Exact Mass: 71.0609

Exact Mass Matches: 71.0609

Found 50 metabolites which its exact mass value is equals to given mass value 71.0609, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Acrylamide

American cyanamid P-250

C3H5NO (71.0371)


Acrylamide (or acrylic amide) is an organic compound with the chemical formula CH2=CHC(O)NH2. It is a white odorless solid, soluble in water and several organic solvents. It is produced industrially as a precursor to polyacrylamides, which find many uses as water-soluble thickeners and flocculation agents. It is highly toxic, likely to be carcinogenic,and partly for that reason it is mainly handled as an aqueous solution. It is a chemical used in many industries around the world and more recently was found to form naturally in foods cooked at high temperatures. Acrylamide is a neurotoxicant, reproductive toxicant, and carcinogen in animal species. Only the neurotoxic effects have been observed in humans and only at high levels of exposure in occupational settings. The mechanism underlying neurotoxic effects of ACR may be basic to the other toxic effects seen in animals. This mechanism involves interference with the kinesin-related motor proteins in nerve cells or with fusion proteins in the formation of vesicles at the nerve terminus and eventual cell death. Neurotoxicity and resulting behavioral changes can affect reproductive performance of ACR-exposed laboratory animals with resulting decreased reproductive performance. Further, the kinesin motor proteins are important in sperm motility, which could alter reproduction parameters. Effects on kinesin proteins could also explain some of the genotoxic effects on ACR. These proteins form the spindle fibers in the nucleus that function in the separation of chromosomes during cell division. This could explain the clastogenic effects of the chemical noted in a number of tests for genotoxicity and assays for germ cell damage. Other mechanisms underlying ACR-induced carcinogenesis or nerve toxicity are likely related to an affinity for sulfhydryl groups on proteins. Binding of the sulfhydryl groups could inactive proteins/enzymes involved in DNA repair and other critical cell functions. Direct interaction with DNA may or may not be a major mechanism for cancer induction in animals. The DNA adducts that form do not correlate with tumor sites and ACR is mostly negative in gene mutation assays except at high doses that may not be achievable in the diet. All epidemiologic studies fail to show any increased risk of cancer from either high-level occupational exposure or the low levels found in the diet. In fact, two of the epidemiologic studies show a decrease in cancer of the large bowel. A number of risk assessment studies were performed to estimate increased cancer risk. The results of these studies are highly variable depending on the model. There is universal consensus among international food safety groups in all countries that examined the issue of ACR in the diet that not enough information is available at this time to make informed decisions on which to base any regulatory action. Too little is known about levels of this chemical in different foods and the potential risk from dietary exposure. Avoidance of foods containing ACR would result in worse health issues from an unbalanced diet or pathogens from under cooked foods. There is some consensus that low levels of ACR in the diet are not a concern for neurotoxicity or reproductive toxicity in humans, although further research is need to study the long-term, low-level cumulative effects on the nervous system. Any relationship to cancer risk from dietary exposure is hypothetical at this point and awaits more definitive studies. (PMID:17492525). Polyacrylamides are used as flocculants as a filtration aid in the treatment of waste water and expressed sugar juices and as clarifying agents in a variety of food products. Asparagine-derived Maillard production found in trace amounts in a variety of cooked and processed foods. Subject of a food scare in 2001-2 but concern may have been overstated.

   

3-Buten-1-amine

3-Buten-1-amine

C4H9N (71.0735)


   

Pyrrolidine

Pyrrolidine hydrochloride

C4H9N (71.0735)


Pyrrolidine is found in alcoholic beverages. Pyrrolidine is widely distributed in foodstuffs in trace amts., presumably as bacterial decarboxylation produced of proline. Pyrrolidine is present in bread, milk, cheese, carrots, celery stalks, beer, spirits, coffee, caviar and fatty fish. Pyrrolidine is a flavouring agent.Pyrrolidine is a clear liquid with an unpleasant odor that is ammoniacal, fishy, shellfish-like and seaweed-like. Pyrrolidine is found naturally in the leaves of tobacco and carrot. The pyrrolidine ring structure is present in numerous natural alkaloids such as nicotine and hygrine. It is found in many pharmaceutical drugs such as procyclidine and bepridil. It also forms the basis for the racetam compounds (e.g. piracetam, aniracetam). Pyrrolidine is a pyrrolidine ring is the central structure of the amino acids proline and hydroxyproline. (Wikipedia) Pyrrolidine has been found to be a metabolite in Xenorhabdus (PMID: 19598185). Prolamins are a group of plant storage proteins having a high proline content and found in the seeds of cereal grains: wheat (gliadin), barley (hordein), rye (secalin), corn (zein) and as a minor protein, avenin in oats. They are characterised by a high glutamine and proline content and are generally soluble only in strong alcohol solutions. Some prolamins, notably gliadin, and similar proteins found in the tribe Triticeae (see Triticeae glutens) may induce coeliac disease in genetically predisposed individuals.

   

1-Ethylaziridine

Ethylethyleneimine

C4H9N (71.0735)


   

3-Hydroxypropionitrile

3-hydroxypropanenitrile

C3H5NO (71.0371)


   

2-Azetidinone

4-Carboxy-2-azetidinone

C3H5NO (71.0371)


   

1-Carboxyethyl

prop-2-enoyloxidanyl

C3H3O2 (71.0133)


   

Dihydrotriazole

2,3-dihydro-1H-1,2,3-triazole

C2H5N3 (71.0483)


   

Ethyl isocyanate

Isocyanic acid, ethyl ester

C3H5NO (71.0371)


   

hydroxybutyl

hydroxybutyl

C4H7O (71.0497)


   

isoamyl

3-methylbutyl

C5H11 (71.0861)


   

Isoxazoline

4,5-dihydro-1,2-oxazole

C3H5NO (71.0371)


   

Oxazoline

4,5-dihydro-1,3-oxazole

C3H5NO (71.0371)


   

n-Pentyl

n-Pentyl

C5H11 (71.0861)


   

Nitrile-(()-2-Hydroxypropanoic acid

Nitrile-(()-2-Hydroxypropanoic acid

C3H5NO (71.0371)


   

2-propenal oxime

2-propenal oxime

C3H5NO (71.0371)


   

Acrylamide Crystals

Acrylamide Crystals

C3H5NO (71.0371)


   

PYRROLIDINE

PYRROLIDINE

C4H9N (71.0735)


MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; RWRDLPDLKQPQOW-UHFFFAOYSA-N_STSL_0187_Pyrrolidine_2000fmol_180831_S2_L02M02_76; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I.

   

Azolidine

Tetramethylenimine

C4H9N (71.0735)


   

oxazolin

4,5-dihydrooxazole

C3H5NO (71.0371)


   

3-Azetidinone

3-Azetidinone

C3H5NO (71.0371)


   

N-Methylcyclopropylamine

N-Methylcyclopropylamine

C4H9N (71.0735)


   

Methoxyacetonitrile

Methoxyacetonitrile

C3H5NO (71.0371)


   

ethyl cyanate

ethyl cyanate

C3H5NO (71.0371)


   

Crotylamine

Crotylamine

C4H9N (71.0735)


   

(1-13C)-2-Propenamide

(1-13C)-2-Propenamide

C3H5NO (71.0371)


   

O-prop-2-ynylhydroxylamine

O-prop-2-ynylhydroxylamine

C3H5NO (71.0371)


   

N-Vinylformamide

N-Vinylformamide

C3H5NO (71.0371)


   

azetidinone

2-Azetidinone

C3H5NO (71.0371)


   

Lactonitrile

2-hydroxypropionitrile

C3H5NO (71.0371)


   

pyrrole-2,3,4,5-d4

pyrrole-2,3,4,5-d4

C4HD4N (71.0673)


   

1-Cyclopropylmethanamine

1-Cyclopropylmethanamine

C4H9N (71.0735)


   

2-Methylallylamine

2-Methylallylamine

C4H9N (71.0735)


   

N-Allylmethylamine

N-Allylmethylamine

C4H9N (71.0735)


   

Azetidine, 3-methyl-

Azetidine, 3-methyl-

C4H9N (71.0735)


   

1-Methylcyclopropanamine

1-Methylcyclopropanamine

C4H9N (71.0735)


   

(+/-)-2-CHLORO-N-(2,6-DIMETHYLPHENYL)-N-(TETRAHYDRO-2-OXO-3-FURANYL)-ACETAMIDE

(+/-)-2-CHLORO-N-(2,6-DIMETHYLPHENYL)-N-(TETRAHYDRO-2-OXO-3-FURANYL)-ACETAMIDE

C4H9N (71.0735)


   

Ethyl isocyanate

Ethyl isocyanate

C3H5NO (71.0371)


   

Cyclobutanamine

Cyclobutanamine

C4H9N (71.0735)


   

Aziridine,2,2-dimethyl-

Aziridine,2,2-dimethyl-

C4H9N (71.0735)


   

Aziridine, 2-ethyl-

Aziridine, 2-ethyl-

C4H9N (71.0735)


   

Acrylate

Acrylate

C3H3O2- (71.0133)


D001697 - Biomedical and Dental Materials > D014014 - Tissue Adhesives

   

n-Pentyl

n-Pentyl

C5H11 (71.0861)


   

Dihydrotriazole

Dihydrotriazole

C2H5N3 (71.0483)


   

1,2,3-Triazoline

1,2,3-Triazoline

C2H5N3 (71.0483)


   

2,3-dihydro-1H-1,2,4-triazole

2,3-dihydro-1H-1,2,4-triazole

C2H5N3 (71.0483)


   

Polyacrylamide

Polyacrylamide

C3H5NO (71.0371)


Polyacrylamide (IUPAC poly(2-propenamide) or poly(1-carbamoylethylene)) is a polymer (-CH2CHCONH2-) formed from acrylamide subunits. It can be synthesized as a simple linear-chain structure or cross-linked, typically using N,N-methylenebisacrylamide.

   

beta-Ammoniopropionitrile

beta-Ammoniopropionitrile

C3H7N2+ (71.0609)


A primary ammonium ion obtained by protonation of the amino function of beta-aminopropionitrile.

   

2-Ammoniopropanenitrile

2-Ammoniopropanenitrile

C3H7N2+ (71.0609)


   

Butenamine

Butenamine

C4H9N (71.0735)