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Basic Description
| Synonyms | 4-(Dimethylamino)benzaldehyde, puriss. p.a., Reag. Ph. Eur., >=99% (perchloric acid titration) | p-Formyl-N,N-dimethylaniline | 4-N,N-DIMETHYLBENZALDEHYDE | 4-(Dimethylamino)benzaldehyde A.C.S. reagent | 4-N,N-Dimethylaminobenzaldehyde | AG-205/03202034 | |
|---|---|
| Specifications & Purity | ≥98% |
| Biochemical and Physiological Mechanisms | 4-(Dimethylamino)benzaldehyde is a simple aldehyde which forms colorful Schiff base adducts with amines, pyrroles and indoles, and can be used to assay proteins for residues containing these functional groups. 4-(Dimethylamino)benzaldehyde is often used f |
| Storage Temp | Argon charged |
| Shipped In | Normal |
| Product Description |
The determination of indole, fecal odor, urine blue mother, tryptophan, albumin, hydrogen peroxide, sodium arsenopyrite, anthranilic acid, antipyrine ergotamine, etc. can also be used to distinguish serum rash from scarlet fever. Make dyes. |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Benzenoids
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Class
Benzene and substituted derivatives
- Subclass Benzoyl derivatives
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Class
Benzene and substituted derivatives
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Superclass
Benzenoids
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzoyl derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzoyl derivatives |
| Alternative Parents | Dialkylarylamines Benzaldehydes Aniline and substituted anilines Organopnictogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzaldehyde - Benzoyl - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Aryl-aldehyde - Tertiary amine - Organic oxide - Aldehyde - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - 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 |
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Associated Targets(Human)
CYP2A6
Tchem
Cytochrome P450 2A6 (1 Activities)
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
CYP2A13
Tchem
Cytochrome P450 2A13 (1 Activities)
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
SLC6A1
Tclin
GABA transporter 1 (308 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
MPO
Tchem
Myeloperoxidase (1002 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
CYP2A6
Tchem
Cytochrome P450 2A6 (2861 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Names and Identifiers
| Pubchem Sid | 504751358 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504751358 |
| IUPAC Name | 4-(dimethylamino)benzaldehyde |
| INCHI | InChI=1S/C9H11NO/c1-10(2)9-5-3-8(7-11)4-6-9/h3-7H,1-2H3 |
| InChIKey | BGNGWHSBYQYVRX-UHFFFAOYSA-N |
| Smiles | CN(C)C1=CC=C(C=C1)C=O |
| Isomeric SMILES | CN(C)C1=CC=C(C=C1)C=O |
| WGK Germany | 1 |
| Molecular Weight | 149.19 |
| Beilstein | 606802 |
| Reaxy-Rn | 606802 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=606802&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.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 C2519393 |
Certificate of Analysis | Apr 01, 2025 | D278973 |
| K2429101 |
Certificate of Analysis | Dec 02, 2024 | D278973 |
| K2407168 |
Certificate of Analysis | Nov 16, 2024 | D278973 |
| I2412032 |
Certificate of Analysis | Sep 18, 2024 | D278973 |
| L2115514 |
Certificate of Analysis | Sep 19, 2023 | D278973 |
| L2115513 |
Certificate of Analysis | Sep 19, 2023 | D278973 |
| L2115516 |
Certificate of Analysis | Sep 13, 2023 | D278973 |
| H2303091 |
Certificate of Analysis | Aug 05, 2023 | D278973 |
| H2303047 |
Certificate of Analysis | Aug 05, 2023 | D278973 |
| D2116216 |
Certificate of Analysis | Jan 15, 2023 | D278973 |
| D2116215 |
Certificate of Analysis | Jan 15, 2023 | D278973 |
| D2116219 |
Certificate of Analysis | Jan 15, 2023 | D278973 |
| D2116218 |
Certificate of Analysis | Jan 15, 2023 | D278973 |
| I2227116 |
Certificate of Analysis | Mar 18, 2021 | D278973 |
| K2228288 |
Certificate of Analysis | Mar 18, 2021 | D278973 |
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Chemical and Physical Properties
| Solubility | Soluble in alcohol, ether, chloroform and acetic acid. |
|---|---|
| Sensitivity | Hygroscopic.Light & Air sensitive. |
| Flash Point(°F) | 327.2 °F |
| Flash Point(°C) | 164 °C |
| Melt Point(°C) | 72-75°C |
| Molecular Weight | 149.190 g/mol |
| XLogP3 | 1.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 149.084 Da |
| Monoisotopic Mass | 149.084 Da |
| Topological Polar Surface Area | 20.300 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 126.000 |
| 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 |
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