CHEMICAL AND PHYSICAL PROPERTIES
Physical Description | Solid |
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Melting Point | 223 °C |
Solubility | 1420 mg/L |
Vapor Pressure | 8.4X10-7 mm Hg @ 25 °C /Estimated/ |
LogP | 0.06 |
Henry's Law Constant | Henry's Law constant = 8.9X10-15 atm-cu m/mole @ 25 °C /Estimated/ |
Stability/Shelf Life | Procarbazine hydrochloride is unstable in aqueous solution. /Procarbazine hydrochloride/ |
Dissociation Constants | pKa = 6.6 |
Kovats Retention Index | 1990 1975 2000 1990 |
Other Experimental Properties | MW: 257.77. Crystals from methanol, mp 223-226 °C. /Hydrochloride/ |
SAFETY INFORMATION
Signal word | Warning |
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Pictogram(s) |
Exclamation Mark Irritant GHS07 Health Hazard GHS08 |
GHS Hazard Statements |
H302:Acute toxicity,oral H315:Skin corrosion/irritation H319:Serious eye damage/eye irritation H335:Specific target organ toxicity, single exposure;Respiratory tract irritation H351:Carcinogenicity H361:Reproductive toxicity |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. |
COMPUTED DESCRIPTORS
Molecular Weight | 221.30 g/mol |
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XLogP3 | 0.1 |
Hydrogen Bond Donor Count | 3 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 5 |
Exact Mass | 221.152812238 g/mol |
Monoisotopic Mass | 221.152812238 g/mol |
Topological Polar Surface Area | 53.2 Ų |
Heavy Atom Count | 16 |
Formal Charge | 0 |
Complexity | 210 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently-Bonded Unit Count | 1 |
Compound Is Canonicalized | Yes |
PRODUCT INTRODUCTION
description
Procarbazine is a benzamide obtained by formal condensation of the carboxy group of 4-[(2-methylhydrazino)methyl]benzoic acid with the amino group of isopropylamine. An antineoplastic chemotherapy drug used for treatment of Hodgkin's lymphoma. Metabolism yields azo-procarbazine and hydrogen peroxide, which results in the breaking of DNA strands. It has a role as an antineoplastic agent. It is a member of hydrazines and a member of benzamides. It is a conjugate base of a procarbazine(1+).