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Forensic chemistry is the application of chemistry and its subfield, forensic toxicology, in a legal setting. A forensic chemist can assist in the identification of unknown materials found at a crime scene. [1] Specialists in this field have a wide array of methods and instruments to help identify unknown substances.
Pages in category "Forensic chemicals" The following 7 pages are in this category, out of 7 total. This list may not reflect recent changes. A. 3-Aminophthalic acid; B.
Post-mortem chemistry, also called necrochemistry or death chemistry, is a subdiscipline of chemistry in which the chemical structures, reactions, processes and parameters of a dead organism is investigated. Post-mortem chemistry plays a significant role in forensic pathology.
Luminol (C 8 H 7 N 3 O 2) is a chemical that exhibits chemiluminescence, with a blue glow, when mixed with an appropriate oxidizing agent.Luminol is a white-to-pale-yellow crystalline solid that is soluble in most polar organic solvents but insoluble in water.
A bone saw is used for cutting bones. Sternal saw: for cutting into the chest of the body by cutting the sternum. Toothed forceps: for tearing or holding structures Mallet: used as a hammer: Autopsy hammer: used just as a hammer Skull key: a T-shaped chisel used as a lever while removing skull cap [2] Brain knife: to cleanly cut the brain Rib ...
Forensic toxicology is a multidisciplinary field that combines the principles of toxicology with expertise in disciplines such as analytical chemistry, pharmacology and clinical chemistry to aid medical or legal investigation of death, poisoning, and drug use. [1] The paramount focus for forensic toxicology is not the legal implications of the ...
Alex J. Krotulski, who runs the toxicology and chemistry lab at the Center for Forensic Science Research & Education in Horsham, Pennsylvania, analyzes samples for police and other clients.
Ninhydrin (2,2-dihydroxyindane-1,3-dione) is an organic compound with the formula C 6 H 4 (CO) 2 C(OH) 2.It is used to detect ammonia and amines.Upon reaction with these amines, ninhydrin gets converted into deep blue or purple derivatives, which are called Ruhemann's purple.