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

CAS: 65-85-0 Cat. No.: B116255 分子式: C7H6O2 分子量: 122.12 Beilstein Registry Number: 636131 EC番号: 200-618-2
844 Citations COA
Benzoic acid - AR, ≥99.5% CAS No(65-85-0) by Aladdin Scientific
注文可能
グレード＆純度 AR ? Analytical Reagent grade — high-purity chemicals meeting strict assay limits for lab analysis. Use when accuracy matters and trace impurities could skew results. ≥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
★
サイズ
USA
ドイツ (EU)*
価格
個数
100g
B116255-100g
在庫あり ≥10
3 在庫あり

$10.90

$16.90
保存 $6.00 (35.50%)
250g
B116255-250g
在庫あり ≥10
2 在庫あり

$14.90

$22.90
保存 $8.00 (34.93%)
500g
B116255-500g
在庫あり ≥10
6 在庫あり

$23.90

$35.90
保存 $12.00 (33.43%)
Enter a quantity for the sizes you want to add.
バルク / カスタム
♡ ウィッシュリスト ⇅ 比較リストに入れる ⎙ ページを印刷
SDS
Safety data
COA
Certificate
DS
データシート
SP
仕様書
仕様 名前と識別子 ドキュメント 詳細データ Taxonomic Classification 3 D構造 関連ターゲット（人間） 関連ターゲット（非人間） 作用メカニズム 証明書（CoA、COO、BSE/TSEと分析図） 化学的性質と物理的性質 よくある質問と記事 Citations of This Product ソリューション計算機 レビュー
🧪
このグレードを選ぶ理由

AR, ≥99.5% AR ベースライン干渉を最小限に抑える必要がある、感度の高いクロマトグラフィーおよび分析ワークフロー向け。

🌡

保管・配送

Room temperature Normal に出荷。正確な仕様については、ロット固有の COA をご確認ください。

📋

品質書類

SDS、COA、データシート、仕様書をダウンロードできます。ロット固有の COA はロット番号検索で入手可能です。

📚

文献的裏付け

クロマトグラフィー、有機合成、クロスカップリング反応に関する 844 件の査読済み論文で引用されています。

仕様

同義語
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]
仕様と純度
AR, ≥99.5%
保管条件
Room temperature
入荷
Normal
等級
AR
純度
≥99.5%
名前と識別子
パブケム・シド
488179505
パブケム・シド・ウル
https://pubchem.ncbi.nlm.nih.gov/substance/488179505
カノニカル・スマイル
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)
異性体SMILES
C1=CC=C(C=C1)C(=O)O
WGKドイツ
1
RTECS
DG0875000
UN番号
UN 1268
包装グループ
I
分子量
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=

ドキュメント

📋 安全データシート（SDS）

危険性、取扱い、保管、および規制遵守を網羅した包括的な文書。

<<<<<<< HEAD SDS をダウンロード → ======= SDS をダウンロード → >>>>>>> release248-p3

✅ 分析証明書（COA）

ロット固有の品質データ。ロット番号を入力して、正確な COA を取得してください。

COA を検索 →

📊 データシート

製品仕様と用途のクイックリファレンス概要。

データシートを見る →

🔬 仕様書

このグレードの完全な品質特性と合格基準。

仕様書を見る →

詳細データ

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
分類Benzene 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
説明This 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
3 D構造
インタラクティブ化学構造モデル





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作用メカニズム
証明書（CoA、COO、BSE/TSEと分析図）
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.

81 results found

Lot NumberCertificate Type日付商品
L2221051L2221051Certificate of AnalysisSep 21, 2026 B116255
L2221047L2221047Certificate of AnalysisSep 21, 2026 B116255
I2615843I2615843Certificate of AnalysisSep 18, 2026 B116255
I2615844I2615844Certificate of AnalysisSep 18, 2026 B116255
I2615849I2615849Certificate of AnalysisSep 18, 2026 B116255
I2615848I2615848Certificate of AnalysisSep 18, 2026 B116255
I2615847I2615847Certificate of AnalysisSep 18, 2026 B116255
I2615846I2615846Certificate of AnalysisSep 18, 2026 B116255
I2615845I2615845Certificate of AnalysisSep 18, 2026 B116255
E2621274E2621274Certificate of AnalysisJun 03, 2026 B116255
E2621286E2621286Certificate of AnalysisJun 03, 2026 B116255
E2621288E2621288Certificate of AnalysisJun 03, 2026 B116255
E2621295E2621295Certificate of AnalysisJun 03, 2026 B116255
A2604256A2604256Certificate of AnalysisJan 09, 2026 B116255
A2604288A2604288Certificate of AnalysisJan 09, 2026 B116255
A2604287A2604287Certificate of AnalysisJan 09, 2026 B116255
A2604286A2604286Certificate of AnalysisJan 09, 2026 B116255
K2527015K2527015Certificate of AnalysisAug 25, 2025 B116255
H2521291H2521291Certificate of AnalysisAug 25, 2025 B116255
H2521290H2521290Certificate of AnalysisAug 25, 2025 B116255
H2521289H2521289Certificate of AnalysisAug 25, 2025 B116255
H2521288H2521288Certificate of AnalysisAug 25, 2025 B116255
H2521286H2521286Certificate of AnalysisAug 25, 2025 B116255
G2610080G2610080Certificate of AnalysisAug 25, 2025 B116255
L2522199L2522199Certificate of AnalysisAug 25, 2025 B116255
D2525237D2525237Certificate of AnalysisMay 08, 2025 B116255
D2525154D2525154Certificate of AnalysisMay 08, 2025 B116255
D2525111D2525111Certificate of AnalysisMay 08, 2025 B116255
D2525110D2525110Certificate of AnalysisMay 08, 2025 B116255
B2506327B2506327Certificate of AnalysisFeb 11, 2025 B116255
B2506329B2506329Certificate of AnalysisFeb 11, 2025 B116255
B2506334B2506334Certificate of AnalysisFeb 11, 2025 B116255
B2506335B2506335Certificate of AnalysisFeb 11, 2025 B116255
B2506336B2506336Certificate of AnalysisFeb 11, 2025 B116255
L2418768L2418768Certificate of AnalysisDec 20, 2024 B116255
L2418722L2418722Certificate of AnalysisDec 20, 2024 B116255
L2418779L2418779Certificate of AnalysisDec 20, 2024 B116255
L2418718L2418718Certificate of AnalysisDec 20, 2024 B116255
J2412403J2412403Certificate of AnalysisOct 19, 2024 B116255
J2412333J2412333Certificate of AnalysisOct 19, 2024 B116255
E2423440E2423440Certificate of AnalysisJun 03, 2024 B116255
E2423175E2423175Certificate of AnalysisJun 03, 2024 B116255
E2423174E2423174Certificate of AnalysisJun 01, 2024 B116255
K2309596K2309596Certificate of AnalysisNov 15, 2023 B116255
K2309595K2309595Certificate of AnalysisNov 15, 2023 B116255
K2309589K2309589Certificate of AnalysisNov 15, 2023 B116255
K2309577K2309577Certificate of AnalysisNov 15, 2023 B116255
K2309576K2309576Certificate of AnalysisNov 15, 2023 B116255
J2311233J2311233Certificate of AnalysisOct 18, 2023 B116255
J2311225J2311225Certificate of AnalysisOct 18, 2023 B116255
J2311224J2311224Certificate of AnalysisOct 18, 2023 B116255
G2326139G2326139Certificate of AnalysisAug 01, 2023 B116255
G2326152G2326152Certificate of AnalysisAug 01, 2023 B116255
G2326141G2326141Certificate of AnalysisAug 01, 2023 B116255
F23061123F23061123Certificate of AnalysisJun 17, 2023 B116255
F23061129F23061129Certificate of AnalysisJun 17, 2023 B116255
F23061070F23061070Certificate of AnalysisJun 17, 2023 B116255
F23061122F23061122Certificate of AnalysisJun 17, 2023 B116255
F23061130F23061130Certificate of AnalysisJun 17, 2023 B116255
C2408173C2408173Certificate of AnalysisJun 17, 2023 B116255
F23061131F23061131Certificate of AnalysisJun 17, 2023 B116255
C2329657C2329657Certificate of AnalysisApr 04, 2023 B116255
C2329655C2329655Certificate of AnalysisApr 04, 2023 B116255
C2329652C2329652Certificate of AnalysisApr 04, 2023 B116255
C2329651C2329651Certificate of AnalysisApr 04, 2023 B116255
C2329650C2329650Certificate of AnalysisApr 04, 2023 B116255
L2221053L2221053Certificate of AnalysisJan 03, 2023 B116255
L2221052L2221052Certificate of AnalysisJan 03, 2023 B116255
L2221048L2221048Certificate of AnalysisJan 03, 2023 B116255
L2221049L2221049Certificate of AnalysisJan 03, 2023 B116255
L2221050L2221050Certificate of AnalysisJan 03, 2023 B116255
H2223250H2223250Certificate of AnalysisAug 30, 2022 B116255
H2223249H2223249Certificate of AnalysisAug 30, 2022 B116255
H2223106H2223106Certificate of AnalysisAug 30, 2022 B116255
H2223251H2223251Certificate of AnalysisAug 30, 2022 B116255
C2209285C2209285Certificate of AnalysisMar 14, 2022 B116255
C2209290C2209290Certificate of AnalysisMar 14, 2022 B116255
C2209268C2209268Certificate of AnalysisMar 14, 2022 B116255
C2209289C2209289Certificate of AnalysisJun 26, 2021 B116255
F2123164F2123164Certificate of AnalysisJun 26, 2021 B116255
C2209269C2209269Certificate of AnalysisJun 26, 2021 B116255
化学的性質と物理的性質
感度Moisture sensitive.
屈折率1.504
沸点（°C）249°C
融点（°C）121-125℃
分子量122.120 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
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Tags:
ATD-DMAP
TCFH–NMI Amidation in Highly Aqueous Media: Research Value, Methodological Understanding, and Experimental Insights
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Amidation reaction TCFH–NMI Amide bond construction
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
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carboxylic acid activation Bromide agent
Reaction Roles of DBU in Different Systems: Experimental Judgment from a Strong Organic Base to Nucleophilic Catalysis and Participation in the Reaction Pathway
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DBU Bicyclic amidine reagents
DMAP Is More Than Just an Organic Base: Experimental Judgment from Nucleophilic Acyl Transfer to Esterification and Macrolactonization
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Organic synthesis Acyl transfer Organic base Esterification
Experimental Selection of SEM-Cl: From O/N-SEM Protection and Directed Functionalization of N-Heterocycles to the Introduction of Protected C1 Fragments
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2-(Trimethylsilyl)ethoxymethyl chloride SEM-Cl
Experimental Evaluation of Triphosgene in Organic Synthesis: Understanding Its Selection Logic Through Reaction Tasks
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Organic synthesis Triphosgene
Triphenylphosphine-Involved Carboxylic Acid Activation and Amide Bond Formation: Activation Pathways, Anhydride Competition, and Applicability Scenarios
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Amide bond formation carboxylic acid activation
Enzymatic Hydroxylation Mechanism of Salicylate Conversion to Catechol
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NADH FAD Salicylate Catechol Salicylate hydroxylase Flavin monooxygenase Decarboxylative hydroxylation Aromatic compound degradation
Alkyd Resins: From Oil/Fatty-Acid-Modified Polyesters to Autoxidative Drying — Understanding Their Structure and Film-Formation Mechanism
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Fatty acid Polyester resin Alkyd
Phenolic-Modified Alkyd Resin: Performance Enhancement and Applications in Fast-Drying Industrial Coatings
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Alkyd Resins Paint Industrial Coatings Film-forming resin
Why Are Preservative Systems in Daily Chemical Products Effective? Common Types, Mechanisms of Action, and Factors Affecting Preservation Efficacy
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Preservatives
Cannizzaro Reaction
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Cannizzaro Reaction
Asymmetric Organocatalysts
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Catalyst Chiral catalyst Organocatalyst Asymmetric
Proline-type Organocatalysts
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Catalyst Chiral catalyst Organocatalyst Asymmetric Proline Prolinol
CTSOBt Benzotriazole–Sulfonate Coupling Reagent: Carboxylic Acid Activation and Synthetic Application Value
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Peptide synthesis coupling reagent coupling reagents
Tea Tree Oil in Skincare: From Chemical Composition and Anti-Acne Mechanisms to Evidence Evaluation and Safe Use
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Tea Tree Oil Skin care products
Structure, Stratum Corneum Distribution, and Stratum Corneum Conditioning Mechanism of Capryloyl Salicylic Acid: Barrier Effects and Safety Evaluation
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Capryloyl Salicylic Acid Lipohydroxy Acid LHA
Strain Release of Azatricycloalkanes: Modular Bridge-Position Functionalization and Stereochemical Control of Three-Dimensional Bridged Aza Scaffolds
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ABCAs azabicyclo[x.1.1]alkanes
Logic for Selecting Amidation Reagents in Aqueous Media: Competing Reactions, Activated Intermediates, and Substrate Effects
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Amidation reaction
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
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Mitsunobu Reaction BEHT Protonated Betaine Alcohol Activation Primary Amines Secondary Amines Bimolecular Nucleophilic Substitution Inversion Of Configuration Α-Chiral Amines
Storage Stability and Deoxyfluorination Reactivity of ImCl[H₂F₃]—Reactivity Modulation of the H₂F₃⁻ Fluoride Source and Substrate Activation by 2-Chloroimidazolium
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Deoxyfluorination
Rotary-Evaporation-Assisted Reversible Dehydration Reactions: Reduced-Pressure Evaporation, Removal of Volatile Components, and Equilibrium Response
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Rotary Evaporation
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