Benzoic acid - ACS, ≥99.5% , CAS No.65-85-0

CAS: 65-85-0 Cat. No.: B116259 Fórmula: C7H6O2 Peso molecular: 122.12 Beilstein Registry Number: 636131 Número EC: 200-618-2
Disponible para pedir
CALIDAD & PUREZA ACS ? ACS grade — meets American Chemical Society specifications, the analytical benchmark in the US. Use for analytical and QC work needing ACS-defined purity. ≥99.5%
Synonyms
Eyelids Wipes | Benzoic acid (USP:JAN) | Benzoic acid [USP:JAN] | NSC7918 | Benzenecarboxylate | Benzoic Acid 2000 microg/mL in Dichloromethane | FEMA No. 2131 | NSC 149 | Acid, Benzoic | AI3-03710 | Benzoicum Ac | CARBOXYLBENZENE | BENZOIC ACID [USP-RS]
Storage
Room temperature
Shipped In
Normal
★
Talla
USA
Alemania (EU)*
Precio
Cantidad
100g
B116259-100g
Fabricado bajo pedido en EE. UU. · 2–4 semanas ·
—

20,90US$

25,90US$
Guardar 5,00 US$ (19.31%)
250g
B116259-250g
Disponible ≥10
—
41,90US$
500g
B116259-500g
3 Disponible
—
57,90US$
Enter a quantity for the sizes you want to add.
🧪
Por qué esta calidad

ACS, ≥99.5% ACS para flujos de trabajo cromatográficos y analíticos sensibles que requieren una interferencia mínima de la línea base.

🌡

Almacenamiento y envío

Room temperature Envío Normal. Consulte el COA específico del lote para conocer las especificaciones exactas.

📋

Documentos de calidad

SDS, COA, ficha técnica y hoja de especificaciones disponibles para descargar. COA específico del lote accesible mediante búsqueda por número de lote.

📚

Prueba documental

Citado en 844 publicaciones revisadas por pares sobre cromatografía, síntesis orgánica y reacciones de acoplamiento cruzado.

Especificaciones

Sinónimos
Eyelids Wipes | Benzoic acid (USP:JAN) | Benzoic acid [USP:JAN] | NSC7918 | Benzenecarboxylate | Benzoic Acid 2000 microg/mL in Dichloromethane | FEMA No. 2131 | NSC 149 | Acid, Benzoic | AI3-03710 | Benzoicum Ac | CARBOXYLBENZENE | BENZOIC ACID [USP-RS]
Especificaciones y pureza
ACS, ≥99.5%
Mecanismos bioquímicos y fisiológicos
Benzoic acid is a weak acid that is a precursor for the synthesis of many important organic compounds. L. monocytogens has displayed an acid adaption to the presence of Benzoic acid with a decrease in total lipid phosphorus.
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
ACS
Pureza
≥99.5%
Nombres e identificadores
Sonrisas canónicas
C1=CC=C(C=C1)C(=O)O
IUPAC Name
benzoic acid
InChIKey
WPYMKLBDIGXBTP-UHFFFAOYSA-N
INCHI
1S/C7H6O2/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H,8,9)
Isómeros SMILES
C1=CC=C(C=C1)C(=O)O
WGK Alemania
1
RTECS
DG0875000
Número ONU
UN 1268
Grupo de embalaje
I
Peso molecular
122.12
Beilstein
636131
Reaxy-Rn
636131
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636131&ln=

Documentación

📋 Hoja de datos de seguridad (SDS)

Documento completo sobre peligros, manipulación, almacenamiento y cumplimiento normativo.

<<<<<<< HEAD Descargar SDS → ======= Descargar SDS → >>>>>>> release248-p3

✅ Certificado de análisis (COA)

Datos de calidad específicos del lote. Introduzca su número de lote para obtener el COA exacto.

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📊 Ficha técnica

Resumen de referencia rápida de las especificaciones y aplicaciones del producto.

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🔬 Hoja de especificaciones

Atributos de calidad completos y criterios de aceptación para esta calidad.

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Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentBenzoic acids
Alternative Parents Benzoyl derivatives  Monocarboxylic acids and derivatives  Carboxylic acids  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzoic acid - Benzoyl - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as benzoic acids. These are organic Compounds containing a benzene ring which bears at least one carboxyl group.
External Descriptors benzoic acids
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
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ESR1 Tclin Estrogen receptor alpha (17718 Activities)
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HMGCR Tclin HMG-CoA reductase (2475 Activities)
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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
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INSR Tclin Insulin receptor (5558 Activities)
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PGR Tclin Progesterone receptor (8562 Activities)
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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
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AR Tclin Androgen Receptor (11781 Activities)
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ACE Tclin Angiotensin-converting enzyme (1423 Activities)
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DRD2 Tclin Dopamine D2 receptor (23596 Activities)
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TYR Tclin Tyrosinase (717 Activities)
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GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
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TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
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DRD1 Tclin Dopamine D1 receptor (9720 Activities)
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DRD4 Tchem Dopamine D4 receptor (7907 Activities)
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ACHE Tclin Acetylcholinesterase (18204 Activities)
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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
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HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC18A2 Tclin Synaptic vesicular amine transporter (118 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
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Staphylococcus aureus (210822 Activities)
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Mycobacterium tuberculosis (203094 Activities)
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Saccharomyces cerevisiae (19171 Activities)
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Mycobacterium tuberculosis variant bovis (1746 Activities)
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Caenorhabditis elegans (1055 Activities)
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Meloidogyne incognita (862 Activities)
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Mus musculus (284745 Activities)
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Rattus norvegicus (775804 Activities)
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lef Anthrax lethal factor (7585 Activities)
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Radish (446 Activities)
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norA Quinolone resistance protein norA (2171 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Slc22a20 Solute carrier family 22 member 20 (86 Activities)
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Slc22a6 Solute carrier family 22 member 6 (141 Activities)
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Curvularia lunata (722 Activities)
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Lolium rigidum (323 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

38 results found

Lot NumberCertificate TypeFechaArticulo
L2221056L2221056Certificate of AnalysisSep 21, 2026 B116259
L2221057L2221057Certificate of AnalysisSep 21, 2026 B116259
A2605005A2605005Certificate of AnalysisDec 22, 2025 B116259
E2621297E2621297Certificate of AnalysisDec 22, 2025 B116259
E2621275E2621275Certificate of AnalysisDec 22, 2025 B116259
H2613057H2613057Certificate of AnalysisDec 22, 2025 B116259
A2604289A2604289Certificate of AnalysisDec 22, 2025 B116259
C2209271C2209271Certificate of AnalysisDec 10, 2025 B116259
L2115457L2115457Certificate of AnalysisSep 17, 2025 B116259
H2521287H2521287Certificate of AnalysisJul 11, 2025 B116259
H2521285H2521285Certificate of AnalysisJul 11, 2025 B116259
F2123182F2123182Certificate of AnalysisApr 03, 2025 B116259
D2525217D2525217Certificate of AnalysisMar 28, 2025 B116259
B2506334B2506334Certificate of AnalysisDec 30, 2024 B116259
B2506323B2506323Certificate of AnalysisDec 30, 2024 B116259
J2412334J2412334Certificate of AnalysisSep 23, 2024 B116259
J2412375J2412375Certificate of AnalysisSep 23, 2024 B116259
E2423176E2423176Certificate of AnalysisMay 08, 2024 B116259
F23061137F23061137Certificate of AnalysisMay 19, 2023 B116259
F23061141F23061141Certificate of AnalysisMay 19, 2023 B116259
F23061128F23061128Certificate of AnalysisMay 19, 2023 B116259
G2326142G2326142Certificate of AnalysisMay 19, 2023 B116259
G2326149G2326149Certificate of AnalysisMay 19, 2023 B116259
F23061127F23061127Certificate of AnalysisMay 19, 2023 B116259
C2330042C2330042Certificate of AnalysisFeb 27, 2023 B116259
C2329656C2329656Certificate of AnalysisFeb 27, 2023 B116259
L2221055L2221055Certificate of AnalysisOct 11, 2022 B116259
L2221054L2221054Certificate of AnalysisOct 11, 2022 B116259
L2221058L2221058Certificate of AnalysisOct 11, 2022 B116259
L2221059L2221059Certificate of AnalysisOct 11, 2022 B116259
K2528118K2528118Certificate of AnalysisOct 11, 2022 B116259
H2223248H2223248Certificate of AnalysisJun 27, 2022 B116259
H2223247H2223247Certificate of AnalysisJun 27, 2022 B116259
H2223245H2223245Certificate of AnalysisJun 27, 2022 B116259
E2225001E2225001Certificate of AnalysisJun 04, 2022 B116259
G2205168G2205168Certificate of AnalysisJan 24, 2022 B116259
C2209291C2209291Certificate of AnalysisJan 24, 2022 B116259
C2209286C2209286Certificate of AnalysisJan 24, 2022 B116259
Propiedades químicas y físicas
SolubilidadSoluble in ethanol (100 mg/ml), water (3.5 mg/ml at 25 °C), chloroform (15 mg/ml), methanol (71.5 mg/ml), and hexane (0.9 mg/ml).
SensibilidadMoisture sensitive.
Índice de refracción1.504
Punto de ebullición (°C)249°C
Punto de fusión (°C)121-125℃
Peso molecular122.120 g/mol
XLogP31.900
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass122.037 Da
Monoisotopic Mass122.037 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count9
Formal Charge0
Complexity103.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Asymmetric Organocatalysts
Proline-type Organocatalysts
1,3-Dibromo-5,5-Dimethylhydantoin, DBDMH
How Organic Acids “Stabilize a System”: Selection Logic via the pH Window, Salt Forms, and Metal-Ion Management (with a navigation guide to Tables A–E)
β-Acyloxy Alkenyl Amides (AAAs): A New Approach to Amide Bond and Peptide Bond Construction Worth Attention
Revisiting Titanium Tetrachloride: New Advances in the Direct Amidation and Esterification of Carboxylic Acids
DAST-Mediated Amidation at Room Temperature: Method Features, Practical Value, and Scope of Applicability
Understanding ATD-DMAP: From Reagent Design to Esterification, Amidation, and Stereochemical Integrity
TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights
Triphenylphosphine Dibromide (PPh₃Br₂) Is More Than Just a Brominating Reagent: Experimental Selection Logic from Alcohol-to-Alkyl Bromide Conversion to Carboxylic Acid Activation and One-Pot Esterification, Vinyl Bromide Formation, and Nitrile Constructi
Reaction Roles of DBU in Different Systems: Experimental Judgment from a Strong Organic Base to Nucleophilic Catalysis and Participation in the Reaction Pathway
DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization
Experimental Selection of SEM-Cl: From O/N-SEM Protection and Directed Functionalization of N-Heterocycles to the Introduction of Protected C1 Fragments
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
Enzymatic Hydroxylation Mechanism of Salicylate Conversion to Catechol
Alkyd Resins: From Oil/Fatty-Acid-Modified Polyesters to Autoxidative Drying — Understanding Their Structure and Film-Formation Mechanism
Phenolic-Modified Alkyd Resin: Performance Enhancement and Applications in Fast-Drying Industrial Coatings
Why Are Preservative Systems in Daily Chemical Products Effective? Common Types, Mechanisms of Action, and Factors Affecting Preservation Efficacy
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
Tea Tree Oil in Skincare: From Chemical Composition and Anti-Acne Mechanisms to Evidence Evaluation and Safe Use
Structure, Stratum Corneum Distribution, and Stratum Corneum Conditioning Mechanism of Capryloyl Salicylic Acid: Barrier Effects and Safety Evaluation
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects
Why Primary and Secondary Amines Have Difficulty Participating Directly in the Classical Mitsunobu Reaction: Mechanism, Inversion of Configuration, and Reaction Scope of BEHT-Mediated Alcohol Amination
Storage Stability and Deoxyfluorination Reactivity of ImCl[H₂F₃]—Reactivity Modulation of the H₂F₃⁻ Fluoride Source and Substrate Activation by 2-Chloroimidazolium
Rotary-Evaporation-Assisted Reversible Dehydration Reactions: Reduced-Pressure Evaporation, Removal of Volatile Components, and Equilibrium Response
Citations of This Product
Calculadoras de soluciones
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