Product Name

  • Name

    DL-METHIONINE METHYLSULFONIUM CHLORIDE

  • EINECS 222-484-4
  • CAS No. 3493-12-7
  • Article Data2
  • CAS DataBase
  • Density
  • Solubility
  • Melting Point 139-140 °C (dec.)
  • Formula C6H14 NO2 S.Cl
  • Boiling Point
  • Molecular Weight 199.702
  • Flash Point
  • Transport Information
  • Appearance
  • Safety 24/25
  • Risk Codes
  • Molecular Structure Molecular Structure of 3493-12-7 (DL-METHIONINE METHYLSULFONIUM CHLORIDE)
  • Hazard Symbols
  • Synonyms Sulfonium,(3-amino-3-carboxypropyl)dimethyl-, chloride (9CI);Sulfonium,(3-amino-3-carboxypropyl)dimethyl-, chloride, (?à)-;Sulfonium, (3-amino-3-carboxypropyl)dimethyl-,chloride, DL- (8CI);(3-Amino-3-carboxypropyl)dimethylsulfonium chloride;DL-Methionine methylsulfonium chloride;dl-Methionine methylsulphoniumchloride;g-Dimethylsulfonium-a-aminobutyric acid chloride;Vitamin U(DL METHIONINE S METHYLSULFONIUM CHLORIDE);
  • PSA 88.62000
  • LogP -2.62940

Synthetic route

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

glycine
56-40-6

glycine

zinc(II) oxide

zinc(II) oxide

(diaquachloro-S-methylmethioniato)(glycinato)zinc

(diaquachloro-S-methylmethioniato)(glycinato)zinc

Conditions
ConditionsYield
In water reaction of ZnO with ligands in H2O (equimolar amounts); elem. anal.;96%
DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

aspartic Acid
617-45-8

aspartic Acid

zinc(II) oxide

zinc(II) oxide

(diaquachloro-S-methylmethioninato)(asparaginato)-O,O'-zinc

(diaquachloro-S-methylmethioninato)(asparaginato)-O,O'-zinc

Conditions
ConditionsYield
In ethanol reaction of ZnO with ligands in H2O (equimolar amounts); elem. anal.;96%
DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

rac-Ala-OH
302-72-7

rac-Ala-OH

zinc(II) oxide

zinc(II) oxide

(aquachloro-S-methylmethioniato)(alaninato)zinc

(aquachloro-S-methylmethioniato)(alaninato)zinc

Conditions
ConditionsYield
In water reaction of ZnO with ligands in H2O (equimolar amounts); elem. anal.;95%
Glutamic acid
617-65-2

Glutamic acid

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

zinc(II) oxide

zinc(II) oxide

(aquachloro-S-methylmethionato)(glutaminato)-O,O'-zinc
132032-38-3

(aquachloro-S-methylmethionato)(glutaminato)-O,O'-zinc

Conditions
ConditionsYield
In water reaction of ZnO with ligands in H2O (equimolar amounts); elem. anal.;93%
chloride
16887-00-6

chloride

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

chloroperoxidase

chloroperoxidase

A

methyl bromide
74-83-9

methyl bromide

B

methylene chloride
74-87-3

methylene chloride

C

methyl iodide
74-88-4

methyl iodide

Conditions
ConditionsYield
With sea salt; dihydrogen peroxide; potassium carbonate In phosphate buffer Methylation;
bromide
10097-32-2

bromide

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

chloroperoxidase

chloroperoxidase

A

methyl bromide
74-83-9

methyl bromide

B

methyl iodide
74-88-4

methyl iodide

Conditions
ConditionsYield
With sea salt; dihydrogen peroxide; potassium carbonate In phosphate buffer Methylation;
iodide
14362-44-8

iodide

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

chloroperoxidase

chloroperoxidase

A

methyl bromide
74-83-9

methyl bromide

B

methyl iodide
74-88-4

methyl iodide

Conditions
ConditionsYield
With sea salt; dihydrogen peroxide; potassium carbonate In phosphate buffer Methylation;
DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

A

(3-carboxy-3-chloro-propyl)-dimethyl sulfonium

(3-carboxy-3-chloro-propyl)-dimethyl sulfonium

B

<3-carboxy-3-hydroxy-propyl>-dimethyl sulfonium

<3-carboxy-3-hydroxy-propyl>-dimethyl sulfonium

Conditions
ConditionsYield
With hydrogenchloride; sodium nitrite
cobalt(III) hydroxide

cobalt(III) hydroxide

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Co{(CH3)2S(Cl)(CH2)2CH(NH2)COO}3*2H2O

Co{(CH3)2S(Cl)(CH2)2CH(NH2)COO}3*2H2O

Conditions
ConditionsYield
In not given room temp.;
cobalt(III) hydroxide

cobalt(III) hydroxide

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Co{(CH3)2S(Cl)(CH2)2CH(NH2)COO}3*4H2O

Co{(CH3)2S(Cl)(CH2)2CH(NH2)COO}3*4H2O

Conditions
ConditionsYield
In not given heating (67-70°C, 3 h);
DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

cobalt(II) chloride
7646-79-9

cobalt(II) chloride

A

2(CH3)2S(CH2)2CH(NH3)COO(1+)*CoCl4(2-)={(CH3)2S(CH2)2CH(NH3)COO}2CoCl4

2(CH3)2S(CH2)2CH(NH3)COO(1+)*CoCl4(2-)={(CH3)2S(CH2)2CH(NH3)COO}2CoCl4

B

(CH3)2S(CH2)2CH(NH3)COO(1+)*CoCl3(1-)={(CH3)2S(CH2)2CH(NH3)COO}CoCl3

(CH3)2S(CH2)2CH(NH3)COO(1+)*CoCl3(1-)={(CH3)2S(CH2)2CH(NH3)COO}CoCl3

Conditions
ConditionsYield
In acetone
nickel(II) chloride hexahydrate

nickel(II) chloride hexahydrate

Glutamic acid
617-65-2

Glutamic acid

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

{NiCl3(H2O)3}(1-)*(CH3)2SC3H5NH2COOH(1+)*COOHCHNH2C2H4COOH*8H2O={NiCl3(H2O)3}(CH3)2SC3H5NH2COOH(COOHCHNH2C2H4COOH)*8H2O

{NiCl3(H2O)3}(1-)*(CH3)2SC3H5NH2COOH(1+)*COOHCHNH2C2H4COOH*8H2O={NiCl3(H2O)3}(CH3)2SC3H5NH2COOH(COOHCHNH2C2H4COOH)*8H2O

Conditions
ConditionsYield
In ethanol addn. of an equimolar quantity of NiCl2*6H2O to satd. solns. of the ligands in ethanol; purifn. with ethanol, isolation from the mother soln. with acetone, elem. anal.;
copper(II) choride dihydrate

copper(II) choride dihydrate

Glutamic acid
617-65-2

Glutamic acid

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Cu(2+)*2Cl(1-)*HOOCC2H4CH(NH2)COO(1-)*H2O*HO2CCH(NH2)CH2CH2S(CH3)2(1+)={CuCl2(C5H8O4N)(H2O)}{HO2CCH(NH2)CH2CH2S(CH3)2}

Cu(2+)*2Cl(1-)*HOOCC2H4CH(NH2)COO(1-)*H2O*HO2CCH(NH2)CH2CH2S(CH3)2(1+)={CuCl2(C5H8O4N)(H2O)}{HO2CCH(NH2)CH2CH2S(CH3)2}

Conditions
ConditionsYield
In ethanol; water addn. of Cu-salt in EtOH to saturated aq. soln. of ligands, stirred until no further decolourisation of the supernatant liquid; sepn. of the mother-liquor, residue treated two or three times with EtOH and with acetone until the organic solvent gave negative test for Cl(1-), powdered product washed three times with ether; elem. anal.;
nickel(II) carbonate
719261-06-0

nickel(II) carbonate

Glutamic acid
617-65-2

Glutamic acid

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Ni((CH3)2SCH2CH2CH(NH2)COO)(COOCH(NH2)(CH2)2COOH)(H2O)2(1+)*Cl(1-)=Ni((CH3)2S(Cl)C3H5(NH2)COO)(COOCH(NH2)C2H4COOH)*2H2O

Ni((CH3)2SCH2CH2CH(NH2)COO)(COOCH(NH2)(CH2)2COOH)(H2O)2(1+)*Cl(1-)=Ni((CH3)2S(Cl)C3H5(NH2)COO)(COOCH(NH2)C2H4COOH)*2H2O

Conditions
ConditionsYield
In water addn. of basic NiCO3 to equimolar quantities of the ligands dissolved in water; filtration, salting-out by repeated treating with acetone, elem. anal.;
nickel(II) chloride hexahydrate

nickel(II) chloride hexahydrate

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

glycine
56-40-6

glycine

{NiCl3(H2O)3}(1-)*(CH3)2SCH2CH2CH(NH2)COOH(1+)*CH2(NH2)COOH*2H2O={NiCl3(H2O)3}((CH3)2SC3H5(NH2)COOH)(CH2(NH2)COOH)*2H2O

{NiCl3(H2O)3}(1-)*(CH3)2SCH2CH2CH(NH2)COOH(1+)*CH2(NH2)COOH*2H2O={NiCl3(H2O)3}((CH3)2SC3H5(NH2)COOH)(CH2(NH2)COOH)*2H2O

Conditions
ConditionsYield
In ethanol addn. of an equimolar quantity of NiCl2*6H2O to satd. solns. of the ligands in ethanol; purifn. with ethanol, isolation from the mother soln. with acetone, elem. anal.;
nickel(II) chloride hexahydrate

nickel(II) chloride hexahydrate

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

aspartic Acid
617-45-8

aspartic Acid

{NiCl3(H2O)3}(1-)*(CH3)2SC3H5NH2COOH(1+)*COOHCHNH2CH2COOH*5H2O={NiCl3(H2O)3}(CH3)2SC3H5NH2COOH(COOHCHNH2CH2COOH)*5H2O

{NiCl3(H2O)3}(1-)*(CH3)2SC3H5NH2COOH(1+)*COOHCHNH2CH2COOH*5H2O={NiCl3(H2O)3}(CH3)2SC3H5NH2COOH(COOHCHNH2CH2COOH)*5H2O

Conditions
ConditionsYield
In ethanol addn. of an equimolar quantity of NiCl2*6H2O to satd. solns. of the ligands in ethanol; purifn. with ethanol, isolation from the mother soln. with acetone, elem. anal.;
nickel(II) chloride hexahydrate

nickel(II) chloride hexahydrate

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

rac-Ala-OH
302-72-7

rac-Ala-OH

{NiCl3(H2O)3}(1-)*(CH3)2SCH2CH2CH(NH2)COOH(1+)*CH3CH(NH2)COOH*3H2O={NiCl3(H2O)3}(CH3)2SC3H5(NH2)COOH(CH3CHNH2COOH)*3H2O

{NiCl3(H2O)3}(1-)*(CH3)2SCH2CH2CH(NH2)COOH(1+)*CH3CH(NH2)COOH*3H2O={NiCl3(H2O)3}(CH3)2SC3H5(NH2)COOH(CH3CHNH2COOH)*3H2O

Conditions
ConditionsYield
In ethanol addn. of an equimolar quantity of NiCl2*6H2O to satd. solns. of the ligands in ethanol; purifn. with ethanol, isolation from the mother soln. with acetone, elem. anal.;
copper(II) choride dihydrate

copper(II) choride dihydrate

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

glycine
56-40-6

glycine

CuCl2(H2NCH2COO)(H2O)2(1-)*HO2CCH(NH2)CH2CH2S(CH3)2(1+)*2H2O={CuCl2(H2NCH2COO)(H2O)2}(HO2CCH(NH2)CH2CH2S(CH3)2)*2H2O

CuCl2(H2NCH2COO)(H2O)2(1-)*HO2CCH(NH2)CH2CH2S(CH3)2(1+)*2H2O={CuCl2(H2NCH2COO)(H2O)2}(HO2CCH(NH2)CH2CH2S(CH3)2)*2H2O

Conditions
ConditionsYield
In ethanol; water addn. of Cu-salt in EtOH to saturated aq. soln. of ligands, stirred until no further decolourisation of the supernatant liquid; sepn. of the mother-liquor, residue treated two or three times with EtOH and with acetone until the organic solvent gave negative test for Cl(1-), powdered product washed three times with ether; elem. anal.;
copper(II) choride dihydrate

copper(II) choride dihydrate

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

aspartic Acid
617-45-8

aspartic Acid

CuCl2(HOOCCH2CHNH2COO)(H2O)2(1-)*HO2CCHNH2CH2CH2S(CH3)2(1+)={CuCl2(HOOCCH2CHNH2COO)(H2O)2}{HO2CCHNH2CH2CH2S(CH3)2}

CuCl2(HOOCCH2CHNH2COO)(H2O)2(1-)*HO2CCHNH2CH2CH2S(CH3)2(1+)={CuCl2(HOOCCH2CHNH2COO)(H2O)2}{HO2CCHNH2CH2CH2S(CH3)2}

Conditions
ConditionsYield
In ethanol; water addn. of Cu-salt in EtOH to saturated aq. soln. of ligands, stirred until no further decolourisation of the supernatant liquid; sepn. of the mother-liquor, residue treated two or three times with EtOH and with acetone until the organic solvent gave negative test for Cl(1-), powdered product washed three times with ether; elem. anal.;
copper(II) choride dihydrate

copper(II) choride dihydrate

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

rac-Ala-OH
302-72-7

rac-Ala-OH

Cu(2+)*2Cl(1-)*CH3CH(NH2)COO(1-)*H2O*HO2CCH(NH2)CH2CH2S(CH3)2(1+)={CuCl2(CH3CH(NH2)COO)(H2O)}(HO2CCH(NH2)CH2CH2S(CH3)2)

Cu(2+)*2Cl(1-)*CH3CH(NH2)COO(1-)*H2O*HO2CCH(NH2)CH2CH2S(CH3)2(1+)={CuCl2(CH3CH(NH2)COO)(H2O)}(HO2CCH(NH2)CH2CH2S(CH3)2)

Conditions
ConditionsYield
In ethanol; water addn. of Cu-salt in EtOH to saturated aq. soln. of ligands, stirred until no further decolourisation of the supernatant liquid; sepn. of the mother-liquor, residue treated two or three times with EtOH and with acetone until the organic solvent gave negative test for Cl(1-), powdered product washed three times with ether; elem. anal.;
iron(III) chloride hexahydrate

iron(III) chloride hexahydrate

S-methyl-L-cysteine
1187-84-4

S-methyl-L-cysteine

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Fe(3+)*O2CCH(NH2)CH2CH2S(CH3)2*Cl(1-)*2O2CCH(NH2)CH2SCH3(1-)*3H2O=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)(O2CCH(NH2)CH2SCH3)2*3H2O

Fe(3+)*O2CCH(NH2)CH2CH2S(CH3)2*Cl(1-)*2O2CCH(NH2)CH2SCH3(1-)*3H2O=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)(O2CCH(NH2)CH2SCH3)2*3H2O

Conditions
ConditionsYield
In water addn. of FeCl3*6H2O to a mixt. of vitamin U and S-methyl-L-cysteine in water (molar ratio 1:1:2), addn. of LiCO3 in small portions, liberation of CO2; complex isolated from the soln. by addn. of a 1:1 mixt. of acetone and alcohol, oily ppt., treated with acetone to give a powder, washed with ether; elem. anal.;
α-ketoglutaric acid
328-50-7

α-ketoglutaric acid

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

zinc(II) oxide

zinc(II) oxide

Zn(O2CC(O)CH2CH2CO2H)(O2CCH(NH2)(CH2)2S(CH3)2)(H2O)(1+)*Cl(1-)=Zn(O2CC(O)CH2CH2CO2H)(O2CCH(NH2)(CH2)2S(CH3)2Cl)*H2O

Zn(O2CC(O)CH2CH2CO2H)(O2CCH(NH2)(CH2)2S(CH3)2)(H2O)(1+)*Cl(1-)=Zn(O2CC(O)CH2CH2CO2H)(O2CCH(NH2)(CH2)2S(CH3)2Cl)*H2O

Conditions
ConditionsYield
In water react. with ZnO with stirring until dissolution of the ZnO; salting-out with acetone, elem. anal.;
nickel(II) carbonate
719261-06-0

nickel(II) carbonate

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

glycine
56-40-6

glycine

Ni((CH3)2SCH2CH2CH(NH2)COO)(CH2(NH2)COO)(1+)(H2O)2*Cl(1-)=Ni((CH3)2S(Cl)CH2CH2CH(NH2)COO)(CH2(NH2)COO)*2H2O

Ni((CH3)2SCH2CH2CH(NH2)COO)(CH2(NH2)COO)(1+)(H2O)2*Cl(1-)=Ni((CH3)2S(Cl)CH2CH2CH(NH2)COO)(CH2(NH2)COO)*2H2O

Conditions
ConditionsYield
In water addn. of basic NiCO3 to equimolar quantities of the ligands dissolved in water; filtration, salting-out by repeated treating with acetone, elem. anal.;
nickel(II) carbonate
719261-06-0

nickel(II) carbonate

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

aspartic Acid
617-45-8

aspartic Acid

Ni((CH3)2SCH2CH2CH(NH2)COO)(COOCH(NH3)CH2COO)(H2O)2(1+)*Cl(1-)*H2O=Ni((CH3)2S(Cl)C3H5(NH2)COO)(COOCH(NH3)CH2COO)*3H2O

Ni((CH3)2SCH2CH2CH(NH2)COO)(COOCH(NH3)CH2COO)(H2O)2(1+)*Cl(1-)*H2O=Ni((CH3)2S(Cl)C3H5(NH2)COO)(COOCH(NH3)CH2COO)*3H2O

Conditions
ConditionsYield
In water addn. of basic NiCO3 to equimolar quantities of the ligands dissolved in water; filtration, salting-out by repeated treating with acetone, elem. anal.;
ferric hydroxide

ferric hydroxide

S-methyl-L-cysteine
1187-84-4

S-methyl-L-cysteine

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Fe(3+)*2O2CCHNH2CH2CH2S(CH3)2*2Cl(1-)*O2CCH(NH2)CH2SCH3(1-)*2H2O=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)2(O2CCH(NH2)CH2SCH3)*2H2O

Fe(3+)*2O2CCHNH2CH2CH2S(CH3)2*2Cl(1-)*O2CCH(NH2)CH2SCH3(1-)*2H2O=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)2(O2CCH(NH2)CH2SCH3)*2H2O

Conditions
ConditionsYield
In water addn. of vitamin U and S-methyl-L-cysteine to metal hydroxide in water (molar ratio 2:1:1), stirred to give a soln.; addn. of acetone; elem. anal.;
ferric hydroxide

ferric hydroxide

S-methyl-L-cysteine
1187-84-4

S-methyl-L-cysteine

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Fe(3+)*O2CCH(NH2)CH2CH2S(CH3)2*Cl(1-)*2O2CCH(NH2)CH2SCH3(1-)=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)(O2CCH(NH2)CH2SCH3)2

Fe(3+)*O2CCH(NH2)CH2CH2S(CH3)2*Cl(1-)*2O2CCH(NH2)CH2SCH3(1-)=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)(O2CCH(NH2)CH2SCH3)2

Conditions
ConditionsYield
In water addn. of Fe(OH)3 to a mixt. of vitamin U and S-methyl-L-cysteine in water (molar ratio 1:1:2); complex isolated from the soln. by addn. of a 1:1 mixt. of acetone and alcohol, oily ppt., treated with acetone to give a powder, washed with ether; elem. anal.;
ferric hydroxide

ferric hydroxide

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Fe(3+)*(O2CCH(NH2)CH2CH2S(CH3)2Cl)(1-)*2(O2CCH(NH2)CH2SH)(1-)*4H2O=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)(O2CCH(NH2)CH2SH)2*4H2O

Fe(3+)*(O2CCH(NH2)CH2CH2S(CH3)2Cl)(1-)*2(O2CCH(NH2)CH2SH)(1-)*4H2O=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)(O2CCH(NH2)CH2SH)2*4H2O

Conditions
ConditionsYield
In water addn. of vitamin U and cysteine to metal hydroxide in water (molar ratio 1:2:1), stirred (6 d), loose ppt.; sepn. of the ppt. from the supernatant liquid, treated with acetone, when it became viscous, treated with acetone to give a powder, washed with ether; elem. anal.;
ferric hydroxide

ferric hydroxide

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Fe(O2CCH(NH2)CH2CH2S(CH3)2)2(O2CCH(NH3)CH2S)(2+)*2Cl(1-)*3H2O=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)2(O2CCH(NH3)CH2S)*3H2O

Fe(O2CCH(NH2)CH2CH2S(CH3)2)2(O2CCH(NH3)CH2S)(2+)*2Cl(1-)*3H2O=Fe(O2CCH(NH2)CH2CH2S(CH3)2Cl)2(O2CCH(NH3)CH2S)*3H2O

Conditions
ConditionsYield
In water addn. of vitamin U and cysteine to metal hydroxide in water (molar ratio 2:1:1), stirred (6 d), loose ppt.; sepn. of the ppt. from the supernatant liquid, treated with acetone, when it became viscous, treated with acetone to give a powder, washed with ether; elem. anal.;
chromium(III) hydroxide

chromium(III) hydroxide

DL-methionine-S-methylsulfonium chloride
3493-12-7

DL-methionine-S-methylsulfonium chloride

Cr(O2CCH(NH2)CH2CH2S(CH3)2)(O2CCH(NH2)CH2S)(H2O)(1+)*Cl(1-)*H2O=Cr(O2CCH(NH2)CH2CH2S(CH3)2Cl)(O2CCH(NH2)CH2S)(H2O)*H2O

Cr(O2CCH(NH2)CH2CH2S(CH3)2)(O2CCH(NH2)CH2S)(H2O)(1+)*Cl(1-)*H2O=Cr(O2CCH(NH2)CH2CH2S(CH3)2Cl)(O2CCH(NH2)CH2S)(H2O)*H2O

Conditions
ConditionsYield
In water addn. of vitamin U and cysteine to metal hydroxide in water (molar ratio 1:1:1), stirred (4 d), pptn.; treatment with acetone; elem. anal.;

DL-Methionine methylsulfonium chloride Specification

The Sulfonium,(3-amino-3-carboxypropyl)dimethyl-, chloride (1:1), with the cas registry number 3493-12-7, has the IUPAC name of (3-amino-4-hydroxy-4-oxobutyl)-dimethylsulfanium chloride. And its product categories are including Iodonium Sulfonium & Oxonium Compounds; Sulfonium Compounds.

The characteristics of this kind of chemical are as follows: (1)#H bond acceptors: 3; (2)#H bond donors: 3; (3)#Freely Rotating Bonds: 5; (4)Polar Surface Area: 63.32; (5)Exact Mass: 199.043377; (6)MonoIsotopic Mass: 199.043377; (7)Topological Polar Surface Area: 64.3; (8)Heavy Atom Count: 11; (9)Complexity: 116; (10)Undefined Atom StereoCenter Count: 1; (11)Covalently-Bonded Unit Count: 2.

Additionally, the following datas could be converted into the molecular structure:
(1)Canonical SMILES: C[S+](C)CCC(C(=O)O)N.[Cl-]
(2)InChI: InChI=1S/C6H13NO2S.ClH/c1-10(2)4-3-5(7)6(8)9;/h5H,3-4,7H2,1-2H3;1H
(3)InChIKey: MYGVPKMVGSXPCQ-UHFFFAOYSA-N 

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