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4-Aminobenzyl alcohol - 98%, high purity , CAS No.623-04-1

    Grade & Purity:
  • ≥98%
In stock
Item Number
A107272
Grouped product items
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

Basic Description

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:
In the synthesis of 4-{N-[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutylamino}benzyl ester.
As a reactant to synthesize cross-azo compounds and cathepsin B cleavable dipeptide linker.
As a starting material to synthesize hydrogelators for drug delivery applications.

Taxonomic Classification

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

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

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=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

18 results found

Lot Number Certificate Type Date Item
L2420292 Certificate of Analysis Nov 30, 2024 A107272
L2420300 Certificate of Analysis Nov 30, 2024 A107272
L2420301 Certificate of Analysis Nov 30, 2024 A107272
L2420302 Certificate of Analysis Nov 30, 2024 A107272
K2419191 Certificate of Analysis Jul 18, 2024 A107272
D2407099 Certificate of Analysis Mar 08, 2024 A107272
D2407098 Certificate of Analysis Mar 08, 2024 A107272
L1919024 Certificate of Analysis Oct 20, 2023 A107272
J2229013 Certificate of Analysis Oct 15, 2022 A107272
J2229041 Certificate of Analysis Oct 15, 2022 A107272
J2229031 Certificate of Analysis Oct 15, 2022 A107272
J2316003 Certificate of Analysis Oct 15, 2022 A107272
H2420049 Certificate of Analysis Oct 15, 2022 A107272
J2229014 Certificate of Analysis Oct 15, 2022 A107272
G2307498 Certificate of Analysis Oct 15, 2022 A107272
C2310626 Certificate of Analysis Oct 15, 2022 A107272
B2426252 Certificate of Analysis Oct 15, 2022 A107272
H1829106 Certificate of Analysis Jun 27, 2022 A107272

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Chemical and Physical Properties

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

Citations of This Product

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,  (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,  (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,  (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,  (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). 

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