Exact Mass: 163.8809

Exact Mass Matches: 163.8809

Found 30 metabolites which its exact mass value is equals to given mass value 163.8809, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Molybdate

dihydroxydioxomolybdenumbis(ylium)

H2MoO4 (163.9007)


Molybdate is involved in the molybdenum cofactor biosynthesis pathway. Molybdate reacts with molybdopterin-AMP to produce molybdenum cofactor, AMP, and H2O. [HMDB]. Molybdate is found in many foods, some of which are okra, black raspberry, silver linden, and chinese chestnut. Molybdate is involved in the molybdenum cofactor biosynthesis pathway. Molybdate reacts with molybdopterin-AMP to produce molybdenum cofactor, AMP, and H2O.

   

Perchloroethylene

1,1,2,2-Tetrachloroethylene (acd/name 4.0)

C2Cl4 (163.8754)


Animal studies and a study of 99 twins by Dr. Samuel Goldman and researchers at the Parkinsons Institute in Sunnyvale, California determined there is a lot of circumstantial evidence that exposure to tetrachloroethene increases the risk of developing Parkinsons disease ninefold. Larger population studies are planned. Tetrachloroethene is a common soil contaminant. With a specific gravity greater than 1, tetrachloroethylene will be present as a dense nonaqueous phase liquid if sufficient quantities of liquid are spilled in the environment. Because of its mobility in groundwater, its toxicity at low levels, and its density (which causes it to sink below the water table), cleanup activities are more difficult than for oil spills. Recent research has focused on the in place remediation of soil and ground water pollution by tetrachloroethylene. Instead of excavation or extraction for above-ground treatment or disposal, tetrachloroethylene contamination has been successfully remediated by chemical treatment or bioremediation. Bioremediation has been successful under anaerobic conditions by reductive dechlorination by Dehalococcoides sp. and under aerobic conditions by cometabolism by Pseudomonas sp. Partial degradation daughter products include trichloroethylene, cis-1,2-dichloroethene and vinyl chloride; full degradation converts tetrachloroethylene to ethene and hydrogen chloride dissolved in water. Tetrachloroethylene is an excellent solvent for organic materials. Otherwise it is volatile, highly stable, and nonflammable. For these reasons, it is widely used in dry cleaning. Usually as a mixture with other chlorocarbons, it is also used to degrease metal parts in the automotive and other metalworking industries. It appears in a few consumer products including paint strippers and spot removers. Tetrachloroethylene, also known under the systematic name tetrachloroethene, or perchloroethylene (perc), and many other names, is a chlorocarbon with the formula Cl2C=CCl2. It is a colorless liquid widely used for dry cleaning of fabrics, hence it is sometimes called dry-cleaning fluid. It has a sweet odor detectable by most people at a concentration of 1 part per million (1 ppm). Worldwide production was about one million metric tons in 1985. The International Agency for Research on Cancer has classified tetrachloroethene as a Group 2A carcinogen, which means that it is probably carcinogenic to humans. Like many chlorinated hydrocarbons, tetrachloroethene is a central nervous system depressant and can enter the body through respiratory or dermal exposure. Tetrachloroethene dissolves fats from the skin, potentially resulting in skin irritation. This reaction can be catalyzed by a mixture of potassium chloride and aluminium chloride or by activated carbon. Trichloroethylene is a major byproduct, which is separated by distillation. D009676 - Noxae > D002273 - Carcinogens D004785 - Environmental Pollutants D012997 - Solvents

   

Chloral hydrate

1,1,1-Trichloro-2,2-dihydroxyethane

C2H3Cl3O2 (163.9199)


Chloral hydrate is a sedative and hypnotic drug as well as a chemical reagent and precursor. The name chloral hydrate indicates that it is formed from chloral (trichloroacetaldehyde) by the addition of one molecule of water. Its chemical formula is C2H3Cl3O2. It was discovered through the chlorination of ethanol in 1832 by Justus von Liebig in Gießen. Its sedative properties were first published in 1869 and subsequently, because of its easy synthesis, its use was widespread. (Wikipedia) D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D006993 - Hypnotics and Sedatives N - Nervous system > N05 - Psycholeptics > N05C - Hypnotics and sedatives > N05CC - Aldehydes and derivatives C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2199 - Adjuvant Analgesic

   

Sodium phosphate (Na3PO4)

Phosphoric acid, trisodium salt , dodecahydrate

Na3O4P (163.9227)


Nutrient supplement, pH control agent, sequestrant, stabiliser, protein modifier, emulsifier in production of processed cheeses, indirect food additive arising from use as a boiler water additive B - Blood and blood forming organs > B05 - Blood substitutes and perfusion solutions > B05X - I.v. solution additives > B05XA - Electrolyte solutions A - Alimentary tract and metabolism > A06 - Drugs for constipation > A06A - Drugs for constipation > A06AD - Osmotically acting laxatives V - Various > V03 - All other therapeutic products > V03A - All other therapeutic products > V03AG - Drugs for treatment of hypercalcemia A - Alimentary tract and metabolism > A06 - Drugs for constipation > A06A - Drugs for constipation > A06AG - Enemas C78275 - Agent Affecting Blood or Body Fluid > C29730 - Electrolyte Replacement Agent

   

Dysprosium

Dysprosium

Dy (163.9292)


Dysprosium, also known as 66dy or disprosio, is a member of the class of compounds known as homogeneous lanthanide compounds. Homogeneous lanthanide compounds are inorganic compounds containing only metal atoms, with the largest atom being a lanthanide atom. Dysprosium can be found in red beetroot, romaine lettuce, and spinach, which makes dysprosium a potential biomarker for the consumption of these food products. Dysprosium was first identified in 1886 by Paul √âmile Lecoq de Boisbaudran, but it was not isolated in pure form until the development of ion exchange techniques in the 1950s. Dysprosium has relatively few applications where it cannot be replaced by other chemical elements. It is used for its high thermal neutron absorption cross-section in making control rods in nuclear reactors, for its high magnetic susceptibility in data storage applications, and as a component of Terfenol-D (a magnetostrictive material). Soluble dysprosium salts are mildly toxic, while the insoluble salts are considered non-toxic . Dysprosium, also known as 66dy or disprosio, is a member of the class of compounds known as homogeneous lanthanide compounds. Homogeneous lanthanide compounds are inorganic compounds containing only metal atoms, with the largest atom being a lanthanide atom. Dysprosium can be found in red beetroot, romaine lettuce, and spinach, which makes dysprosium a potential biomarker for the consumption of these food products. Dysprosium was first identified in 1886 by Paul Émile Lecoq de Boisbaudran, but it was not isolated in pure form until the development of ion exchange techniques in the 1950s. Dysprosium has relatively few applications where it cannot be replaced by other chemical elements. It is used for its high thermal neutron absorption cross-section in making control rods in nuclear reactors, for its high magnetic susceptibility in data storage applications, and as a component of Terfenol-D (a magnetostrictive material). Soluble dysprosium salts are mildly toxic, while the insoluble salts are considered non-toxic .

   

Molybdate

molybdate ion

H2MoO4 (163.9007)


   

bromochlorodifluoromethane

bromochlorodifluoromethane

CBrClF2 (163.884)


D005411 - Flame Retardants

   

2-Bromo-1,3,4-thiadiazole

2-Bromo-1,3,4-thiadiazole

C2HBrN2S (163.9044)


   

sodium aluminum oxide

Sodium aluminium oxide (NaAlO2)

Al2Na2O4 (163.9223)


Food contaminant arising from its use as a boiler water additive in the prepn. of steam for food processing

   

Nickel(2+) ethanedioate hydrate (1:1:1)

Nickel(2+) ethanedioate hydrate (1:1:1)

C2H2NiO5 (163.9256)


   

5-Bromo-1,2,4-thiadiazole

5-Bromo-1,2,4-thiadiazole

C2HBrN2S (163.9044)


   

cesium methoxide

cesium methoxide

CH3CsO (163.9238)


   

Tetrachloroethylene-13C1

Tetrachloroethylene-13C1

C2Cl4 (163.8754)


   

cobalt trichloride

cobalt trichloride

Cl3Co (163.8398)


   

sodium dihydrogen arsenate

sodium dihydrogen arsenate

AsH2NaO4 (163.9067)


D010575 - Pesticides > D007306 - Insecticides D016573 - Agrochemicals

   

Chloromethyl chlorosulfate

Chloromethyl chlorosulfate

CH2Cl2O3S (163.9102)


   

Copper(1+) trifluoromethanethiolate

Copper(1+) trifluoromethanethiolate

CCuF3S (163.8969)


   

sodium,oxido(dioxo)niobium

sodium,oxido(dioxo)niobium

NaNbO3 (163.8809)


   

nickel oxide, black

nickel oxide, black

Ni2O3 (163.8554)


   

O-methyl dichlorothiophosphate

O-methyl dichlorothiophosphate

CH3Cl2OPS (163.9019)


   

TRICHLOROACETYL FLUORIDE

TRICHLOROACETYL FLUORIDE

C2Cl3FO (163.8999)


   

Monosodium phosphate

Monosodium phosphate

Na3O4P (163.9227)


   

strontium metasilicate

strontium metasilicate

O3SiSr (163.8673)


   

Tetracarbonylchromium(0)

Tetracarbonylchromium(0)

C4CrO4 (163.9202)


   

trisodium phosphate

trisodium phosphate

Na3O4P (163.9227)


B - Blood and blood forming organs > B05 - Blood substitutes and perfusion solutions > B05X - I.v. solution additives > B05XA - Electrolyte solutions A - Alimentary tract and metabolism > A06 - Drugs for constipation > A06A - Drugs for constipation > A06AD - Osmotically acting laxatives V - Various > V03 - All other therapeutic products > V03A - All other therapeutic products > V03AG - Drugs for treatment of hypercalcemia A - Alimentary tract and metabolism > A06 - Drugs for constipation > A06A - Drugs for constipation > A06AG - Enemas C78275 - Agent Affecting Blood or Body Fluid > C29730 - Electrolyte Replacement Agent

   

Dysprosium

Dysprosium

Dy (163.9292)


   

Tellurinic acid

Tellurinic acid

H2O2Te (163.9117)


   

chloral hydrate

chloral hydrate

C2H3Cl3O2 (163.9199)


D002491 - Central Nervous System Agents > D002492 - Central Nervous System Depressants > D006993 - Hypnotics and Sedatives N - Nervous system > N05 - Psycholeptics > N05C - Hypnotics and sedatives > N05CC - Aldehydes and derivatives C78272 - Agent Affecting Nervous System > C241 - Analgesic Agent > C2199 - Adjuvant Analgesic An organochlorine compound that is the hydrate of trichloroacetaldehyde.

   

TETRACHLOROETHYLENE

TETRACHLOROETHYLENE

C2Cl4 (163.8754)


D009676 - Noxae > D002273 - Carcinogens D004785 - Environmental Pollutants D012997 - Solvents

   

Molybdic acid

Molybdic(VI) acid

H2MoO4 (163.9007)