p-dimethylaminobenzaldehyde - ≥98% , CAS No.100-10-7

CAS: 100-10-7 Cat. No.: D278973 Formula: (CH₃)₂NC₆H₄CHO Peso molecolare: 149.19 Beilstein Registry Number: 606802 Numero EC: 202-819-0

QUALITÀ & PUREZZA ≥98%

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 |

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Panoramica

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.

Specifiche

Sinonimi

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 |

Specifiche e purezza

≥98%

Meccanismi biochimici e fisiologici

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

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Argon charged

Spedito in

Normal

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

504751358

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504751358

Sorrisi canonici

CN(C)C1=CC=C(C=C1)C=O

IUPAC Name

4-(dimethylamino)benzaldehyde

InChIKey

BGNGWHSBYQYVRX-UHFFFAOYSA-N

INCHI

1S/C9H11NO/c1-10(2)9-5-3-8(7-11)4-6-9/h3-7H,1-2H3

Isomeri SMILES

CN(C)C1=CC=C(C=C1)C=O

WGK Germania

1

Peso molecolare

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=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzoyl derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: 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
• Descrizione: 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

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.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

CYP2A6 Tchem Cytochrome P450 2A6 (1 Activities)

Discover Target: CYP2A6

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

CYP2A13 Tchem Cytochrome P450 2A13 (1 Activities)

Discover Target: CYP2A13

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLC6A1 Tclin GABA transporter 1 (308 Activities)

Discover Target: SLC6A1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MPO Tchem Myeloperoxidase (1002 Activities)

Discover Target: MPO

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CYP2A6 Tchem Cytochrome P450 2A6 (2861 Activities)

Discover Target: CYP2A6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in alcohol, ether, chloroform and acetic acid.
• Sensibilità: Hygroscopic.Light & Air sensitive.
• Punto di infiammabilità (°F): 327.2 °F
• Punto di infiammabilità (°C): 164 °C
• Punto di fusione (°C): 72-75°C
• Peso molecolare: 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