Exact Mass: 90.054

Exact Mass Matches: 90.054

Found 33 metabolites which its exact mass value is equals to given mass value 90.054, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Diethyl sulfide

1-(Ethylsulphanyl)ethane

C4H10S (90.0503)


Diethyl sulfide is found in alcoholic beverages. Diethyl sulfide is a food additive listed in the EAFUS food Additive Database (Jan 2001). Diethyl sulfide is found in various foods and brandies. Diethyl sulfide is a food flavour ingredient. Diethyl sulfide is a clear, flammable chemical compound with a pungent garlic-like odor. It has the chemical formula C4H10S. It is prepared by treating ethanol with concentrated sulfuric acid, partially neutralizing the new solution with sodium carbonate, then distilling the resulting sodium ethyl sulfate in a solution containing potassium sulfide Food additive listed in the EAFUS Food Additive Database (Jan 2001). Found in various foods and brandies. Food flavour ingredient

   

2-(Methylthio)propane

Isopropyl methyl sulfide, 8ci

C4H10S (90.0503)


2-(Methylthio)propane is produced by some canned vegetables. Produced by some canned vegetables

   

1-Butanethiol

N-Butyl mercaptan, 1,2-(14)C,2-(35) S-labeled CPD

C4H10S (90.0503)


1-Butanethiol, also known as 1-butyl mercaptan or 1-butylthiol, belongs to the class of organic compounds known as alkylthiols. These are organic compounds containing the thiol functional group linked to an alkyl chain. 1-Butanethiol is a coffee, egg, and garlic tasting compound. 1-Butanethiol has been detected, but not quantified, in milk and milk products and potato. Commercially, this is performed using ultraviolet light. It is sometimes placed in the "stink bombs" and "stink perfumes" for pranksters. Butanethiol is a very noxious and caustic chemical compound, and at sufficiently high concentrations, it produces serious health effects in both humans and animals, especially as a result of prolonged exposure. It may cause effects on the thyroid and the nervous system and could cause lowering of consciousness. The scent of butanethiol is so strong that the human nose can easily detect it in the air at concentrations as low as 10 parts per billion. The substance irritates the eyes, the skin, and the respiratory tract. Butanethiol is a thiol of low molecular weight, and it is highly flammable. Butanethiol is used as an industrial solvent, and as an intermediate for cotton defoliants. The threshold level for 1-butanethiol is reported as 1.4 ppb. Butanethiol is chemically classified among the thiols, which are organic compounds with molecular formulas and structural formulas similar to alcohols, except that sulfur-containing sulfhydryl group (-SH) replaces the oxygen-containing hydroxyl group (-OH) in the molecule. Butanethiol is prepared by the free radical catalyzed addition of hydrogen sulfide to 1-butene. Contact with the skin and mucous membranes causes burns, and contact with the eyes can lead to blurred vision or complete blindness. Inhalation may cause weakness, confusion, cough, dizziness, drowsiness, headache, nausea, vomiting, and shortness of breath. 1-Butanethiol is a flavouring agent. It is found in animal foods such as beef and raw chicken. It is also found in cooked potatoes and in milk and milk products (e.g. Cheshire cheese).

   

2-Methyl-1-propanethiol

1-mercapto-2-Methylpropane

C4H10S (90.0503)


2-Methyl-1-propanethiol is found in alcoholic beverages. 2-Methyl-1-propanethiol is a food additive listed in the EAFUS food Additive Database (Jan. 2001). 2-Methyl-1-propanethiol is found in guava, milk, cooked beef, cooked pork and beer. 2-Methyl-1-propanethiol is a flavouring ingredien Food additive listed in the EAFUS Food Additive Database (Jan. 2001). Found in guava, milk, cooked beef, cooked pork and beer. Flavouring ingredient

   

1-(Methylthio)-propane

1-(methylsulfanyl)propane

C4H10S (90.0503)


1-(Methylthio)-propane belongs to the class of organic compounds known as dialkylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two alkyl groups.

   

2-Butanethiol

butane-2-thiol

C4H10S (90.0503)


   

Butylphosphine

butylphosphane

C4H11P (90.0598)


   

Carbohydrazide

Hydrazide hydrazinecarboxylic acid

CH6N4O (90.0542)


   

2-Butanethiol

2-Butanethiol

C4H10S (90.0503)


   

iso-C4H9SH

1-mercapto-2-Methylpropane

C4H10S (90.0503)


   

Butylthiol

N-Butyl mercaptan, 1,2-(14)C,2-(35) S-labeled CPD

C4H10S (90.0503)


   

Isobutanethiol

Isopropyl methyl sulfide, 8ci

C4H10S (90.0503)


   

3-fluorobutan-2-one

3-fluorobutan-2-one

C4H7FO (90.0481)


   

L-Alanine (2-D)

L-Alanine (2-D)

C3H6DNO2 (90.054)


   

3-Fluorocyclobutanol

3-Fluorocyclobutanol

C4H7FO (90.0481)


   

Methyl propyl sulfide

N-PROPYLMETHYLSULFIDE

C4H10S (90.0503)


1-(methylthio)-propane is a member of the class of compounds known as dialkylthioethers. Dialkylthioethers are organosulfur compounds containing a thioether group that is substituted by two alkyl groups. 1-(methylthio)-propane is an alliaceous, creamy, and green tasting compound found in kohlrabi, which makes 1-(methylthio)-propane a potential biomarker for the consumption of this food product. 1-(methylthio)-propane can be found primarily in feces and saliva.

   

4-fluorobutyraldehyde

4-fluorobutyraldehyde

C4H7FO (90.0481)


   

D-(2-2H)Alanine

D-(2-2H)Alanine

C3H6DNO2 (90.054)


   

Trimethylsilanol

Trimethylsilanol

C3H10OSi (90.0501)


   

DL-Alanine (2-D)

DL-Alanine (2-D)

C3H6DNO2 (90.054)


   

Tert-Butylthiol

tert-Butyl mercaptan

C4H10S (90.0503)


   

Cis-2-fluorocyclopropyl)methanol

Cis-2-fluorocyclopropyl)methanol

C4H7FO (90.0481)


   

(trans-2-fluorocyclopropyl)methanol

(trans-2-fluorocyclopropyl)methanol

C4H7FO (90.0481)


   

tert-butylphosphane

tert-butylphosphane

C4H11P (90.0598)


   

Diethylphosphine

Diethylphosphine

C4H11P (90.0598)


   

Bicyclo[4.1.0]hepta-1,3,5-triene

Bicyclo[4.1.0]hepta-1,3,5-triene

C7H6 (90.0469)


   

L-alaninium

L-alaninium

C3H8NO2+ (90.0555)


The L-enantiomer of alaninium.

   

Sarcosinium

Sarcosinium

C3H8NO2+ (90.0555)


An alpha-amino-acid cation that is the conjugate acid of sarcosine, arising from protonation of the amino group.

   

Alaninium

Alaninium

C3H8NO2+ (90.0555)


An alpha-amino-acid cation that is the conjugate acid of alanine.

   

D-alaninium

D-alaninium

C3H8NO2+ (90.0555)


An alaninium that is the conjugate acid of D-alanine.

   

Diethyl sulfide

Diethyl sulfide

C4H10S (90.0503)


   

butanethiol

1-Butanethiol

C4H10S (90.0503)


   

carbohydrazide

carbohydrazide

CH6N4O (90.0542)