Oxamide - ≥98% , CAS No.471-46-5

CAS: 471-46-5 Cat. No.: O113868 Molecular Weight: 88.07 Beilstein Registry Number: 1743262 EC Number: 207-442-5

GRADE & PURITY ≥98%

Synonyms

ETHANEDIOIC ACID DIAMIDE | Formimidic acid, 1-carbamoyl- | WLN: ZVVZ | Oxamimidic acid | OXAMIDE | Amid kyseliny stavelove [Czech] | Oxamicacid amide | Amid kyseliny stavelove | D70377 | MFCD00008007 | FT-0632177 | NCI60_002253 | Oxalic acid diamide | AI3

Storage

Room temperature

Shipped In

Normal

Overview

Oxamide can be used:

· As a precursor for the synthesis of ligands such as bis(benzimidazole) and Schiff base ligands formed by condensation with furfural.

· Carbon nitride (g-C3N4) nanotubes by self-assembly polymerization with urea.

· As a bridging ligand for the synthesis of binuclear IrIII complex [Ir2(μ2-oxamidato-N,N′,O,O′)(ptpy)4], ptpy = 2-(p-tolyl)pyridinato

Specifications

Synonyms

ETHANEDIOIC ACID DIAMIDE | Formimidic acid, 1-carbamoyl- | WLN: ZVVZ | Oxamimidic acid | OXAMIDE | Amid kyseliny stavelove [Czech] | Oxamicacid amide | Amid kyseliny stavelove | D70377 | MFCD00008007 | FT-0632177 | NCI60_002253 | Oxalic acid diamide | AI3

Specifications & Purity

≥98%

Storage

Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488181082
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181082
• Canonical Smiles: C(=O)(C(=O)N)N
• IUPAC Name: oxamide
• InChIKey: YIKSCQDJHCMVMK-UHFFFAOYSA-N
• INCHI: 1S/C2H4N2O2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)
• Isomeric SMILES: C(=O)(C(=O)N)N
• WGK Germany: 3
• RTECS: RO4900000
• Molecular Weight: 88.07
• Beilstein: 1743262
• Reaxy-Rn: 1743262
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1743262&ln=

Associated Targets(Human)

A498 (42825 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHN (49357 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CCRF-CEM (65223 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

COLO 205 (50209 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DLD-1 (17511 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

DMS-273 (14108 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HL-60 (67320 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

K562 (73714 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KM12 (47707 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

M14 (47487 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MOLT-4 (49676 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OVCAR-3 (48710 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OVCAR-5 (45555 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

OVCAR-8 (47708 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RPMI-8226 (44974 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXF 393 (41971 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SF-295 (48000 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SK-MEL-2 (46422 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SK-MEL-28 (48833 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SK-MEL-5 (47095 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SK-OV-3 (52876 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SN12C (47755 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SNB-19 (46794 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SNB-78 (14240 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TK-10 (45540 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

U-251 (51189 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UACC-257 (46019 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UACC-62 (47335 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UO-31 (46270 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

XF498 (12972 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

786-0 (47912 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

A549 (127892 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

EKVX (44102 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NCI-H322M (45589 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HCC 2998 (41480 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HCT-116 (91556 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HOP-18 (11577 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HOP-92 (41141 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NCI-H460 (60772 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SF-268 (49410 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

KM-20L2 (14967 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LOX IMVI (44321 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

HOP-62 (47048 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

LXFL 529 (14112 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

M19-MEL (15326 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Malme-3M (44254 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NCI-H23 (49055 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NCI-H522 (44358 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SF-539 (44845 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SR (39847 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in ethanol, slightly soluble in water and insoluble in diethyl ether.
• Melt Point(°C): 491°C
• Molecular Weight: 88.070 g/mol
• XLogP3: -1.600
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 88.0273 Da
• Monoisotopic Mass: 88.0273 Da
• Topological Polar Surface Area: 86.200 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 75.500
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

References

1. Jiayi Li, Ying Huang, Minhua Su, Yuying Xie, Diyun Chen.  (2021)  Dual light-driven p-ZnFe2O4/n-TiO2 catalyst: Benzene-breaking reaction for malachite green.  ENVIRONMENTAL RESEARCH,      [PMID:34597665] [10.1016/j.envres.2021.112081]

2. Guoqiang Zhang, Wei Huang, Yangsen Xu, Yongliang Li, Chuanxin He, Xiangzhong Ren, Peixin Zhang, Hongwei Mi.  (2023)  Suppressing Defects-Induced Non-Radiative Recombination for Activating the Near-Infrared Photoactivity of Red Polymeric Carbon Nitride.  ADVANCED FUNCTIONAL MATERIALS,  33  (52): (2305935).  [PMID:] [10.1002/adfm.202305935]

3. Ming Chen, Linyang Li, Lanlan Zhong, Chuanbao Xiao, Nianbing Zhong, Quanhua Xie, Dengjie Zhong, Yunlan Xu, Haixing Chang.  (2023)  Complete removal of 4-fluorophenol using a novel optical fiber photocatalysis–biodegradation–ion-adsorption system.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.142631]

4. Xue Bai, Jiangna Xing, Xin Huang, Shiyu Sun, Na Wang, Ting Wang, Hongxun Hao.  (2025)  3D spongy porous g-C3N4 material synthesized by supramolecular self-assembly for efficient degradation of tetracycline.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.162782]

5. Nanzhi Zheng, Yuchen Yang, Wenhao Huang, Jianting Zhang, Guohua Chen.  (2025)  Boric Acid-Catalyzed Synthesis: A scalable strategy for High-Yield and Tunable red fluorescent carbon dots.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:40523329] [10.1016/j.saa.2025.126562]

6. Hao Zeng, Xiangbing Zou, Shuo Yang, Sizhe Tang, Shanshan Luo, Meiyue Cheng, Haiping Xu, Yujie Song, Ming Liu, Yang Liu, Ming Yang, Bing Li.  (2026)  Functional group engineering for boosting catalytic activity: high turnover frequency in electrocatalytic CO2 reduction and Zn-CO2 batteries.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:41621356] [10.1016/j.jcis.2026.139983]