Hydrazine solution - 1.0 M in THF , CAS No.302-01-2

CAS: 302-01-2 Cat. No.: H432566 Peso molecular: 32.046 Número EC: 206-114-9

GRADE & PURITY 1.0 M in THF

Synonyms

27RFH0GB4R | Amerzine (Salt/Mix) | Hydrazine (hydrazine sulphate) | STL281862 | Diamidogen | HYDRAZINE AQUEOUS SOLUTION | ISONIAZID IMPURITY E [EP IMPURITY] | Scav-Ox II (Salt/Mix) | (anhydrous) | Hydrazyna [Polish] | RCRA waste no. U133 | UN3293 | Zerox

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

Descripción general

Hydrazine promotes the cation exchange reaction for fast doping Cu ions into ZnSe nanocrystals.

Application

Hydrazine solution may be employed for the following studies: As reducing agent for the reduction of the first row (3.Flammable liquidd) transition metal complexes in aqueous solution. Preparation of nanoscale reduced metal oxides such as VO 2 (B), Cr 2 O 3.Flammable liquid . As fuel for the direct hydrazine fuel cell (DHFC). As reducing agent for the synthesis of metallic monodisperse copper nanoparticles.

Specifications

Sinónimos

27RFH0GB4R | Amerzine (Salt/Mix) | Hydrazine (hydrazine sulphate) | STL281862 | Diamidogen | HYDRAZINE AQUEOUS SOLUTION | ISONIAZID IMPURITY E [EP IMPURITY] | Scav-Ox II (Salt/Mix) | (anhydrous) | Hydrazyna [Polish] | RCRA waste no. U133 | UN3293 | Zerox

Especificaciones y pureza

1.0 M in THF

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

FedEx DG Service

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

• Sonrisas canónicas: NN
• IUPAC Name: hydrazine
• InChIKey: OAKJQQAXSVQMHS-UHFFFAOYSA-N
• INCHI: 1S/H4N2/c1-2/h1-2H2
• Isómeros SMILES: NN
• Número ONU: 3293
• Grupo de embalaje: III
• Peso molecular: 32.046

Taxonomic Classification

Taxonomy Tree

• Kingdom Inorganic compounds
  • Superclass Homogeneous non-metal compounds
    • Clase Homogeneous other non-metal compounds

• Kingdom: Inorganic compounds
• Superclass: Homogeneous non-metal compounds
• Clase: Homogeneous other non-metal compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Homogeneous other non-metal compounds
• Alternative Parents: Hydrazines and derivatives
• Molecular Framework: Not available
• Substituents: Homogeneous other non metal - Hydrazine derivative
• Descripción: This compound belongs to the class of inorganic compounds known as homogeneous other non-metal compounds. These are inorganic non-metallic compounds in which the largest atom belongs to the class of 'other non-metals'.
• External Descriptors: a small molecule

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)

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EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)

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CA2 Tclin Carbonic anhydrase II (17698 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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HMGCR Tclin HMG-CoA reductase (2475 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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INSR Tclin Insulin receptor (5558 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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ACE Tclin Angiotensin-converting enzyme (1423 Activities)

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DRD2 Tclin Dopamine D2 receptor (23596 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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DRD4 Tchem Dopamine D4 receptor (7907 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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HRH2 Tclin Histamine H2 receptor (5428 Activities)

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ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)

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HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)

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HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)

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HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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CALCR Tclin Calcitonin receptor (2215 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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HRH1 Tclin Histamine H1 receptor (7573 Activities)

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ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)

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OPRD1 Tclin Delta opioid receptor (15096 Activities)

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OPRK1 Tclin Kappa opioid receptor (16155 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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KCNH2 Tclin HERG (29587 Activities)

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HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)

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ESR2 Tclin Estrogen receptor beta (9272 Activities)

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CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)

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ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)

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CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)

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CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)

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ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)

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Objetivos asociados (no humanos)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)

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Mc4r Melanocortin receptor 4 (1205 Activities)

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Ltc4s Leukotriene C4 synthase (1 Activities)

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Sigmar1 Sigma opioid receptor (160 Activities)

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Npy1r Neuropeptide Y receptor type 1 (8 Activities)

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Cckar Cholecystokinin A receptor (90 Activities)

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Nos2 Nitric oxide synthase, inducible (3573 Activities)

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Mapk1 MAP kinase ERK2 (650 Activities)

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Mmp9 Matrix metalloproteinase 9 (38 Activities)

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Rattus norvegicus (775804 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Peso molecular: 32.046 g/mol
• XLogP3: -1.500
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 32.0374 Da
• Monoisotopic Mass: 32.0374 Da
• Topological Polar Surface Area: 52.000 Ų
• Heavy Atom Count: 2
• Formal Charge: 0
• Complexity: 0.000
• 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

Referencias

1. J.Y. Yong, R.Y. Xie, Q. Huang, X.J. Zhang, B. Li, P.F. Xie, C.F. Wu, L. Jiang.  (2023)  Diamine-appended metal-organic framework for carbon capture from wet flue gas: Characteristics and mechanism.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2023.125018]

2. Shengji Xia, Muzi Ni, Tongren Zhu, Yu Zhao, Nana Li.  (2015)  Ultrathin graphene oxide nanosheet membranes with various d-spacing assembled using the pressure-assisted filtration method for removing natural organic matter.  DESALINATION,      [PMID:] [10.1016/j.desal.2015.06.005]

3. Wei Zheng, Minyu Li, Hongmei Chen, Fuyin Xie, Zequn Yang, Lijian Leng, Jianping Yang, Wenqi Qu, Hailong Li.  (2025)  Synthesis of Selenized Metal–Organic Framework Hollow Cage under Ambient Condition for Clean Energy Applications.  ACS Applied Materials & Interfaces,      [PMID:39962754] [10.1021/acsami.4c17913]

4. Xue-qi Zhang, Rui Ding, Jing Lv, Yu-chen Zhang, An-lan Ji, Jie Fu, Xiao Lv, Sheng-ying Yang, Lan Yao, Xuan Liang, Jie Liu, Hai-bin Yu.  (2023)  The novel damage-reporting and self-healing coatings prepared by electrospinning technology based on AIE agents and photothermal shape memory polymer.  JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY,      [PMID:] [10.1016/j.jiec.2023.12.050]

5. Jiaran Zhang, Zeyu Xu, Ce Shi, Xinting Yang.  (2021)  A Fluorescence Method Based on N, S-Doped Carbon Dots for Detection of Ammonia in Aquaculture Water and Freshness of Fish.  Sustainability,  13  (15): (8255).  [PMID:] [10.3390/su13158255]

6. Xingyu Zhao, Minmin Chen, Hualin Wang, Li Xia, Min Guo, Suwei Jiang, Qian Wang, Xingjiang Li, Xuefei Yang.  (2020)  Synergistic antibacterial activity of streptomycin sulfate loaded PEG-MoS2/rGO nanoflakes assisted with near-infrared.  Materials Science & Engineering C-Materials for Biological Applications,      [PMID:32806251] [10.1016/j.msec.2020.111221]

7. Tang Lina, Li Yutao, Xie Hui, Shu Qing, Yang Fan, Liu Yan-ling, Liang Fengxia, Wang Hua, Huang Weihua, Zhang Guo-Jun.  (2017)  A sensitive acupuncture needle microsensor for real-time monitoring of nitric oxide in acupoints of rats.  Scientific Reports,  7  (1): (1-10).  [PMID:28744003] [10.1038/s41598-017-06657-3]

8. Binghu Wang, Saihu Pan, Yong Qin, Wensheng Tan, Yongxin Tao, Kaijian Li, Yong Kong.  (2017)  Synthesis of efficient electrocatalyst for oxygen reduction reaction by using poly(m-phenylenediamine) as the interlayer spacer and the sources of N-doped carbon and MnO.  SYNTHETIC METALS,      [PMID:] [10.1016/j.synthmet.2016.12.028]

9. Hong-Lei Shuai, Ke-Jing Huang, Ling-Li Xing, Ying-Xu Chen.  (2016)  Ultrasensitive electrochemical sensing platform for microRNA based on tungsten oxide-graphene composites coupling with catalyzed hairpin assembly target recycling and enzyme signal amplification.  BIOSENSORS & BIOELECTRONICS,      [PMID:27392235] [10.1016/j.bios.2016.06.057]

10. Juanjuan Gao, Shupeng Zhang, Maoxiang Liu, Yu Tai, Xin Song, Yueyue Qian, Haiou Song.  (2015)  Synergistic combination of cyclodextrin edge-functionalized graphene and multiwall carbon nanotubes as conductive bridges toward enhanced sensing response of supramolecular recognition.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2015.11.073]

11. Ruiling Sun, Yong Wang, Yongnian Ni, Serge Kokot.  (2013)  Spectrophotometric analysis of phenols, which involves a hemin–graphene hybrid nanoparticles with peroxidase-like activity.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:24374565] [10.1016/j.jhazmat.2013.12.006]

12. Huang Ke-Jing, Yu Sheng, Li Jing, Wu Zhi-Wei, Wei Cai-Yun.  (2011)  Extraction of neurotransmitters from rat brain using graphene as a solid-phase sorbent, and their fluorescent detection by HPLC.  MICROCHIMICA ACTA,  176  (3): (327-335).  [PMID:] [10.1007/s00604-011-0719-8]