CAS 99-05-8

Acido 3-amminobenzoico

Descrizione:

Acido 3-amminobenzoico, noto anche come acido meta-aminobenzoico, è un'ammina aromatica e un derivato dell'acido benzoico. Presenta un gruppo amino (-NH2) attaccato alla posizione meta dell'anello benzenico rispetto al gruppo acido carbossilico (-COOH). Questo composto è un solido cristallino bianco solubile in acqua e in solventi organici, come etanolo e acetone. Ha un punto di fusione che tipicamente rientra in un intervallo specifico, indicando il suo stato solido a temperatura ambiente. Acido 3-amminobenzoico è noto per il suo ruolo in varie applicazioni, inclusa la sintesi di coloranti, prodotti farmaceutici e come filtro UV nei solari. Inoltre, può agire come indicatore di pH ed è utilizzato nella ricerca biochimica. Il composto presenta proprietà sia acide che basiche grazie alla presenza dei gruppi acido carbossilico e amino, rispettivamente, permettendogli di partecipare a varie reazioni chimiche. I dati di sicurezza indicano che deve essere maneggiato con cura, poiché può causare irritazione al contatto con la pelle o gli occhi.

Formula: C₇H₇NO₂

InChI: InChI=1/C7H7NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,8H2,(H,9,10)/p-1

InChI key: InChIKey=XFDUHJPVQKIXHO-UHFFFAOYSA-N

SMILES: C(O)(=O)C1=CC(N)=CC=C1

Sinonimi:

• 3-Aminobenzenecarboxylic acid
• 3-Aminobenzoate
• 3-Aminobenzoesaeure
• 3-Aminobenzoesaure
• 3-Carboxyaniline
• Acide 3-aminobenzoique
• Acido 3-Aminobenzoico
• Aminobenzoic acid, 3-
• Aniline-3-carboxylic acid
• Benzoic Acid, M-Amino-
• Benzoic acid, 3-amino-
• M-amino benzoic acid
• Nsc 15012
• m-Aminobenzoic acid
• m-Anthranilic acid
• m-Carboxyaniline
• m-Carboxyphenylamine
• 3-Aminobenzoic acid
• AKOS BBS-00004300
• 3-aminobenzoic
• AMINOBENZOIC-3 ACID
• RARECHEM AL BO 0235
• Maba
• 1-AMINO-3-CARBOXYBENZENE
• H-M-ABZ-OH
• H-3-ABZ-OH
• 3-amino-benzoicaci
• Benzoicacid,3-amino-
• aniline-3-carboxylicacid
• m-amino-benzoicaci

3-Aminobenzoic acid, 98%

CAS: 99-05-8

It finds its application as crystalline Intermediate for azo dyes, pharmaceuticals, and X-ray contrast media. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original A

Formula: C₇H₇NO₂

Purezza: 98%

Colore e forma: Pale cream to cream, Powder

Peso molecolare: 137.14

Ref: 02-A19540

M-AMINOBENZOIC ACID

CAS: 99-05-8

Formula: C₇H₇NO₂

Purezza: 98%

Colore e forma: Solid

Peso molecolare: 137.1360

Ref: IN-DA0033LD

3-Aminobenzoic acid

CAS: 99-05-8

3-Aminobenzoic acid ,with CAS No. 99-05-8, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 3-Aminobenzoic acid provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Formula: C₇H₇NO₂

Colore e forma: White Solid

Peso molecolare: 137.13

Ref: TM-PDK0420

3-Aminobenzoic acid

CAS: 99-05-8

Formula: C₇H₇NO₂

Purezza: ≥ 98.0%

Colore e forma: White to off-white crystalline powder

Peso molecolare: 137.14

Ref: 7W-GM3477

Mesalazine (Mesalamine) EP Impurity D

CAS: 99-05-8

Formula: C₇H₇NO₂

Colore e forma: Off-White Solid

Peso molecolare: 137.14

Ref: 4Z-M-1735

3-Aminobenzoic-2,4,5,6-d4 Acid

CAS: 78399-79-8, 99-05-8

Formula: H₂NC₆D₄COOH

Purezza: 99 atom % D

Colore e forma: Off White To Brown Solid

Peso molecolare: 141.07279

Ref: 3U-D7653

3-Aminobenzoic Acid

CAS: 99-05-8

Formula: C₇H₇NO₂

Purezza: >99.0%(T)

Colore e forma: White to Light yellow to Light orange powder to crystal

Peso molecolare: 137.14

Ref: 3B-A0268

3-Aminobenzoic Acid

Prodotto controllato

CAS: 99-05-8

Formula: C₇H₇NO₂

Colore e forma: Neat

Peso molecolare: 137.14

Ref: 86-MM0217.07

3-Aminobenzoic acid

CAS: 99-05-8

3-Aminobenzoic acid

Formula: C₇H₇NO₂

Purezza: 99%

Colore e forma: Pale brown Solid-Powder

Peso molecolare: 137.13597

Ref: 54-OR1944

Mesalazine EP Impurity D

CAS: 99-05-8

Formula: C₇H₇NO₂

Peso molecolare: 137.14

Ref: ST-EA-CP-M11004

3-Aminobenzoic Acid

Prodotto controllato

CAS: 99-05-8

Impurity Mesalazine EP Impurity D
Applications 3-Aminobenzoic Acid, is a chemoattractants against Pseudomonas strains. A reactant used in the preparation of influenza neuraminidase inhibitors, inhibitors of transthyretin amyloid fibril formation and inhibitors of the protein chaperone Hsp90.
References Menzella, H. et al.: J. Med. Chem., 52, 1518 (2009); Johnson, S. et al.: J. Med. Chem., 48, 1576 (2005); Parales, R.: App. Environ. Microbiol., 70, 285 (2004);

Formula: C₇H₇NO₂

Colore e forma: Neat

Peso molecolare: 137.14

Ref: TR-A591490

3-NH2-benzoic acid

CAS: 99-05-8

3-Aminobenzoic acid

Formula: C₇H₇NO₂

Purezza: 97%

Peso molecolare: 137.14

Ref: IN-DG17214

m-Aminobenzoic Acid pure, 98%

CAS: 99-05-8

Formula: C₇H₇NO₂

Purezza: min 98%

Colore e forma: White to Brown, Crystalline powder, Clear, Pale yellow

Peso molecolare: 137.14

Ref: SR-79793

m-Aminobenzoic Acid extrapure AR, 99%

CAS: 99-05-8

Formula: C₇H₇NO₂

Purezza: min. 99%

Colore e forma: White to Brown, Crystalline powder, Clear

Peso molecolare: 137.14

Ref: SR-74004

3-Aminobenzoic acid

CAS: 99-05-8

Formula: C₇H₇NO₂

Purezza: 97%

Colore e forma: Solid, Cream coloured powder

Peso molecolare: 137.138

Ref: 10-F078487

3-Aminobenzoic acid

CAS: 99-05-8

3-Aminobenzoic acid is a cyclic peptide that has been shown to inhibit nitrite ion formation in the human body. Nitrite ions are produced from nitric oxide and bind to hemoglobin, forming methemoglobin. 3-Aminobenzoic acid does not have a direct effect on nitric oxide, but it inhibits the conversion of nitrite ions to nitrate ions by reacting with the hemoglobin in blood. This prevents methemoglobin from being formed and reduces the risk of oxygen deprivation. 3-Aminobenzoic acid is synthesized by humans in response to an infection or other injury and can be found in human serum. The crystal structures of 3-aminobenzoic acid were determined by x-ray crystallography methods, which showed that this molecule forms hydrogen bonds with water molecules. These interactions stabilize its structure and allow for intramolecular hydrogen bonding interactions between its amino acids. The reaction mechanism was determined by kinetic energy

Formula: C₇H₇NO₂

Purezza: Min. 98 Area-%

Colore e forma: Powder

Peso molecolare: 137.14 g/mol

Ref: 3D-FA07680