Sarcosine supplier | CasNO.107-97-1

Name
Sarcosine
EINECS 203-538-6
CAS No. 107-97-1
Article Data122
CAS DataBase
Density 1.093 g/cm³
Solubility 1480 g/L (20 °C) in water
Melting Point 208-212 °C (dec.)(lit.)
Formula C₃H₇NO₂
Boiling Point 195.1 °C at 760 mmHg
Molecular Weight 89.0941
Flash Point 71.8 °C
Transport Information
Appearance white crystalline powder
Safety 24/25-36-26
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Sarcosine(8CI);(Methylamino)acetic acid;(Methylamino)ethanoic acid;2-(Methylamino)acetic acid;Acetic acid, (methylamino)-;Methylglycine;N-Methylaminoaceticacid;N-Methylglycine;Sarcosin;Sarcosinic acid;
PSA 49.33000
LogP -0.31870

Synthetic route

: 14031-35-7, 17176-17-9, 29908-03-0, 75044-81-4, 78548-84-2, 79647-17-9, 91279-78-6
S-Adenosyl-L-methionine

: 56-40-6
glycine

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With recombinant mouse glycine N-methyltransferase In aq. buffer at 30℃; for 0.333333h; pH=8; Reagent/catalyst; Enzymatic reaction;

: 5616-81-9
sarcosine tert-butyl ester

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With trifluoroacetic acid In dichloromethane at 20℃; for 2h;

: 107-16-4
glycolonitrile

: 74-89-5
methylamine

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With water das entstechende Nitril wird durch konz. Salzsaeure verseift;
With water; sodium hydroxide at 25℃; for 1h; Inert atmosphere;
Stage #1: glycolonitrile; methylamine at 20℃; for 1h; Inert atmosphere; Stage #2: With water; sodium hydroxide

: 52605-49-9
sarcosine ethyl ester hydrochloride

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With bromine; triethylamine In dichloromethane; water; ethyl acetate

: 50-00-0
formaldehyd

: 56-40-6
glycine

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With sodium dihydrogenphosphate; zinc at 30℃; for 0.116667h;	90%
With hydrogenchloride; water

: 1083159-08-3
O2-(2,4-dinitrophenyl) 1-[N-(carboxymethyl)-N-methylamino]diazen-1-ium-1,2-diolate

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With GLUTATHIONE; diethylenetriaminopentaacetic acid In dimethyl sulfoxide at 37℃; pH=7.4; aq. phosphate buffer; Inert atmosphere;

: 1071-83-6
N-(phosphonemethyl)glycine

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With Pseudomonas putida T5 glyphosate C-P lyase In aq. phosphate buffer at 30℃; pH=7; Kinetics; Enzymatic reaction;

: 76110-01-5
luzopeptin C

A: 107-97-1
sarcosine

B: 312-84-5
D-Serine

C: 77421-34-2
L-β-hydroxy-N-methylvaline

D: 56-40-6
glycine

Conditions

Conditions	Yield
With hydrogenchloride at 100℃; for 18h; Further byproducts given;

...Expand

: 76110-01-5
luzopeptin C

A: 107-97-1
sarcosine

B: 312-84-5
D-Serine

C: 77421-33-1
3-hydroxy-6-methoxyquinoline-2-carboxylic acid

D: 56-40-6
glycine

Conditions

Conditions	Yield
With hydrogenchloride at 100℃; for 18h; Further byproducts given;

...Expand

: 74-90-8
hydrogen cyanide

carbon: carbon

A: 107-97-1
sarcosine

B: 56-40-6
glycine

C: 302-72-7
rac-Ala-OH

D: 107-95-9
3-amino propanoic acid

Conditions

Conditions	Yield
With ammonia; water at -196℃; Further byproducts given;	A 0.24 mmol B 3.0 mmol C 0.18 mmol D 0.17 mmol

...Expand

: 60-27-5
creatinine

: 107-97-1
sarcosine

Conditions

Conditions	Yield
Bei langandauernder Faeulnis;
With barium dihydroxide at 100℃; im Rohr;

: 79-11-8
chloroacetic acid

: 74-89-5
methylamine

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With water at 40℃;
With water

: 859960-32-0
N-methyl-N-phenylmethanesulfonyl-glycine

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With hydrogenchloride Hydrolysis.im geschlossenen Rohr;

: 98-98-6
2-Picolinic acid

: 107-97-1
sarcosine

: 34557-54-5
methane

: 7664-41-7
ammonia

: 7732-18-5
water

A: 107-97-1
sarcosine

B: 56-40-6
glycine

C: 2835-81-6
2-aminobutanoic acid

Conditions

Conditions	Yield
With hydrogen byproducts: dl-α-amino-butiric acid, dl-alanine, β-alanine; by electric spark discharge or electric discharge;

...Expand

: 1056469-56-7
C10H22N2O

A: 107-97-1
sarcosine

B (R)-2-heptylamine: 123-82-0, 6240-90-0, 7795-34-8, 44745-29-1
(R)-2-heptylamine

Conditions

Conditions	Yield
With novozyme 435; water at 70℃; for 147h; pH=7; aq. phosphate buffer; Enzymatic reaction;

C11H16N2O: C11H16N2O

A: 107-97-1
sarcosine

B: 3886-69-9
(R)-1-phenyl-ethyl-amine

Conditions

Conditions	Yield
With novozyme 435; water at 70℃; for 120h; pH=7; aq. phosphate buffer; Enzymatic reaction;

: (S)-3-Hydroxy-3-methyl-2-methylamino-butyric acid (R)-2-(carboxymethyl-methyl-carbamoyl)-2-[(3-hydroxy-6-methoxy-quinoline-2-carbonyl)-amino]-ethyl ester

A: 107-97-1
sarcosine

B: 77421-34-2
L-β-hydroxy-N-methylvaline

C: 77431-62-0
(R)-3-Hydroxy-2-[(3-hydroxy-6-methoxy-quinoline-2-carbonyl)-amino]-propionic acid

Conditions

Conditions	Yield
With water; hydroxide

...Expand

: 74-89-5
methylamine

C: C

A: 107-97-1
sarcosine

B: 600-21-5
N-methylalanine

C: 617-45-8
aspartic Acid

Conditions

Conditions	Yield
With ammonia Yield given. Further byproducts given. Yields of byproduct given;

...Expand

: 13256-22-9, 55332-66-6, 55332-68-8
N-nitrososarcosine

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With sodium azide; sulfuric acid; SC(NH2)2 In water; acetic acid at 25℃; Rate constant; other solvent; other catalysts;
With perchloric acid; ammonium sulfamate; sodium thiocyanide at 50℃; Rate constant; piperidinium perchlorate, 18h; transnitrosating studies;

: 74-89-5
methylamine

C: C

A: 107-97-1
sarcosine

B: 56-40-6
glycine

C: 302-72-7
rac-Ala-OH

D: 107-95-9
3-amino propanoic acid

Conditions

Conditions	Yield
With ammonia Yield given. Further byproducts given. Yields of byproduct given;

...Expand

: 56-40-6
glycine

A: 107-97-1
sarcosine

B: 5473-12-1
N-methylglycine methylester

C: 556-50-3
glycylglycine

D: 142-73-4
iminodiacetic acid

Conditions

Conditions	Yield
With 5%-palladium/activated carbon; hydrogen at 180℃; under 300.03 Torr; for 0.166667h;

...Expand

: 46376-16-3
2-(N-methylphenylsulfonamido)acetic acid

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With sulfuric acid at 125 - 130℃;

: 616-34-2
methoxycarbonylmethylamine

A: 34037-21-3
morpholine-2,5-dione

B: 107-97-1
sarcosine

C: 5473-12-1
N-methylglycine methylester

D: 6096-81-7
dimethyl iminodiacetate

E: 56-40-6
glycine

Conditions

Conditions	Yield
With 5%-palladium/activated carbon; hydrogen at 180℃; under 300.03 Torr; for 0.166667h;

...Expand

: 79760-89-7
C16H19N2O4P

A: 107-97-1
sarcosine

B: 701-64-4
phosphoric acid monophenyl ester

C: 106-49-0
p-toluidine

Conditions

Conditions	Yield
With hydrogenchloride In 1,4-dioxane for 0.0833333h;

...Expand

: cordyheptapeptides B

A: 107-97-1
sarcosine

B: 61-90-5
L-leucine

C: 2566-30-5
N-Methyl-L-phenylalanine

D: 147-85-3
L-proline

Conditions

Conditions	Yield
With hydrogenchloride at 110℃; for 15h; Further byproducts. Title compound not separated from byproducts.;

...Expand

: 77287-34-4, 77287-35-5, 60100-09-6
formamide

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With Canyon Diablo iron meteorites at 140℃; for 24h; Reagent/catalyst; Temperature;

: 58-08-2
3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With barium dihydroxide; water
With barium dihydroxide

: 5616-32-0
(methylamino)acetonitrile

: 107-97-1
sarcosine

Conditions

Conditions	Yield
With barium dihydroxide; water
With barium dihydroxide

: perthamide C

A: 107-97-1
sarcosine

B: 4144-02-9
O-methyl-L-threonine

C: 7423-92-9
o-hydroxyl-phenylalanine

D: 6734-41-4
cis-4-methyl-(S)-proline

Conditions

Conditions	Yield
With hydrogenchloride; water at 130℃;

...Expand

: 107-97-1
sarcosine

: 64-17-5
ethanol

: 52605-49-9
sarcosine ethyl ester hydrochloride

Conditions

Conditions	Yield
With thionyl chloride at 0 - 78℃;	100%
With hydrogenchloride	99%
With hydrogenchloride at 20℃; for 72h;	95%
With hydrogenchloride
With acetyl chloride for 3h; Reflux;

: 107-97-1
sarcosine

: 501-53-1
benzyl chloroformate

: 39608-31-6
N-(Benzyloxycarbonyl)sarcosine

Conditions

Conditions	Yield
With sodium carbonate In 1,4-dioxane; water at 20℃;	100%
With sodium carbonate In 1,4-dioxane; water 1.) 0 deg C, 1.5 h, 2.) room temperature, 11 h;	99%
With sodium hydroxide In water at 0 - 20℃; for 16h;	94%

: 67-56-1
methanol

: 107-97-1
sarcosine

: 13515-93-0
N-methylglycine methyl ester hydrochloride

Conditions

Conditions	Yield
With thionyl chloride for 6.5h; Cooling; Reflux; Inert atmosphere;	100%
With thionyl chloride at 55℃; for 2h;	92%
With thionyl chloride 1.) ice-salt bath, 20 min, 2.) room temperature, 2 h, 3.) reflux, 2 h;	90%

: 107-97-1
sarcosine

: 24424-99-5
di-tert-butyl dicarbonate

: 13734-36-6
N-(tert-butoxycarbonyl)sarcosine

Conditions

Conditions	Yield
With triethylamine In water for 6h;	100%
With triethylamine In water at 25℃; for 3h;	97%
With sodium hydroxide In 1,4-dioxane	95%

: 107-97-1
sarcosine

A: 50-00-0
formaldehyd

B: 124-38-9
carbon dioxide

C: 74-89-5
methylamine

Conditions

Conditions	Yield
With hydrogenchloride; sodium hydroxide; sodium perchlorate; chlorine at 24.9℃; Mechanism; Rate constant; Equilibrium constant; multistep reaction: 1.) water, 298 deg K, 2.) water, 298 deg K; reactions under var. conditions;	A 100% B n/a C n/a

...Expand

: 50-00-0
formaldehyd

: 107-97-1
sarcosine

: 552-89-6
2-nitro-benzaldehyde

: 365275-13-4
3-methyl-5-(2'-nitrophenyl)oxazolidine

Conditions

Conditions	Yield
In toluene for 1h; Heating;	100%
In benzene for 1h; Heating;	95%

...Expand

: 107-97-1
sarcosine

: (C20H10N4((C4H9)2C6H3)3(C6H4))(C10H2N2O4)(C6H4)(CHO)

: 557-34-6
zinc diacetate

: 99685-96-8, 161105-99-3, 161106-00-9, 111138-12-6, 133318-63-5, 134053-11-5, 134931-35-4, 134931-36-5, 139703-76-7, 145633-27-8, 175414-73-0, 175414-74-1, 175414-75-2, 175519-12-7, 175519-13-8, 175519-14-9, 175519-15-0, 136376-46-0, 144906-37-6, 144906-38-7, 151767-00-9, 152882-97-8, 152882-98-9, 152882-99-0, 153062-34-1, 154171-74-1, 154171-75-2, 154333-99-0, 154334-00-6, 154397-63-4, 154460-59-0, 199456-56-9, 108739-25-9, 120329-57-9, 120329-58-0
fullerene-C60

: 201872-65-3
[Zn(C20H8N4((C4H9)2C6H3)3(C6H4)(C10H2N2O4)(C6H4)(CH3NC2H3)C60)]

Conditions

Conditions	Yield
In toluene C60, C20H10N4((C4H9)2C6H3)3(C6H4)2(C10H2N2O4)(CHO), N-methylglycine (toluene) heated under N2 in dark for 6 h; cooled to 25°C, evapd. to dryness (reduced pressure); chromy. sepd., dissolved (CH3Cl), added Zn(OAc)2 in CH3OH, heated for 30 min; washed twice (H2O), dried (anhydrous Na2SO4), solvent evapd., chromy., reprecipitated from benzene-methanol;	100%

...Expand

: 50-00-0
formaldehyd

: 107-97-1
sarcosine

: (Z)-4-(2-ethoxybenzylidene)-2-phenyloxazol-5(4H)-one

: (5R*,9R*)-9-(2-ethoxyphenyl)-7-methyl-2-phenyl-3-oxa-1,7-diazaspiro[4.4]non-1-en-4-one

Conditions

Conditions	Yield
In benzene for 5h; Reflux; Dean-Stark; diastereoselective reaction;	100%

...Expand

: 107-97-1
sarcosine

: 56-53-1
diethylstilbestrol

: C18H20O2*C3H7NO2

Conditions

Conditions	Yield
In methanol at 20℃;	99.01%

: 67-56-1
methanol

: 107-97-1
sarcosine

: 5473-12-1
N-methylglycine methylester

Conditions

Conditions	Yield
With thionyl chloride at 0℃; for 3.5h;	99%
With thionyl chloride
(i) SOCl2, (ii) /BRN= 1098229/; Multistep reaction;
at 0 - 20℃; for 12h;

: 107-97-1
sarcosine

: 2-(Diethoxy-phosphoryl)-thioacetimidic acid methyl ester; hydriodide

: {[2-(Diethoxy-phosphoryl)-acetimidoyl]-methyl-amino}-acetic acid

Conditions

Conditions	Yield
With pyridine In dichloromethane at 260℃;	99%

: 941-69-5
N-phenyl-maleimide

: 73568-29-3
2-chloro-6-methoxyquinolin-3-carboxaldehyde

: 107-97-1
sarcosine

(3aR,6aS)-4-(6-Methoxy-2-oxo-1,2-dihydro-quinolin-3-yl)-5-methyl-2-phenyl-tetrahydro-pyrrolo[3,4-c]pyrrole-1,3-dione: (3aR,6aS)-4-(6-Methoxy-2-oxo-1,2-dihydro-quinolin-3-yl)-5-methyl-2-phenyl-tetrahydro-pyrrolo[3,4-c]pyrrole-1,3-dione

Conditions

Conditions	Yield
In xylene for 2h; Heating;	99%

...Expand

: 3612-20-2
1-phenylmethyl-4-piperidone

: 107-97-1
sarcosine

: 336191-70-9
2-[(1-benzyl-4-piperidyl)(methyl)amino]acetic acid

Conditions

Conditions	Yield
With triethanolamine; acetic acid; trifluoroacetic acid In 1,2-dichloro-ethane	99%

: 50-00-0
formaldehyd

: 107-97-1
sarcosine

: 117133-77-4
(E)-methyl-3-(benzo[d][1,3]dioxol-5-yl)-2-cyanoacrylate

: methyl (3RS,4RS)-4-(1,3-benzodioxol-5-yl)-3-cyano-1-methylpyrrolidine-3-carboxylate

Conditions

Conditions	Yield
In toluene for 1.33333h; Reflux; stereospecific reaction;	99%

...Expand

: 50-00-0
formaldehyd

: 107-97-1
sarcosine

: 14479-58-4
methyl (E)- 2-cyano-3-(4-methoxyphenyl)prop-2-enoate

: methyl (3RS,4RS)-3-cyano-4-(4-methoxyphenyl)-1-methylpyrrolidine-3-carboxylate

Conditions

Conditions	Yield
In toluene for 1.25h; Reflux; stereospecific reaction;	99%

...Expand

: 107-97-1
sarcosine

: 912676-30-3
α-naphthyl isoselenocyanate

: 1310370-46-7
1-methyl-3-(1-naphthyl)-2-selenoxohydantoin

Conditions

Conditions	Yield
In 1,4-dioxane at 100℃; for 3.5h;	99%

: 107-97-1
sarcosine

: 1217-89-6
1-benzylisatin

: 13672-24-7
ethyl (2E)-(1-benzyl-2-oxo-1,2-dihydro-3H-indol-3-ylidene)acetate

: C36H33N3O4

Conditions

Conditions	Yield
In ethanol at 20℃; for 2h; diastereoselective reaction;	99%

...Expand

: 107-97-1
sarcosine

: 1217-89-6
1-benzylisatin

: (3S*,5’S*)-1,1’’-dibenzyl-3’-methyldispiro[indoline-3,4’-oxazolidine-5’,3’’-indoline]-2,2’’-dione

Conditions

Conditions	Yield
In dimethyl sulfoxide at 20℃; for 4h; Green chemistry; diastereoselective reaction;	99%
With 3-nitro-2-(trifluoromethyl)-2H-chromene In isopropyl alcohol at 55 - 60℃; for 5h;	43%

: 50-00-0
formaldehyd

: 72167-88-5
4-phenylsulphonyl-2H-chromene-2-one

: 107-97-1
sarcosine

: 127599-33-1
1,3-dihydro-2-methyl-pyrrolo(3,4-c)chromene-4-one

Conditions

Conditions	Yield
In benzene for 3h; Heating;	98%

...Expand

: 50-00-0
formaldehyd

: 107-97-1
sarcosine

: 99-61-6
3-nitro-benzaldehyde

: 3-methyl-5-(3-nitro-phenyl)-oxazolidine

Conditions

Conditions	Yield
In benzene for 1h; Heating;	98%

...Expand

: (3E,5E)-1-methyl-3,5-bis(4-fluorobenzylidene)piperidin-4-one

: 107-97-1
sarcosine

: 82-86-0
acenaphthene quinone

: 1-methyl-4-(4-fluorophenyl)pyrrole(spiro[2.2'']acenaphthene-1''-one)-spiro[3.3']-5'-(4-fluorophenylmethylidene)-1'-methyltetrahydro-4'(1'H)-pyridinone

Conditions

Conditions	Yield
In methanol for 1h; Reflux; stereoselective reaction;	98%
In methanol for 1h; Heating;	97%

...Expand

: (3E,5E)-3,5-bis(2-chlorobenzylidene)-1-methylpiperidin-4-one

: 107-97-1
sarcosine

: 82-86-0
acenaphthene quinone

: 1-methyl-4-(2-chlorophenyl)pyrrole(spiro[2.2'']acenaphthene-1''-one)-spiro[3.3']-5'-(2-chlorophenylmethylidene)-1'-methyltetrahydro-4'(1'H)-pyridinone

Conditions

Conditions	Yield
In methanol for 1h; Heating;	98%

...Expand

: C8H9NOC12H8F2

: 107-97-1
sarcosine

: 82-86-0
acenaphthene quinone

: 1-methyl-4-(3-fluorophenyl)pyrrole(spiro[2.2'']acenaphthene-1''-one)-spiro[3.3']-5'-(3-fluorophenylmethylidene)-1'-methyltetrahydro-4'(1'H)-pyridinone

Conditions

Conditions	Yield
In methanol for 1h; Reflux; stereoselective reaction;	98%
In methanol for 1h; Heating;	96%

...Expand

: 107-97-1
sarcosine

: 4369-12-4
(E)-1-methyl-3,5-bis(4-methoxybenzylidene)-4-piperidone

: 82-86-0
acenaphthene quinone

: 1-methyl-4-(4-methoxyphenyl)pyrrole(spiro[2.2'']acenaphthene-1''-one)-spiro[3.3']-5'-(4-methoxyphenylmethylidene)-1'-methyltetrahydro-4'(1'H)-pyridinone

Conditions

Conditions	Yield
In methanol for 1h; Heating;	98%

...Expand

: 50-00-0
formaldehyd

: 762173-03-5
2-(4-fluorophenyl)-3-(2-methylsulfanylpyrimidin-4-yl)imidazo[1,2-a]pyridine-7-carbaldehyde

: 107-97-1
sarcosine

: 762173-04-6
2-(4-fluorophenyl)-7-(3-methyloxazolidin-5-yl)-3-(methylsulfanylpyrimidin-4-yl)imidazo[1,2-a]pyridine

Conditions

Conditions	Yield
In toluene for 12h; Heating;	98%

...Expand

: 107-97-1
sarcosine

: 14223-48-4
p-chlorophenyl isoselenocyanate

: 1310370-38-7
3-(p-chlorophenyl)-1-methyl-2-selenoxohydantoin

Conditions

Conditions	Yield
In 1,4-dioxane at 100℃; for 5h;	98%

: 107-97-1
sarcosine

: 1353546-25-4
C21H17NO

: 17630-76-1
5-chloroindole 2,3-dione

: C31H26ClN3O2

Conditions

Conditions	Yield
In 1,4-dioxane; methanol Reflux; stereoselective reaction;	98%

...Expand

: 107-97-1
sarcosine

: 1353546-31-2
(E)-2-[4-chlorobenzylidene]-3,4-dihydro-1(2H)-acridinone

: 91-56-5
indole-2,3-dione

: C30H24ClN3O2

Conditions

Conditions	Yield
In 1,4-dioxane; methanol for 6h; Reflux; stereoselective reaction;	98%

...Expand

: 107-97-1
sarcosine

: 25554-84-1
2-(ethoxycarbonothioylthio)acetic acid

: 59857-32-8
N-(ethoxycarbonothioyl)-N-methylglycine

Conditions

Conditions	Yield
With sodium hydroxide In water at 20℃; for 48h;	98%
With sodium hydroxide In water at 25℃; for 72h;
In water
With sodium hydroxide In water

Sarcosine History

Sarcosine was first isolated and named by the German chemist Justus von Liebig in 1847, while Jacob Volhard first synthesized it in 1862.

Sarcosine Specification

The Sarcosine is an amino acid intermediate in the metabolism of choline. The IUPAC name of this chemical is 2-(methylamino)acetic acid. With the CAS registry number 107-97-1, it is also named as Glycine, N-methyl-. The product's categories are amino acids series;sarcosine [sar];amino acids. It is white crystalline powder with a sweetish taste. And it is soluble in water, ethanol and dilute ethanol, insoluble in ether. Additionally, people should keep this chemical in cool and dry place and keep away from fire, heat and water.

The other characteristics of this product can be summarized as: (1)ACD/LogP: -0.79; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -3.29; (4)ACD/LogD (pH 7.4): -3.29; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 3; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 2; (12)Index of Refraction: 1.431; (13)Molar Refractivity: 21.1 cm³; (14)Molar Volume: 81.4 cm³; (15)Polarizability: 8.36×10^-24 cm³; (16)Surface Tension: 37.1 dyne/cm; (17)Enthalpy of Vaporization: 47.54 kJ/mol; (18)Vapour Pressure: 0.184 mmHg at 25°C; (19)Rotatable Bond Count: 2; (20)Exact Mass: 89.047678; (21)MonoIsotopic Mass: 89.047678; (22)Topological Polar Surface Area: 49.3; (23)Heavy Atom Count: 6; (24)Complexity: 52.8.

Preparation of Sarcosine: Digesting the bark of Quillaia saponaria by hot water or aqueous ethanol, then using ether or acetone to make it precipitation. Finally, we can get the product by re-crystallization and refining.

Uses of Sarcosine: It is used as biochemical reagent, dye stabilizer, daily chemical, amino acid surfactants, health drugs fatigue recovery agent and so on. It also can react with ethanol to get N-methyl-glycine ethyl ester. This reaction needs reagent aqueous HCl.

When you are using this chemical, please be cautious about it as the following:
It is irritating to eyes, respiratory system and skin, so people should avoid contact with skin and eyes. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If you want to contact this product, you must wear suitable protective clothing.

People can use the following data to convert to the molecule structure.
1. SMILES:O=C(O)CNC
2. InChI:InChI=1/C3H7NO2/c1-4-2-3(5)6/h4H,2H2,1H3,(H,5,6)
3. InChIKey:FSYKKLYZXJSNPZ-UHFFFAOYAL

Product Name

Sarcosine

Synthetic route

Sarcosine History

Sarcosine Specification

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