Procarbazine HCl - ≥98% , DNA inhibitor, CAS No.366-70-1, DNA inhibitor

Name: Procarbazine HCl - ≥98% , DNA inhibitor, CAS No.366-70-1, DNA inhibitor
Brand: Aladdin Scientific
SKU: P129854
Availability: InStock

CAS: 366-70-1 Cat. No.: P129854 Peso molecular: 257.76 Número EC: 206-678-6

COA

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Procarbazine HCl - ≥98% CAS No(366-70-1) by Aladdin Scientific

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Disponible para pedir

GRADE & PURITY ≥98%

Synonyms

Storage

Store at 2-8°C

Shipped In

Wet ice

Descripción general Specifications Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Calculadoras de soluciones Reseñas

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Why this grade

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

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Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Procarbazine HCl is a hydrochloride salt form of procarbazine which is a polyfunctional alkylating compound used as an antineoplastic agent.
An antineoplastic agent.

Specifications

Sinónimos

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

Primaquine phosphate is an antineoplastic agent.Clastogen and genotoxic carcinogen. Induces chromosomal damage and mutations. Antineoplastic agent. Active in vivo and in vitro.

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

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

INHIBITOR

Mecanismo de acción

DNA inhibitor

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 Sid	488181015
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488181015
Sonrisas canónicas	CC(C)NC(=O)C1=CC=C(C=C1)CNNC.Cl
IUPAC Name	4-[(2-methylhydrazinyl)methyl]-N-propan-2-ylbenzamide;hydrochloride
InChIKey	DERJYEZSLHIUKF-UHFFFAOYSA-N
INCHI	1S/C12H19N3O.ClH/c1-9(2)15-12(16)11-6-4-10(5-7-11)8-14-13-3;/h4-7,9,13-14H,8H2,1-3H3,(H,15,16);1H
Isómeros SMILES	CC(C)NC(=O)C1=CC=C(C=C1)CNNC.Cl
WGK Alemania	3
Peso molecular	257.76
Reaxy-Rn	4024454
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4024454&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

Kingdom Organic compounds
- Superclass Benzenoids
  - Clase Benzene and substituted derivatives
    - Subclass Benzoic acids and derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Clase	Benzene and substituted derivatives
Subclass	Benzoic acids and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Benzamides
Alternative Parents	Benzoyl derivatives Secondary carboxylic acid amides Alkylhydrazines Organopnictogen compounds Organooxygen compounds Organic oxides Hydrochlorides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Benzamide - Benzoyl - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Alkylhydrazine - Hydrochloride - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrazine derivative - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
Descripción	This compound belongs to the class of organic compounds known as benzamides. These are organic compounds containing a carboxamido substituent attached to a benzene ring.
External Descriptors	hydrochloride
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

Estructura 3D

Objetivos asociados (humanos)

A498 (42825 Activities)

Lot Number	Certificate Type	Fecha	Articulo
D23211567	Certificate of Analysis	Feb 07, 2025	P129854
D23211584	Certificate of Analysis	Feb 07, 2025	P129854
D23211585	Certificate of Analysis	Feb 07, 2025	P129854
D23211656	Certificate of Analysis	Feb 07, 2025	P129854
F1509100	Certificate of Analysis	Jan 25, 2023	P129854

Solubilidad	Soluble in water (52 mg/ml at 25 °C), DMSO (≥18 mg/ml), methanol, and ethanol (52 mg/ml at 25 °C).
Punto de fusión (°C)	226 °C
Peso molecular	257.760 g/mol
XLogP3
Hydrogen Bond Donor Count	4
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	5
Exact Mass	257.129 Da
Monoisotopic Mass	257.129 Da
Topological Polar Surface Area	53.200 Å²
Heavy Atom Count	17
Formal Charge	0
Complexity	210.000
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	2