CAS 56-91-7
:4-(Aminomethyl)benzoic acid
Description:
4-(Aminomethyl)benzoic acid, also known as p-aminobenzylcarboxylic acid, is an aromatic amino acid characterized by the presence of both an amino group (-NH2) and a carboxylic acid group (-COOH) attached to a benzene ring. This compound typically appears as a white to off-white crystalline solid and is soluble in water, reflecting its polar functional groups. It has a melting point that varies depending on purity and form, and it is known for its role in various chemical syntheses and applications, particularly in pharmaceuticals and as a building block in organic chemistry. The amino group can participate in various reactions, including amide formation and coupling reactions, making it versatile in synthetic pathways. Additionally, 4-(Aminomethyl)benzoic acid can exhibit biological activity, which may be of interest in medicinal chemistry. Its CAS number, 56-91-7, is a unique identifier that facilitates its recognition in chemical databases and regulatory frameworks.
Formula:C8H9NO2
InChI:InChI=1S/C8H9NO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4H,5,9H2,(H,10,11)
InChI key:InChIKey=QCTBMLYLENLHLA-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=CC=C(CN)C=C1
Synonyms:- 4-(Aminomethyl)benzoic acid
- 4-Carboxybenzylamine
- Benzoic acid, 4-(aminomethyl)-
- Benzylamine-4-carboxylic acid
- Gumbix
- NSC 41629
- Pamba
- Styptopur
- p-(Aminomethyl)benzoic acid
- p-Carboxybenzylamine
- p-Toluic acid, α-amino-
- α-Amino-p-toluic acid
- 4-Aminomethylbenzoic acid
- 4-CARBOXYLBENZYLAMINE
- H-4-AMB-OH
- AMINOMETHYL BENZOIC ACID
- NH2-CH2-PH(4)-COOH
- H-(4)AMBZ-OH
- Aminomethylbenzoic acid CP2000
- TIMTEC-BB SBB006704
- Benzoic acid, 4-(aminomethyl)-(9CI)
- -Amino-p-toluicacid
- 4-Aminomethylbenzonium acid
- p-Aminomethylbenzoic
- 4-(AMINOMETHYL)BENZOIC ACIDTRANEXAMIC ACID
- RARECHEM AL BW 0005
- See more synonyms
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Found 14 products.
4-(Aminomethyl)benzoic acid, 97%
CAS:<p>4-(Aminomethyl)benzoic acid acts as an unnatural amino acid derivative. It is also used as a type 2 antifibrinolytic agent. Further, it reacts with 2-methyl-isothiourea sulfate to prepare 4-guanidinomethylbenzoic acid. This Thermo Scientific Chemicals brand product was originally part of the Alfa Ae</p>Formula:C8H9NO2Purity:97%Color and Shape:White to cream, PowderMolecular weight:151.174-(Aminomethyl)Benzoic Acid
CAS:Formula:C8H9NO2Purity:98%Color and Shape:SolidMolecular weight:151.16264-(Aminomethyl)benzoic acid
CAS:4-(Aminomethyl)benzoic acid (PAMBA), an antifibrinolytic, is an unnatural amino acid derivative.Formula:C8H9NO2Purity:99.55% - 99.64%Color and Shape:White To Light Yellow Crystal PowderMolecular weight:151.16Tranexamic Acid EP Impurity D
CAS:Formula:C8H9NO2Color and Shape:White To Off-White SolidMolecular weight:151.174-(Aminomethyl)benzoic acid
CAS:Formula:C8H9NO2Purity:(HPLC) ≥ 98.0%Color and Shape:White to off-white powderMolecular weight:151.164-(Aminomethyl)benzoic acid
CAS:4-(Aminomethyl)benzoic acidFormula:C8H9NO2Purity:98%Color and Shape: white solidMolecular weight:151.16g/mol4-(Aminomethyl)benzoic Acid
CAS:Formula:C8H9NO2Purity:>97.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:151.174-Aminomethylbenzoic Acid
CAS:Controlled ProductFormula:C8H9NO2Color and Shape:NeatMolecular weight:151.164-(Aminomethyl)benzoic Acid
CAS:Controlled Product<p>Impurity Tranexamic EP Impurity D<br>Applications 4-(Aminomethyl)benzoic Acid (Tranexamic EP Impurity D) is a type 2 antifibrinolytic agent.<br>References Markwardt, F., et al.: Prog. Fibrinolysis. 5, 178 (1981); Markswardt, F.. et al.: Thrombosis. Res., 9, 143 (1976);<br></p>Formula:C8H9NO2Color and Shape:WhiteMolecular weight:151.164-Aminomethylbenzoic acid
CAS:<p>4-Aminomethylbenzoic acid (4AMBA) is a metabolite that is formed from the amino acid methionine. It has been shown to inhibit the growth of prostate cancer cells in vitro and in vivo. 4-Aminomethylbenzoic acid inhibits the activity of polymerase chain reaction (PCR), which is an enzyme that catalyzes DNA replication. The hydroxyl group on 4-aminomethylbenzoic acid reacts with one of the phosphate groups on DNA, forming a covalent bond and inhibiting DNA synthesis. This inhibition occurs at the step called initiation, where DNA synthesis begins by binding of RNA polymerase to a specific sequence of DNA. In addition, 4-aminomethylbenzoic acid also inhibits the activity of x-ray diffraction data, which is an enzyme that catalyzes RNA transcription. Histological analysis shows that 4-aminomethylbenzoic acid causes congestive heart</p>Formula:C8H9NO2Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:151.16 g/mol4-(Aminomethyl)benzoic acid
CAS:Formula:C8H9NO2Purity:98%Color and Shape:SolidMolecular weight:151.165













