Benzohydroxamic Acid - ≥98%(T) , CAS No.495-18-1

CAS: 495-18-1 Cat. No.: B152659 Molecular Weight: 137.14 EC Number: 207-797-6
AVAILABLE TO ORDER
GRADE & PURITY ≥98%(T)
Synonyms
Benzohyroxamate | N-Hydroxybenzamide | henylhydroxamic acid
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
B152659-1g
2
$9.90
5g
B152659-5g
3
$10.90
25g
B152659-25g
3
$24.90
100g
B152659-100g
2
$79.90
500g
B152659-500g
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$319.90
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Why this grade

≥98%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 18 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
Benzohyroxamate | N-Hydroxybenzamide | henylhydroxamic acid
Specifications & Purity
≥98%(T)
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Purity
≥98%(T)
Names and Identifiers
Pubchem Sid504751928
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751928
Canonical SmilesC1=CC=C(C=C1)C(=O)NO
IUPAC NameN-hydroxybenzamide
InChIKeyVDEUYMSGMPQMIK-UHFFFAOYSA-N
INCHI1S/C7H7NO2/c9-7(8-10)6-4-2-1-3-5-6/h1-5,10H,(H,8,9)
Isomeric SMILES C1=CC=C(C=C1)C(=O)NO
WGK Germany 3
RTECS DF9650000
Molecular Weight 137.14
Reaxy-Rn 1907585
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1907585&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentBenzoic acids and derivatives
Alternative Parents Benzoyl derivatives  Hydroxamic acids  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzoic acid or derivatives - Benzoyl - Hydroxamic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzoic acids and derivatives. These are organic compounds containing a carboxylic acid substituent attached to a benzene ring.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
HDAC6 Tclin Histone deacetylase 6 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC8 Tclin Histone deacetylase 8 (4516 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MMP3 Tchem Matrix metalloproteinase 3 (3433 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC2 Tclin Histone deacetylase 2 (3971 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC3 Tclin Histone deacetylase 3 (3654 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC4 Tclin Histone deacetylase 4 (2328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC9 Tclin Histone deacetylase 9 (708 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC7 Tclin Histone deacetylase 7 (1047 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IDO1 Tchem Indoleamine 2,3-dioxygenase (6650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HDAC3 Tclin Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2) (735 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
blaZ Beta-lactamase (285 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac1 Histone deacetylase 1 (93 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac5 Histone deacetylase 5 (5 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Galc Galactocerebrosidase (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HD1 Histone deacetylase (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Micrococcus luteus (7463 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
unidentified influenza virus (265 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
L1210 (27553 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
mdlA Mandelate racemase (27 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasma (328 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
bla-imp13 IMP-13 (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PA Polymerase acidic protein (806 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
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.

32 results found

Lot NumberCertificate TypeDateItem
E2615502Certificate of AnalysisApr 27, 2026 B152659
E2615483Certificate of AnalysisApr 27, 2026 B152659
E2615500Certificate of AnalysisApr 27, 2026 B152659
E2615501Certificate of AnalysisApr 27, 2026 B152659
I2523164Certificate of AnalysisSep 11, 2025 B152659
I2523170Certificate of AnalysisSep 11, 2025 B152659
I2523173Certificate of AnalysisSep 11, 2025 B152659
I2523176Certificate of AnalysisSep 11, 2025 B152659
I2523179Certificate of AnalysisSep 11, 2025 B152659
L2106127Certificate of AnalysisSep 09, 2025 B152659
D2524145Certificate of AnalysisApr 10, 2025 B152659
D2524144Certificate of AnalysisApr 10, 2025 B152659
D2524143Certificate of AnalysisApr 10, 2025 B152659
D2524142Certificate of AnalysisApr 10, 2025 B152659
H2408187Certificate of AnalysisJul 26, 2024 B152659
H2408188Certificate of AnalysisJul 26, 2024 B152659
H2408225Certificate of AnalysisJul 26, 2024 B152659
D2016118Certificate of AnalysisFeb 05, 2024 B152659
L2306245Certificate of AnalysisNov 25, 2023 B152659
L2306246Certificate of AnalysisNov 25, 2023 B152659
L2306247Certificate of AnalysisNov 25, 2023 B152659
L2306248Certificate of AnalysisNov 25, 2023 B152659
L2206272Certificate of AnalysisOct 25, 2022 B152659
L2206274Certificate of AnalysisOct 25, 2022 B152659
L2206277Certificate of AnalysisOct 25, 2022 B152659
L2206280Certificate of AnalysisOct 25, 2022 B152659
L2206281Certificate of AnalysisOct 25, 2022 B152659
F2228158Certificate of AnalysisJul 01, 2022 B152659
F2228155Certificate of AnalysisJul 01, 2022 B152659
F2228152Certificate of AnalysisJul 01, 2022 B152659
F2228144Certificate of AnalysisJul 01, 2022 B152659
C2203064Certificate of AnalysisMar 15, 2022 B152659

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Chemical and Physical Properties
SolubilitySoluble in alcohol. Slightly soluble in ether. Insoluble in benzene.
SensitivityAir sensitive
Melt Point(°C)124 °C(dec.)
Molecular Weight137.140 g/mol
XLogP30.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass137.048 Da
Monoisotopic Mass137.048 Da
Topological Polar Surface Area49.300 Ų
Heavy Atom Count10
Formal Charge0
Complexity119.000
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
Documents & Articles
Citations of This Product
References
1. Kuixin Cui, Shengming Jin, Nan Duan.  (2023)  Insights into the adsorption mechanism of benzohydroxamic acid in the flotation of rhodochrosite with Pb2+ activation.  POWDER TECHNOLOGY,      [PMID:] [10.1016/j.powtec.2023.118705]
2. Mengke Li, Zhiguo He, Hui Zhong, Wei Sun, Mingqiang Ye, Yihui Zhou.  (2022)  A novel multi-components hierarchical porous composite prepared from solid wastes for benzohydroxamic acid degradation.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:36347098] [10.1016/j.jcis.2022.10.124]
3. Ruolin Wang, Wenjuan Sun, Haisheng Han, Wei Sun, Zhao Wei, Jian Peng.  (2022)  Al-caustic starch coordination compounds: A new depressant for fine calcite.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2022.129268]
4. Xinyang Yu, Ruirui Zhang, Yuhui Zeng, Chen Cheng, Zhiqiang Huang, Jinliang Wang, Guichun He, Haolin Wang.  (2021)  The effect and mechanism of cinnamic hydroxamic acid as a collector in flotation separation of malachite and calcite.  MINERALS ENGINEERING,      [PMID:] [10.1016/j.mineng.2021.106847]
5. Zheyu Huang, Jingzhong Kuang, Luping Zhu, Weiquan Yuan, Zhilei Zou.  (2021)  Effect of ultrasonication on the separation kinetics of scheelite and calcite.  MINERALS ENGINEERING,      [PMID:] [10.1016/j.mineng.2020.106762]
6. Shiman Zhu, Liuyi Ren, Shenxu Bao, Yimin Zhang, Bo Chen.  (2024)  Effect of different particle size fractions on flotation separation of fine rutile from garnet.  ADVANCED POWDER TECHNOLOGY,      [PMID:] [10.1016/j.apt.2024.104396]
7. Yuqi Miao, Jianyong He, Xinran Zhu, Guangli Zhu, Shaohang Cao, Guixia Fan, Guosheng Li, Yijun Cao.  (2024)  Hardness of surface hydroxyls and its pivotal role in the flotation of cassiterite from quartz via lead ions activation.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.127565]
8. Longfu Dai, Jian Liu, Deqiang Luo, Runpeng Liao, Da Li.  (2024)  Investigation of the adsorption mechanism of an eco-friendly surfactant LMAC on rutile surface: A novel insight.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.129484]
9. Rui Li, Yanhai Shao, Jinhui Li, Chenjie Liu, Hongqin Chen, Xiao Meng, Xinru Jia.  (2024)  Mechanism of Efficient Smithsonite Flotation with a Ternary Composite Collector Under Sulfur-Free Conditions.  MOLECULES,  29  (24): (6014).  [PMID:39770102] [10.3390/molecules29246014]
10. Jiang Hanxiang, Qi Jiangfeng, Wang Jiwen, Chen Jiaqin, Feng Dong, Yang Junbiao, Liu Xinna, Liu Mengqun, Zhou Xvzhe, An Zhilong, Lu Yuanyuan, Ge Chun, Wang Ying.  (2025)  Terramide A: a novel ironophore targeting Acinetobacter baumannii with mechanistic insights into bacterial iron deprivation.  JOURNAL OF ANTIBIOTICS,      [PMID:40164737] [10.1038/s41429-025-00816-9]
11. Zheyu Huang, Jingzhong Kuang, Tingsheng Qiu, Mingming Yu.  (2025)  Effect of metal phenolic networks constructed via tannic acid coordination with Fe³ ⁺ on scheelite/calcite flotation selectivity.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2025.138240]
12. Jiaqiao Yuan, Xiang Gong, Hongyu Lu, Wei Jiang, Hao Lai, Shuming Wen, Shaojun Bai, Dandan Wu.  (2025)  Adsorption mechanism of a novel collector (2-ethylhexyl) phosphonic acid mono-2-ethylhexyl ester for selective flotation separation of ilmenite from titanaugite.  MINERALS ENGINEERING,      [PMID:] [10.1016/j.mineng.2025.109340]
13. Yuanbo Zhang, Hua Chen, Zijian Su, Zhidong Jiang, Kaiao Shen.  (2025)  Adsorption mechanisms of benzohydroxamic acid and sodium oleate on calcium stannate: Combined experimental and DFT study for enhancing flotation recovery.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2025.117059]
14. Jieyi Wang, Hairong Shen, Mengke Li, Chenquan Ni, Hui Zhong, Zhiguo He.  (2025)  Sulfurization-derived Fe3S4 in copper tailings as a peroxymonosulfate activator for efficient salicylhydroxamic acid degradation.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.170913]
15. Chang Shen, Xiong Tong, Jing Qi, Xian Xie, Ruiqi Xie.  (2025)  Selective separation of cassiterite from quartz using (2-ethylhexyl) phosphonic acid mono-2-ethylhexyl ester.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2025.165398]
16. Yiping Wang, Tao Liu, Yimin Zhang, Nannan Xue, Pengcheng Hu.  (2025)  Enhanced pH adaptability in vanadium solvent extraction: Synergistic coordination of octanohydroxamate and D2EHPA for efficient extraction at low pH.  Journal of Environmental Chemical Engineering,  14  (1): (120757).  [PMID:] [10.1016/j.jece.2025.120757]
17. Zheyu Huang, Jingzhong Kuang, Tingsheng Qiu, Mingming Yu.  (2026)  Mechanisms of Ligand Structures of Fe-Salicylic Acid and Fe-Gallic Acid Colloidal Complexes Regulating the Flotation Behavior of Scheelite with Calcite.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2026.139507]
18. Jieliang Wang, Xiaobin Zhong, Wenqiang Zhu, Jing Lv, Qin Zhang, Zhiyong Gao, Zhao Cao.  (2026)  Unraveling interfacial interaction mechanism: Towards selective depression of ankerite by carboxymethyl cellulose in columbite flotation.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,      [PMID:] [10.1016/j.colsurfa.2026.139804]
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