Exact Mass: 124.991939734

Exact Mass Matches: 124.991939734

Found 17 metabolites which its exact mass value is equals to given mass value 124.991939734, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Trimethylselenonium

Trimethylselenonium nitrate, (75)se-labeled

C3H9Se+ (124.9869424)


Trimethylselenonium belongs to the family of Aliphatic Acyclic Compounds. These are organic compounds that is aliphatic (non-aromatic) and does not contain a ring.

   

Bentonite

alumane hydrate magnesium silane sodium hydrogen

AlH7MgNaOSi (124.98297620000001)


It is used in foods as a colourant, pigment and stabiliser↵↵Also known as potash bentonite or K-bentonite, potassium bentonite is a potassium rich illitic clay formed from alteration of volcanic ash.; Bentonite is an absorbent aluminium phyllosilicate, generally impure clay consisting mostly of montmorillonite. There are a few types of bentonites and their names depend on the dominant elements, such as K, Na, Ca, and Al. As noted in several places in the geologic literature, there are some nomenclatorial problems with the classification of bentonite clays. Bentonite usually forms from weathering of volcanic ash, most often in the presence of water. However, the term bentonite, as well as a similar clay called tonstein, have been used for clay beds of uncertain origin. For industrial purposes, two main classes of bentonite exist: sodium and calcium bentonite. In stratigraphy and tephrochronology, completely devitrified (weathered volcanic glass) ash-fall beds are commonly referred to as K-bentonites when the dominant clay species is illite. Other common clay species, and sometimes dominant, are montmorillinite and kaolinite. Kaolinite dominated clays are commonly referred to as tonsteins and are typically associated with coal.; Bentoquatam protects the skin like a shield against poison ivy, poison oak, and poison sumac by physically blocking skin contact with their resin. The best protection against getting these conditions is to avoid contact with these plants. This medicine does not dry oozing and weeping caused by the rash of poison ivy, poison oak, or poison sumac.; Calcium bentonite is a useful adsorbent of ions in solution. as well as fats and oils, being a main active ingredient of Fullers Earth, probably one of the earliest industrial cleaning agents. Calcium bentonite may be converted to sodium bentonite (termed sodium beneficiation or sodium activation) to exhibit many of sodium bentonites properties by a process known as "ion exchange" (patented in 1935 by Germans U Hofmann and K Endell). Commonly this means adding 5-10\\% of a soluble sodium salt such as sodium carbonate to wet bentonite, mixing well, and allowing time for the ion exchange to take place and water to remove the exchanged calcium.[citation needed] Some properties, such as viscosity and fluid loss of suspensions, of sodium beneficiated calcium bentonite (or sodium activated bentonite) may not be fully equivalent to natural sodium bentonite. For example, residual calcium carbonates (formed if exchanged cations are insufficiently removed) may result in inferior performance of the bentonite in geosynthetic liners; Much of bentonites usefulness in the drilling and geotechnical engineering industry comes from its unique rheological properties. Relatively small quantities of bentonite suspended in water form a viscous, shear thinning material. Most often, bentonite suspensions are also thixotropic, although rare cases of rheopectic behavior have also been reported. At high enough concentrations (~60 grams of bentonite per litre of suspension), bentonite suspensions begin to take on the characteristics of a gel (a fluid with a minimum yield strength required to make it move). For these reasons it is a common component of drilling mud used to curtail drilling fluid invasion by its propensity for aiding in the formation of mud cake.; Pascalite is a commercial name for the calcium bentonite clay. Bentonite is found in wild celery.

   

trimethylselanium

Trimethylselenonium

C3H9Se+ (124.9869424)


   

3-bromo-1,1,1-trideuteriopropane

3-bromo-1,1,1-trideuteriopropane

C3H4BrD3 (124.991939734)


   
   

3-Thienyl Isocyanate

3-Thienyl Isocyanate

C5H3NOS (124.9935348)


   

Methanamine, N-methyl-,hydrobromide (9CI)

Methanamine, N-methyl-,hydrobromide (9CI)

C2H8BrN (124.9840068)


   

Ethylamine (HBr)

Ethylamine (HBr)

C2H8BrN (124.9840068)


   

2-Thienyl Isocyanate

2-Thienyl Isocyanate

C5H3NOS (124.9935348)


   

Ethyl sulphate

Ethyl sulphate

C2H5O4S- (124.990855)


D009676 - Noxae > D000477 - Alkylating Agents D009676 - Noxae > D009153 - Mutagens

   

Isethionate

Isethionate

C2H5O4S- (124.990855)


The alkanesulfonate that is the anion formed from isethionic acid by loss of a proton from the sulfo group; major microspecies at pH 7.3.

   

2-Hydroxyethylphosphonic acid(1-)

2-Hydroxyethylphosphonic acid(1-)

C2H6O4P- (125.00037060000001)


   

(R)-(1-hydroxyethyl)phosphonate

(R)-(1-hydroxyethyl)phosphonate

C2H6O4P- (125.00037060000001)


   
   

2-Hydroxyethyl sulfonate

2-Hydroxyethyl sulfonate

C2H5O4S- (124.990855)


   

Trimethylselenonium

Trimethylselenonium

C3H9Se+ (124.9869424)


An organic cation consisting of three methyl groups covalently bound to a central selenium atom.

   

ethyl hydrogen phosphate(1-)

ethyl hydrogen phosphate(1-)

C2H6O4P (125.00037060000001)


An organophosphate oxoanion that is the conjugate base of ethyl dihydrogen phosphate arising from deprotonation of one of the OH groups of the phosphate.