Hydralazine HCl - 2mM in Water , CAS No.304-20-1

CAS: 304-20-1 Cat. No.: H423147 Formula: C8H8N4·HCl Peso molecolare: 196.64 Numero EC: 206-151-0
Disponibile su ordine
GRADE & PURITY 2mM in Water
Synonyms
HYDRALAZINE HYDROCHLORIDE|304-20-1|HYDRALAZINE HCL|Apresoline|1-Hydrazinophthalazine hydrochloride|1-Hydrazinylphthalazine hydrochloride|Aiselazine|Dralzine|Hyperazin|Hyperex|Lopress|Hydralazine chloride|Slow-Apresolin|Apresine|Rolazine|Hydralazine monohy
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
Germania (EU)
USA*
Price
Qty
1ml
H423147-1ml
—
2 Disponibile

88,42€

130,07€
Salva 41,65 € (32.02%)
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Why this grade

2mM in Water for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

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

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Panoramica

Hydralazine HCl is a hydrochloride salt of hydralazine (Apresoline) that is a direct-acting smooth muscle relaxant with an IC50 of 1.9 mM.
An inhibitor of Dnmt, MAO-A/B, and amine oxidase.

Specifications

Sinonimi
HYDRALAZINE HYDROCHLORIDE | 304-20-1 | HYDRALAZINE HCL | Apresoline | 1-Hydrazinophthalazine hydrochloride | 1-Hydrazinylphthalazine hydrochloride | Aiselazine | Dralzine | Hyperazin | Hyperex | Lopress | Hydralazine chloride | Slow-Apresolin | Apresine | Rolazine | Hydralazine monohy
Specifiche e purezza
2mM in Water
Meccanismi biochimici e fisiologici
1-Hydrazinophthalazine Hydrochloride is a DNA methyltransferase (Dnmt) inhibitor which modulates epigenetic regulation of gene expression. 1-Hydrazinophthalazine Hydrochloride also acts as a non-selective MAO-A/B inhibitor and semicarbazide sensitive amin
Condizioni di conservazione di stoccaggio
Store at -80°C
Spedito in
Dry ice packs + Cold packs
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori
Pubchem Sid528754710
Sorrisi canoniciC1=CC=C2C(=C1)C=NN=C2NN.Cl
IUPAC Namephthalazin-1-ylhydrazine;hydrochloride
InChIKeyZUXNZUWOTSUBMN-UHFFFAOYSA-N
INCHI1S/C8H8N4.ClH/c9-11-8-7-4-2-1-3-6(7)5-10-12-8;/h1-5H,9H2,(H,11,12);1H
Isomeri SMILES C1=CC=C2C(=C1)C=NN=C2NN.Cl
WGK Germania 3
RTECS TH9000000
Peso molecolare 196.64
Reaxy-Rn 3568329
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3568329&ln=

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
SuperclassOrganoheterocyclic compounds
ClasseDiazanaphthalenes
SubclassBenzodiazines
Intermediate Tree Nodes Not available
Direct ParentPhthalazines
Alternative Parents Pyridazines and derivatives  Imidolactams  Benzenoids  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Hydrochlorides  Hydrocarbon derivatives  Hydrazines and derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Phthalazine - Imidolactam - Benzenoid - Pyridazine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Organonitrogen compound - Hydrazine derivative - Aromatic heteropolycyclic compound
DescrizioneThis compound belongs to the class of organic compounds known as phthalazines. These are compounds containing a phthalazine moiety, which consists of a benzene ring fused to a pyridazine, forming a 2,3-benzodiazine skeleton.
External Descriptors hydrochloride
Struttura 3D
Modello di struttura chimica interattiva





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Meccanismi d'azione
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)273°C(dec.)(lit.)
Peso molecolare196.640 g/mol
XLogP3
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count1
Exact Mass196.052 Da
Monoisotopic Mass196.052 Da
Topological Polar Surface Area63.800 Ų
Heavy Atom Count13
Formal Charge0
Complexity150.000
Isotope Atom Count0
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 Count2
Domande frequenti e articoli
Citations of This Product
Riferimenti
1. Xia Wang, Chenqian Zhou, Bingnan He, Baida Kong, Lai Wei, Rong Wang, Jiajia Lin, Yiyan Shao, Jianbo Zhu, Yuanxiang Jin, Zhengwei Fu.  (2019)  8:2 Fluorotelomer alcohol causes G1 cell cycle arrest and blocks granulocytic differentiation in HL-60 cells.  ENVIRONMENTAL TOXICOLOGY,  34  (5): (666-673).  [PMID:30794351] [10.1002/tox.22733]
2. Baida Kong, Xia Wang, Bingnan He, Lai Wei, Jianbo Zhu, Yuanxiang Jin, Zhengwei Fu.  (2018)  8:2 fluorotelomer alcohol inhibited proliferation and disturbed the expression of pro-inflammatory cytokines and antigen-presenting genes in murine macrophages.  CHEMOSPHERE,      [PMID:30558807] [10.1016/j.chemosphere.2018.12.091]
3. Zejian Kuang, Hongjun Luo, Hui Li, Yongyin Zhou, Zhexuan Lin, Wenhong Luo.  (2025)  Hydralazine Attenuates Lipopolysaccharide-Induced Murine Myocardial Dysfunction by Inhibition of Semicarbazide-Sensitive Amine Oxidase.  Antioxidants,  14  (12):   [PMID:41462702] [10.3390/antiox14121502]
Calcolatori di soluzioni
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