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Basic Description
| Synonyms | 4-03-00-00177 (Beilstein Handbook Reference) | SDCCGSBI-0051066.P002 | BRN 0506319 | 1-azanylurea | BBL012207 | EINECS 200-339-6 | Lopac-S-2201 | D95915 | Carbamoylhydrazine | HYDRAZINECARBOXAMIDE | Q417535 | CHEBI:28306 | Semicarbazide, 6 wt. % (on silic |
|---|---|
| Specifications & Purity | 6 wt. % (on silica gel) |
| Storage Temp | Room temperature |
| Shipped In | Normal |
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
- Superclass Organic acids and derivatives
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Carboximidic acids and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Carboximidic acids and derivatives |
| Alternative Parents | Organopnictogen compounds Organooxygen compounds Imines Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Carboximidic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Imine - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as carboximidic acids and derivatives. These are compounds containing a carboximidic group, with the general formula R-C(=NR1)OR2. |
| External Descriptors | a carboxamide |
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Associated Targets(Human)
MAOB
Tclin
Amine oxidase [flavin-containing] B (1 Activities)
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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CHRM1
Tclin
Muscarinic acetylcholine receptor M1 (12690 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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TSHR
Tclin
Thyroid stimulating hormone receptor (29986 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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MAOA
Tclin
Monoamine oxidase A (11911 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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MAOB
Tclin
Monoamine oxidase B (8835 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ARSA
Tbio
Cerebroside-sulfatase (655 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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CYP2D6
Tclin
Cytochrome P450 2D6 (33882 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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NFKB1
Tclin
Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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CYP1A2
Tchem
Cytochrome P450 1A2 (26471 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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CYP2C9
Tchem
Cytochrome P450 2C9 (32119 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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CYP2C19
Tchem
Cytochrome P450 2C19 (29246 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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CYP3A4
Tclin
Cytochrome P450 3A4 (53859 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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EHMT2
Tchem
Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Associated Targets(non-human)
Mus musculus (284745 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Rattus norvegicus (775804 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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L1210 (27553 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Txnrd1
Thioredoxin reductase 1, cytoplasmic (45279 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Names and Identifiers
| Pubchem Sid | 488179884 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488179884 |
| IUPAC Name | aminourea |
| INCHI | InChI=1S/CH5N3O/c2-1(5)4-3/h3H2,(H3,2,4,5) |
| InChIKey | DUIOPKIIICUYRZ-UHFFFAOYSA-N |
| Smiles | C(=O)(N)NN |
| Isomeric SMILES | C(=O)(N)NN |
| WGK Germany | 3 |
| PubChem CID | 5196 |
| Molecular Weight | 75.07 |
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.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 I2212347 |
Certificate of Analysis | Jun 10, 2025 | S171063 |
| I2212348 |
Certificate of Analysis | Jun 10, 2025 | S171063 |
| E2225197 |
Certificate of Analysis | Mar 04, 2025 | S171063 |
| E2225219 |
Certificate of Analysis | Mar 04, 2025 | S171063 |
| G2116324 |
Certificate of Analysis | Apr 07, 2024 | S171063 |
| G2305829 |
Certificate of Analysis | Feb 17, 2023 | S171063 |
| G23051291 |
Certificate of Analysis | Feb 17, 2023 | S171063 |
| G2305858 |
Certificate of Analysis | Feb 17, 2023 | S171063 |
| G23051289 |
Certificate of Analysis | Feb 17, 2023 | S171063 |
Chemical and Physical Properties
| Molecular Weight | 75.070 g/mol |
|---|---|
| XLogP3 | -1.800 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 75.0433 Da |
| Monoisotopic Mass | 75.0433 Da |
| Topological Polar Surface Area | 81.100 Ų |
| Heavy Atom Count | 5 |
| Formal Charge | 0 |
| Complexity | 42.200 |
| 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 |
Citations of This Product
| 1. Li Fu, Zerui Liu, Pengjie Dong, Yingshu Guo. (2023) Electrochemiluminescence Mechanistic Insights of CuInS2/ZnS Nanocrystals with Hydrazine Compounds as Co-reactants. Journal of Physical Chemistry C, 127 (46): (22827–22832). |
| 2. Lingqiao Zhang, Siqi Wei, Limei Zhang, Xinghang Yin, Rui Yang. (2024) A novel type of fluorescence modulation mechanism of carbon dots derived from the competition of photoinduced electron transfer and fluorescence. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 304 (123276). |
| 3. Xu Wen, Xueling Yan, Xiaoling Zheng, Qiming Kou, Lulan Yang, Jiaming Tang, Xingyue Chen, Yong Xie, Tao Le. (2023) Selection and truncation of aptamers as fluorescence sensing platforms for selective and sensitive detection of nitrofurazone. ANALYTICA CHIMICA ACTA, 1252 (341044). |
| 4. Lihong Xing, Weihong Sun, Xiaojie Sun, Jixing Peng, Zhaoxin Li, Panpan Zhu, Xuying Zheng. (2021) Semicarbazide Accumulation, Distribution and Chemical Forms in Scallop (Chlamys farreri) after Seawater Exposure. Animals, 11 (6): (1500). |
| 5. Xiaoling Zheng, Shuang Jiang, Yueyang Ren, Sixian Wang, Yong Xie, Tao Le. (2024) High-efficient selection of aptamers by magnetic cross-linking precipitation and development of aptasensor for 1-aminohydantoin detection. LWT-FOOD SCIENCE AND TECHNOLOGY, 199 (116128). |
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