Basic Description

Synonyms	AI3-52264 \| Z3034936011 \| 2-Aminobenzaldehyde, >=98% \| ghl.PD_Mitscher_leg0.1278 \| EINECS 208-454-3 \| Benzaldehyde, 2-amino- \| 2-Formylaniline \| EG769PG2AX \| m-Amino benzaldehyde \| 2-ABA \| InChI=1/C7H7NO/c8-7-4-2-1-3-6(7)5-9/h1-5H,8H2 \| Ortho aminobenzald
Specifications & Purity	≥98%
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Reactant for: Preparation of quinoline derivatives as antiviral agents Preparation of electroluminescent materials for OLEDs Friedlander-type synthesis Preparation of 2-tosylaminophenyl cyclopropylmethanols for gold-catalyzed cyclopropyl carbinol rearrangement Benzyl C-H bond amination of arylmethylamines catalyzed by hydroxy-TEMPO Silver-catalyzed aniline mediated cascade hydroamination/cycloaddition reactions.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Benzoyl derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Benzoyl derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Benzoyl derivatives
Alternative Parents	Benzaldehydes Aniline and substituted anilines Vinylogous amides Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Benzaldehyde - Benzoyl - Aniline or substituted anilines - Aryl-aldehyde - Vinylogous amide - Hydrocarbon derivative - Organopnictogen compound - Aldehyde - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Organic oxide - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as benzoyl derivatives. These are organic compounds containing an acyl moiety of benzoic acid with the formula (C6H5CO-).
External Descriptors	Not available
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. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	488184112
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488184112
IUPAC Name	2-aminobenzaldehyde
INCHI	InChI=1S/C7H7NO/c8-7-4-2-1-3-6(7)5-9/h1-5H,8H2
InChIKey	FXWFZIRWWNPPOV-UHFFFAOYSA-N
Smiles	C1=CC=C(C(=C1)C=O)N
Isomeric SMILES	C1=CC=C(C(=C1)C=O)N
WGK Germany	3
Molecular Weight	121.14
Reaxy-Rn	507154
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=507154&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.

29 results found

Lot Number	Certificate Type	Date	Item
F2516075	Certificate of Analysis	May 12, 2025	A100686
H2310039	Certificate of Analysis	May 12, 2025	A100686
H2310049	Certificate of Analysis	May 12, 2025	A100686
H2310034	Certificate of Analysis	May 12, 2025	A100686
H2310044	Certificate of Analysis	May 12, 2025	A100686
H2310040	Certificate of Analysis	May 12, 2025	A100686
H2310070	Certificate of Analysis	May 12, 2025	A100686
H2310048	Certificate of Analysis	May 12, 2025	A100686
H2310046	Certificate of Analysis	May 12, 2025	A100686
J2416370	Certificate of Analysis	Sep 26, 2024	A100686
J2416372	Certificate of Analysis	Sep 26, 2024	A100686
J2411419	Certificate of Analysis	Sep 26, 2024	A100686
J2411420	Certificate of Analysis	Sep 26, 2024	A100686
J2416371	Certificate of Analysis	Sep 26, 2024	A100686
J2411423	Certificate of Analysis	Sep 26, 2024	A100686
J2411424	Certificate of Analysis	Sep 26, 2024	A100686
J2411425	Certificate of Analysis	Sep 26, 2024	A100686
J2411426	Certificate of Analysis	Sep 26, 2024	A100686
J2416369	Certificate of Analysis	Sep 26, 2024	A100686
H2310024	Certificate of Analysis	Jul 07, 2023	A100686
H2310042	Certificate of Analysis	Jul 07, 2023	A100686
C2324491	Certificate of Analysis	Apr 11, 2023	A100686
C2324488	Certificate of Analysis	Apr 11, 2023	A100686
C2324486	Certificate of Analysis	Apr 11, 2023	A100686
C2324494	Certificate of Analysis	Apr 11, 2023	A100686
C2324484	Certificate of Analysis	Apr 11, 2023	A100686
C2324489	Certificate of Analysis	Apr 11, 2023	A100686
C2324490	Certificate of Analysis	Apr 11, 2023	A100686
C2324475	Certificate of Analysis	Apr 11, 2023	A100686

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Chemical and Physical Properties

Solubility	Soluble in ethanol (25 mg/ml).
Flash Point(°F)	235.4 °F
Flash Point(°C)	113 °C
Melt Point(°C)	39-40°C
Molecular Weight	121.140 g/mol
XLogP3	1.600
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	1
Exact Mass	121.053 Da
Monoisotopic Mass	121.053 Da
Topological Polar Surface Area	43.100 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	103.000
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

How to Cite Aladdin Scientific Products?

1. Lihua Zhu, Huan Zhang, Huaze Zhu, Huan Fu, Anna Kroner, Zhiqing Yang, Hengqiang Ye, Bing Hui Chen, Rafael Luque. (2022) Controlling nanostructures of PtNiCo/C trimetallic nanocatalysts and relationship of structure-catalytic performance for selective hydrogenation of nitroarenes. JOURNAL OF CATALYSIS, 413 (978).

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SKU	Size	Availability	Price
A100686-250mg	250mg	2	$9.90
A100686-1g	1g	8	$12.90
A100686-5g	5g	4	$25.90
A100686-10g	10g	3	$45.90
A100686-25g	25g	1	$109.90
A100686-100g	100g	1	$417.90

2-Aminobenzaldehyde - 98%, high purity , CAS No.529-23-7