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1,2,4,5-Benzenetetramine tetrahydrochloride - ≥97%, high purity , CAS No.4506-66-5

En stock
Item Number
B303744
Articles du produit groupé
SKU Taille
Disponibilité
Prix Qté
B303744-1g
1g
5
59,90$US
B303744-5g
5g
4
199,90$US
B303744-25g
25g
1
699,90$US

FAK autophosphorylation inhibitor. 1 ml water soluble pack.

Description générale

Synonymes Y15 | 1,2,4,5-Tetraaminobenzene tetrahydrochloride | FAK Inhibitor 14 | Benzene-1,2,4,5-tetraamine tetrahydrochloride
Spécifications et pureté Moligand™, ≥97%
Mécanismes biochimiques et physiologiques Selective focal adhesion kinase (FAK) autophosphorylation inhibitor (IC 50 = 1 μM). No significant activity at other kinases including EGFR, PDGFR and IGF-RI. Increases cell detachment and inhibits cell adhesion in cancer cells. Anticancer agent.
Température de stockage Room temperature
Expédié en Normal
Grade Moligand™
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

1,2,4,5-Benzenetetraminetetrahydrochloride is widely used as a novel source of carbon and nitrogen insynthesizing benzimidazole-linked polymers and carbon dot nanomaterials.

Application:

1,2,4,5-Benzenetetramine tetrahydrochloride can be used as a precursor in the synthesis of:
A pyrene-based benzimidazole-linked polymer by the co-condensation with 1,3,6,8-tetrakis(4-formylphenyl)pyrene in dimethylformamide.
Triazine-based benzimidazole-linked polymers for highly selective CO2 capture.
Nitrogen-doped carbon dots (NCDs) by simple hydrothermal method, applicable as a highly selective fluorescent probe for sensing Mg2+ ions in an aqueous solution.
Red-emitting carbon dots via the solvothermal method.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Classe Benzene and substituted derivatives
Subclass Aniline and substituted anilines
Intermediate Tree Nodes Not available
Direct Parent Aniline and substituted anilines
Alternative Parents Primary amines  Organopnictogen compounds  Hydrochlorides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Aniline or substituted anilines - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary amine - Organonitrogen compound - Amine - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as aniline and substituted anilines. These are organic compounds containing an aminobenzene moiety.
External Descriptors Not available

Noms et identifiants

Pubchem Sid 488185549
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488185549
IUPAC Name benzene-1,2,4,5-tetramine;tetrahydrochloride
INCHI InChI=1S/C6H10N4.4ClH/c7-3-1-4(8)6(10)2-5(3)9;;;;/h1-2H,7-10H2;4*1H
InChIKey BZDGCIJWPWHAOF-UHFFFAOYSA-N
Smiles C1=C(C(=CC(=C1N)N)N)N.Cl.Cl.Cl.Cl
Isomères SMILES C1=C(C(=CC(=C1N)N)N)N.Cl.Cl.Cl.Cl
PubChem CID 78260
Poids moléculaire 284.02

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

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.

13 results found

Lot Number Certificate Type Date Article
A2514532 Certificate of Analysis Jan 06, 2025 B303744
A2514548 Certificate of Analysis Jan 06, 2025 B303744
E2406321 Certificate of Analysis Mar 15, 2024 B303744
C2412022 Certificate of Analysis Mar 18, 2023 B303744
D2327078 Certificate of Analysis Mar 18, 2023 B303744
D2327079 Certificate of Analysis Mar 18, 2023 B303744
B2418139 Certificate of Analysis Mar 18, 2023 B303744
D2327082 Certificate of Analysis Mar 18, 2023 B303744
D2327083 Certificate of Analysis Mar 18, 2023 B303744
D2327077 Certificate of Analysis Mar 18, 2023 B303744
D2327080 Certificate of Analysis Mar 18, 2023 B303744
K2322084 Certificate of Analysis Mar 18, 2023 B303744
D2423068 Certificate of Analysis Mar 18, 2023 B303744

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Propriétés chimiques et physiques

Sensibilité Moisture sensitive.
Poids moléculaire 284.000 g/mol
XLogP3
Hydrogen Bond Donor Count 8
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 0
Exact Mass 283.994 Da
Monoisotopic Mass 281.997 Da
Topological Polar Surface Area 104.000 Ų
Heavy Atom Count 14
Formal Charge 0
Complexity 90.300
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 5

Citations of This Product

1. Xiang Gang, Li Wenzhuo, Nong Qiuxiang, Zhang Cuizhong, Zhang Zhengfa, Lian Huan, Peng Jinyun, Jiang Yufen, Tan Yiqiu, Sun Jing.  (2023)  Quinoxaline core-conjugated microporous polymer coating for highly sensitive solid-phase microextraction of phthalate esters in liquid food samples.  Journal of Food Measurement and Characterization,  17  (6): (6168-6179). 
2. Kai Niu, Yuying Zhang, Jiping Chen, Xianbo Lu.  (2022)  2D Conductive Covalent Organic Frameworks with Abundant Carbonyl Groups for Electrochemical Sensing.  ACS Sensors,  (11): (3551–3559). 
3. Wu Di, Song Qingzhi, Cui Deliang, Li Yanlu, Wang Qilong, Yu Haohai, Lian Gang.  (2025)  Aromatic polyamine-grafted and nitrogen-doped graphene anodes boosting surface-dominated sodium storage.  Advanced Composites and Hybrid Materials,  (2): (1-12). 
4. Zhang Zhen, Xing Zhenyu, Luo Xianglin, Cheng Chong, Liu Xikui.  (2025)  Densely populated macrocyclic dicobalt sites in ladder polymers for low-overpotential oxygen reduction catalysis.  Nature Communications,  16  (1): (1-12). 
5. Yahui Zhu, Xiaohua Ma, Wenjie Lai, Zengxiang Tang, Weiming Xiao, Rong Zeng, Shunmin Ding, Chao Chen.  (2025)  Investigation of the catalytic mechanism of targeted adsorption and selective hydrogenation based on d-π conjugated derivatives.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,  686  (990). 

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