anilines - Benzyl alcohol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic alcohol - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzyl alcohols. These are organic compounds containing the phenylmethanol substructure. |
| External Descriptors | a small molecule |
|
|
|
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| IUPAC Name | (4-aminophenyl)methanol |
|---|---|
| INCHI | InChI=1S/C7H9NO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5,8H2 |
| InChIKey | AXKGIPZJYUNAIW-UHFFFAOYSA-N |
| Smiles | C1=CC(=CC=C1CO)N |
| Isomeric SMILES | C1=CC(=CC=C1CO)N |
| WGK Germany | 3 |
| Molecular Weight | 123.15 |
| Beilstein | 2078680 |
| Reaxy-Rn | 2078680 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2078680&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Nov 30, 2024 | A107272 | |
| Certificate of Analysis | Nov 30, 2024 | A107272 | |
| Certificate of Analysis | Nov 30, 2024 | A107272 | |
| Certificate of Analysis | Nov 30, 2024 | A107272 | |
| Certificate of Analysis | Jul 18, 2024 | A107272 | |
| Certificate of Analysis | Mar 08, 2024 | A107272 | |
| Certificate of Analysis | Mar 08, 2024 | A107272 | |
| Certificate of Analysis | Oct 20, 2023 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Oct 15, 2022 | A107272 | |
| Certificate of Analysis | Jun 27, 2022 | A107272 |
| Solubility | Soluble in alcohol, ether and benzene. Partially soluble in water. |
|---|---|
| Sensitivity | Air & Heat & Light sensitive |
| Boil Point(°C) | 171°C/11mmHg |
| Melt Point(°C) | 60-65°C |
| Molecular Weight | 123.150 g/mol |
| XLogP3 | -0.200 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 1 |
| Exact Mass | 123.068 Da |
| Monoisotopic Mass | 123.068 Da |
| Topological Polar Surface Area | 46.300 Ų |
| Heavy Atom Count | 9 |
| Formal Charge | 0 |
| Complexity | 77.000 |
| 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 |
| 1. Yutong Shao, Miaomiao Chen, Wenlong Chen, Zehui Wang, Mengzhang Sui, Mingyu Tian, Yingnan Wu, Jitao Song, Debin Ji, Fengling Song. (2023) Integration of Activation by Hypoxia and Inhibition Resistance of Tumor cells to Apoptosis for Precise and Augmented Photodynamic Therapy. Advanced Healthcare Materials, (2300503). |
| 2. Hong Liu, Ren Zhu, Nannan Shi, Long Zhang, Shun Li, Jianming Zhang. (2022) Piezotronic Effect Induced Schottky Barrier Decrease to Boost the Plasmonic Charge Separation of BaTiO3-Au Heterojunction for the Photocatalytic Selective Oxidation of Aminobenzyl Alcohol. ACS Applied Materials & Interfaces, 14 (50): (55548–55558). |
| 3. Jiahui Gu, Hong Liu, Tingyu Peng, Shun Li, Li Xu, Jianming Zhang, Long Zhang. (2022) Ag@CeO2–Au Nanorod Plasmonic Nanohybrids for Enhanced Photocatalytic Conversion of Benzyl Alcohol to Benzaldehyde. ACS Applied Nano Materials, 5 (4): (4972–4982). |
| 4. Ruirui Cao, Sai Chen, Huanbing Liu, Haihui Liu, Xingxiang Zhang. (2018) Fabrication and characterization of thermo-responsive GO nanosheets with controllable grafting of poly(hexadecyl acrylate) chains. JOURNAL OF MATERIALS SCIENCE, 53 (6): (4103-4117). |
| 5. Peilian Liu, Bowen Li, Chenyue Zhan, Fang Zeng, Shuizhu Wu. (2017) A two-photon-activated prodrug for therapy and drug release monitoring. Journal of Materials Chemistry B, 5 (36): (7538-7546). |
| 6. Dandan Wu, Yanqiao Zhang, Ming Wen, Hao Fang, Qingsheng Wu. (2017) Fe3O4/FeNi Embedded Nanostructure and Its Kinetic Law for Selective Catalytic Reduction of p-Nitrophenyl Compounds. INORGANIC CHEMISTRY, 56 (9): (5152–5157). |
| 7. Xiangfei Han, Jinling Chen, Mengjuan Jiang, Na Zhang, Kexin Na, Cong Luo, Ruoshi Zhang, Mengchi Sun, Guimei Lin, Rong Zhang, Yan Ma, Dan Liu, Yongjun Wang. (2016) Paclitaxel–Paclitaxel Prodrug Nanoassembly as a Versatile Nanoplatform for Combinational Cancer Therapy. ACS Applied Materials & Interfaces, 8 (49): (33506–33513). |
| 8. Hao Fang, Ming Wen, Hanxing Chen, Qingsheng Wu, Weiying Li. (2015) Graphene stabilized ultra-small CuNi nanocomposite with high activity and recyclability toward catalysing the reduction of aromatic nitro-compounds. Nanoscale, 8 (1): (536-542). |
| 9. Peisheng Zhang, Xiao-fang Jiang, Xuezheng Nie, Yong Huang, Fang Zeng, Xitao Xia, Shuizhu Wu. (2016) A two-photon fluorescent sensor revealing drug-induced liver injury via tracking γ-glutamyltranspeptidase (GGT) level in vivo. BIOMATERIALS, 80 (46). |
| 10. Chunlei Li, Shun Li, Long Zhao, Jianming Zhang. (2024) Bi2Te3/Carbon Nanotube Hybrid Nanomaterials as Catalysts for Thermoelectric Hydrogen Peroxide Generation. MOLECULES, 29 (22): (5242). |
| 11. Wen-Wang Yu, Xiang-Guang Meng, Wen Li, Li-Yu Chen, Zi-Yu Gan, Yu-Lian Zhang, Jie Zhou. (2024) Highly efficient capture and conversion of CO2 into cyclic carbonates from actual flue gas under atmospheric pressure. Journal of Environmental Chemical Engineering, 12 (113614). |
| 12. Lixia Guo, Yafei Tian, Liang Zhou, Shiyue Kang, Chengwu Zhang, Wen Liu, Haipeng Diao, Liheng Feng. (2024) Tailored Phototherapy Agent by Infection Site In Situ Activated Against Methicillin-Resistant S. aureus. Advanced Healthcare Materials, (2400593). |