Phenoxybenzamine HCl - ≥98% , Adrenergic receptor alpha antagonist, CAS No.63-92-3, Adrenergic receptor alpha antagonist

CAS: 63-92-3 Cat. No.: P129843 Peso molecular: 340.3 Número EC: 200-569-7
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
FT-0673569 | NCGC00093699-04 | NSC759572 | NSC-759572 | PHENOXYBENZAMINE HYDROCHLORIDE (IARC) | MLS002222313 | Tox21_302978 | CPD000058422 | N-2-Phenoxyisopropyl-N-benzyl-chloroethylamine hydrochloride | phenoxybenzamide hydrochloride | PHENOXYBENZAMINE H
Storage
Store at 2-8°C,Protected from light
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
P129843-1g
≥10

33,90US$

50,90US$
Guardar 17,00 US$ (33.40%)
5g
P129843-5g
4

137,90US$

206,90US$
Guardar 69,00 US$ (33.35%)
25g
P129843-25g
1

401,90US$

602,90US$
Guardar 201,00 US$ (33.34%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Protected from light Ships Wet ice 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Phenoxybenzamine HCl is a non-specific, irreversible alpha antagonist with an IC50 of 550 nM.
A non-specific irreversible adrenergic (AR) antagonist.

Specifications

Sinónimos
FT-0673569 | NCGC00093699-04 | NSC759572 | NSC-759572 | PHENOXYBENZAMINE HYDROCHLORIDE (IARC) | MLS002222313 | Tox21_302978 | CPD000058422 | N-2-Phenoxyisopropyl-N-benzyl-chloroethylamine hydrochloride | phenoxybenzamide hydrochloride | PHENOXYBENZAMINE H
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Phenoxybenzamine is a cell-permeable, non-specific, irreversible AR (α-adrenergic) antagonist that also acts as an CaM inhibitor. Phenoxybenzamine inhibits calmodulin-stimulated phosphodiesterase activity. This product has been shown to inhibit cGMP accum
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Tipo de acción
ANTAGONIST
Mecanismo de acción
Adrenergic receptor alpha antagonist
Nota
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.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488195285
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488195285
Sonrisas canónicasCC(COC1=CC=CC=C1)N(CCCl)CC2=CC=CC=C2.Cl
IUPAC NameN-benzyl-N-(2-chloroethyl)-1-phenoxypropan-2-amine;hydrochloride
InChIKeyVBCPVIWPDJVHAN-UHFFFAOYSA-N
INCHI1S/C18H22ClNO.ClH/c1-16(15-21-18-10-6-3-7-11-18)20(13-12-19)14-17-8-4-2-5-9-17;/h2-11,16H,12-15H2,1H3;1H
Isómeros SMILES CC(COC1=CC=CC=C1)N(CCCl)CC2=CC=CC=C2.Cl
WGK Alemania 3
RTECS DP3750000
Peso molecular 340.3
Reaxy-Rn 3747029
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3747029&ln=

Documentation

📋 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
SuperclassBenzenoids
ClaseBenzene and substituted derivatives
SubclassPhenylmethylamines
Intermediate Tree Nodes Not available
Direct ParentPhenylmethylamines
Alternative Parents Phenoxy compounds  Phenol ethers  Benzylamines  Aralkylamines  Alkyl aryl ethers  Trialkylamines  Organopnictogen compounds  Organochlorides  Hydrochlorides  Hydrocarbon derivatives  Alkyl chlorides  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzylamine - Phenol ether - Phenylmethylamine - Phenoxy compound - Alkyl aryl ether - Aralkylamine - Tertiary aliphatic amine - Tertiary amine - Ether - Organic nitrogen compound - Alkyl halide - Alkyl chloride - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Hydrochloride - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Amine - Aromatic homomonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenylmethylamines. These are compounds containing a phenylmethtylamine moiety, which consists of a phenyl group substituted by an methanamine.
External Descriptors organic molecular entity
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ABL1 Tclin Tyrosine-protein kinase ABL (18331 Activities)
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ESR1 Tclin Estrogen receptor alpha (17718 Activities)
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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
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ADRB2 Tclin Beta-2 adrenergic receptor (11824 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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VDR Tclin Vitamin D receptor (26531 Activities)
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GLA Tclin Alpha-galactosidase A (5444 Activities)
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S1PR1 Tclin Sphingosine 1-phosphate receptor Edg-1 (5806 Activities)
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POLK Tbio DNA polymerase kappa (8653 Activities)
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FFAR4 Tchem G-protein coupled receptor 120 (2999 Activities)
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APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
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BRD4 Tchem Bromodomain-containing protein 4 (13122 Activities)
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SMN1 Tchem Survival motor neuron protein (34246 Activities)
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LMNA Tbio Prelamin-A/C (36751 Activities)
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GPR35 Tchem G-protein coupled receptor 35 (2643 Activities)
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GMNN Tbio Geminin (128009 Activities)
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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
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MPHOSPH8 Tbio M-phase phosphoprotein 8 (656 Activities)
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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
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RAPGEF3 Tchem Rap guanine nucleotide exchange factor 3 (15528 Activities)
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Aplnr Apelin receptor (201 Activities)
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Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
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Mapk1 MAP kinase ERK2 (650 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

5 results found

Lot NumberCertificate TypeFechaArticulo
D2320876Certificate of AnalysisFeb 07, 2025 P129843
D2320877Certificate of AnalysisFeb 07, 2025 P129843
D2320879Certificate of AnalysisFeb 07, 2025 P129843
D2320938Certificate of AnalysisFeb 07, 2025 P129843
F1510058Certificate of AnalysisJan 25, 2023 P129843
Propiedades químicas y físicas
SolubilidadDMSO 68 mg/mL Water 17 mg/mL Ethanol 68 mg/mL
SensibilidadLight sensitive、Air sensitive
Punto de fusión (°C)139 °C
Peso molecular340.300 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count8
Exact Mass339.116 Da
Monoisotopic Mass339.116 Da
Topological Polar Surface Area12.500 Ų
Heavy Atom Count22
Formal Charge0
Complexity262.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
Calculadoras de soluciones
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