Urea-¹⁵N₂ - ≥5 atom% 15N,≥99% , CAS No.2067-80-3

CAS: 2067-80-3 Cat. No.: U432298 Formula: 15NH2CO15NH2 Peso molecolare: 62.04 Numero EC: 629-503-9
Disponibile su ordine
GRADE & PURITY ≥5 atom% 15N,≥99%
Synonyms
J-013518 | MS-22715 | AKOS015913372 | bis(15N)(azanyl)methanone | Urea-15N2 | HY-Y0271S | Urea N-15 | JD9TPJ3YLS | Urea-15N2, >=10 atom % 15N, >=96% (CP) | Urea-15N2, 98 atom % 15N, 99% (CP) | UNII-JD9TPJ3YLS | Urea-15N2, 2 atom % 15N, 99% (CP) | Urea-15N
Storage
Room temperature
Size
Germania (EU)
USA*
Price
Qty
50g
U432298-50g
Su ordinazione · 8–12 settimane

1.583,54€

1.848,20€
Salva 264,66 € (14.32%)
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Why this grade

≥5 atom% 15N,≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Check lot-specific COA for exact specifications.

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Quality documents

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

📚

Literature proof

Cited in 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinonimi
J-013518 | MS-22715 | AKOS015913372 | bis(15N)(azanyl)methanone | Urea-15N2 | HY-Y0271S | Urea N-15 | JD9TPJ3YLS | Urea-15N2, >=10 atom % 15N, >=96% (CP) | Urea-15N2, 98 atom % 15N, 99% (CP) | UNII-JD9TPJ3YLS | Urea-15N2, 2 atom % 15N, 99% (CP) | Urea-15N
Specifiche e purezza
≥5 atom% 15N,≥99%
Condizioni di conservazione di stoccaggio
Room temperature
Purezza
≥5 atom% 15N,≥99%
Nomi e identificatori
Sorrisi canoniciC(=O)(N)N
IUPAC Namebis(15N)(azanyl)methanone
InChIKeyXSQUKJJJFZCRTK-SUEIGJEOSA-N
INCHI1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)/i2+1,3+1
Isomeri SMILES C(=O)([15NH2])[15NH2]
WGK Germania 3
CAS alternativo 57-13-6(Unlabeled)
Peso molecolare 62.04

Documentazione

📋 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
SuperclassOrganic acids and derivatives
ClasseOrganic carbonic acids and derivatives
SubclassUreas
Intermediate Tree Nodes Not available
Direct ParentUreas
Alternative Parents Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Urea - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as ureas. These are compounds containing two amine groups joined by a carbonyl (C=O) functional group.
External Descriptors Not available
Struttura 3D
Modello di struttura chimica interattiva





Certificati (CoA, COO, BSE/TSE e tabella di analisi)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Proprietà chimiche e fisiche
Punto di fusione (°C)132-135°C
Peso molecolare62.042 g/mol
XLogP3-1.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass62.0264 Da
Monoisotopic Mass62.0264 Da
Topological Polar Surface Area69.100 Ų
Heavy Atom Count4
Formal Charge0
Complexity29.000
Isotope Atom Count2
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
Domande frequenti e articoli
Citations of This Product
Riferimenti
1. Yini Mao, Yong Jiang, Qiao Gou, Shengmei Lv, Zuyou Song, Yimin Jiang, Wenbin Wang, Ming Li, Lirong Zheng, Wei Su, Rongxing He.  (2023)  Indium-activated bismuth-based catalysts for efficient electrocatalytic synthesis of urea.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2023.123189]
2. Zhiwei Liang, Yuguo Xia, Guiming Ba, Haiping Li, Quanhua Deng, Wanguo Hou.  (2019)  Sb-doped polymeric carbon nitride with charge-capture centers for efficient charge separation and photocatalytic performance in H2 evolution and environmental remediation.  Catalysis Science & Technology,  (23): (6627-6637).  [PMID:] [10.1039/C9CY01862J]
3. Shi-Peng Chen, Dan-Yang Zhao, Jin-Long Zhu, Jing Wang, Gan-Ji Zhong, Hua-Dong Huang, Zhong-Ming Li.  (2024)  Hydrogen bond producers in powerful protic ionic liquids for enhancing dissolution of natural cellulose.  SusMat,      [PMID:] [10.1002/sus2.238]
4. Qizhu Qian, Qilong Liu, Mengxiang Wang, Jingjing Yang, Huiyi Li, Wei Bai, Wentao Wang, Changzheng Wu, Chong Xiao, Yi Xie.  (2025)  Dual-site cooperation for synergistic optimization of the band structure and spin state to facilitate C–N coupling reaction.  PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,  122  (43): (e2508077122).  [PMID:41118215] [10.1073/pnas.2508077122]
5. Jiaxin Du, Yunshuo Wu, Siyu Fang, Daliang Xu, Min Liu, Heng Liang, Zhongbiao Wu, Gaoqing Max Lu, Xuanhao Wu.  (2025)  Nano-confinement engineering boosts C–N coupling for urea electrosynthesis.  Nature Communications,      [PMID:41453889] [10.1038/s41467-025-67741-1]
6. Cenwei Liu, Jing Ye, Yi Lin, Bangwei Zhang, Weixi Shu, Yixiang Wang.  (2026)  Low-dose biochar and nitrogen fertilizer reduces nitrogen loss in acidic tea soils.  iScience,      [PMID:41847108] [10.1016/j.isci.2026.115194]
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