Product Name

  • Name

    1-Methylpyridinium chloride

  • EINECS 231-658-9
  • CAS No. 7680-73-1
  • Article Data13
  • CAS DataBase
  • Density
  • Solubility
  • Melting Point 144 °C
  • Formula C6H8 N . Cl
  • Boiling Point
  • Molecular Weight 129.589
  • Flash Point
  • Transport Information
  • Appearance
  • Safety Poison by ingestion, subcutaneous, and intraperitoneal routes. When heated to decomposition it emits toxic fumes of Cl and NOx.
  • Risk Codes 20/21/22-36/37/38
  • Molecular Structure Molecular Structure of 7680-73-1 (1-Methylpyridinium chloride)
  • Hazard Symbols
  • Synonyms 1-Methylpyridiniumchloride (6CI,7CI); Pyridinium, 1-methyl-, chloride (8CI,9CI); Methylpyridiniumchloride; N-Methylpyridinium chloride
  • PSA 3.88000
  • LogP -2.48490

Synthetic route

N-methylpyridinium p-toluenesulfonate
38542-71-1

N-methylpyridinium p-toluenesulfonate

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
With Dowex 1-X8 (Cl) 100-200 mesh standard grade resin In water Inert atmosphere;97%
pyridine
110-86-1

pyridine

N,N-dimethoxyamine
88470-26-2

N,N-dimethoxyamine

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
With tert-butylhypochlorite In diethyl ether at -78 - -8℃;21%
pyridine
110-86-1

pyridine

methylene chloride
74-87-3

methylene chloride

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
Thermodynamic data; Heating;
In ethanol at 80℃; under 3750.38 Torr; for 6h; Temperature; Pressure;
With benzene
pyridine hydrochloride
628-13-7

pyridine hydrochloride

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
With methanol at 160℃;
With formaldehyd at 200℃;
pyridine
110-86-1

pyridine

2-methoxy-1,3-dioxane
17230-31-8

2-methoxy-1,3-dioxane

A

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

B

allyl alcohol
107-18-6

allyl alcohol

Conditions
ConditionsYield
With di-tert-butyl peroxide In tetrachloromethane at 20℃; Irradiation; posiible mechanism discussed; relative rates of hydrogen abstraction were determined both by EPR technique (Me3COOCMe3) and by GC (this conditions); stereoelectronic effects in this process was compared for a series of 1,3-dioxanes;
N-methyl-3-dehydropyridinium ylid

N-methyl-3-dehydropyridinium ylid

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
With hydrogenchloride In methanol at -196.15℃; protonation;0.19 mmol
hydrogenchloride
7647-01-0

hydrogenchloride

5-(2,4-dinitro-anilino)-penta-2,4-dienal-methylimine

5-(2,4-dinitro-anilino)-penta-2,4-dienal-methylimine

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

pyridine
110-86-1

pyridine

hydrogen chloride

hydrogen chloride

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
With methanol
N-Methylpyrrole
96-54-8

N-Methylpyrrole

pyrographite
7440-44-0

pyrographite

A

3-iodo-N-methylpyridinium chloride
54560-59-7

3-iodo-N-methylpyridinium chloride

B

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
Stage #1: N-Methylpyrrole; pyrographite With methyl iodide at -196.15℃; Iodination; addition; electric arc;
Stage #2: With hydrogenchloride In methanol at -196.15℃; acidolysis;
N-Methylpyrrole
96-54-8

N-Methylpyrrole

pyrographite
7440-44-0

pyrographite

A

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

B

3-chloro-N-methylpyridinium chloride

3-chloro-N-methylpyridinium chloride

Conditions
ConditionsYield
Stage #1: N-Methylpyrrole; pyrographite With methylene chloride at -196.15℃; Chlorination; addition; electric arc;
Stage #2: With hydrogenchloride In methanol at -196.15℃; acidolysis;
N-Methylpyrrole
96-54-8

N-Methylpyrrole

pyrographite
7440-44-0

pyrographite

A

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

B

3-chloro-N-methylpyridinium chloride

3-chloro-N-methylpyridinium chloride

C

3-fluoro-N-methylpyridinium chloride

3-fluoro-N-methylpyridinium chloride

Conditions
ConditionsYield
Stage #1: N-Methylpyrrole; pyrographite With chlorotrifluoromethane at -196.15℃; Fluorination; chlorination; addition; electric arc;
Stage #2: With hydrogenchloride In methanol at -196.15℃; acidolysis;
N-Methylpyrrole
96-54-8

N-Methylpyrrole

carbon dioxide
124-38-9

carbon dioxide

pyrographite
7440-44-0

pyrographite

A

Trigonelline
535-83-1

Trigonelline

B

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
Stage #1: N-Methylpyrrole; carbon dioxide; pyrographite at -196.15℃; Addition; carboxylation; electric arc;
Stage #2: With hydrogenchloride In methanol at -196.15℃; acidolysis;
trigonelline hydrochloride
6138-41-6

trigonelline hydrochloride

A

pyridine
110-86-1

pyridine

B

nicotinic acid
59-67-6

nicotinic acid

C

1,4-dimethylpyridinium chloride
38078-47-6

1,4-dimethylpyridinium chloride

D

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
at 220℃; Product distribution; Further Variations:; Temperatures; time dependence;
N-Methylpyrrole
96-54-8

N-Methylpyrrole

<(Os(NH3)5(OTf)>(OTf)2

<(Os(NH3)5(OTf)>(OTf)2

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: -196.15 °C / electric arc
2: 0.19 mmol / HCl / methanol / -196.15 °C
View Scheme
(triphenylphosphine)gold(I) chloride
14243-64-2

(triphenylphosphine)gold(I) chloride

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

4,5-bis(cyanoethylthio)-1,3-dithiole-2-[(4,5-ethylenedithio)-1,3-dithiole-2-ylidene]
158871-27-3

4,5-bis(cyanoethylthio)-1,3-dithiole-2-[(4,5-ethylenedithio)-1,3-dithiole-2-ylidene]

[N-methylpyridinium][Au(triphenylphosphine)(2-((4,5-ethylenedithio)-1,3-dithiole-2-ylidene)-1,3-dithiole-4,5-dithionato)]
782500-50-9

[N-methylpyridinium][Au(triphenylphosphine)(2-((4,5-ethylenedithio)-1,3-dithiole-2-ylidene)-1,3-dithiole-4,5-dithionato)]

Conditions
ConditionsYield
With Na In ethanol; dichloromethane (Ar); dissolving of C8H4S8(CH2CH2CN)2 in EtOH soln. containing Na; addn.with stirring of soln. of AuCl(PEt3) and N-methylpyridinium chloride in CH2Cl2; stirring for 30 min; pptn., filtration, washing with CH2Cl2 and MeOH, drying in vac., elem. anal.;70%
1,1,2,3,3-pentacyano-propene
45078-17-9

1,1,2,3,3-pentacyano-propene

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

N-methylpyridinium 1,1,2,3,3-pentacyanopropenide
108880-12-2

N-methylpyridinium 1,1,2,3,3-pentacyanopropenide

Conditions
ConditionsYield
salt formation;
methanol
67-56-1

methanol

formic acid
64-18-6

formic acid

potassium formate
590-29-4

potassium formate

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

A

pyridine
110-86-1

pyridine

B

N-methylcyclohexylamine
626-67-5

N-methylcyclohexylamine

C

1,1-dimethyl-piperidinium chloride

1,1-dimethyl-piperidinium chloride

Conditions
ConditionsYield
at 200℃;
N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

N-methyl-3,4-didehydropiperidine
694-55-3

N-methyl-3,4-didehydropiperidine

Conditions
ConditionsYield
With sodium tetrahydroborate In ethanol at 0℃;
N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

(3R,4R)-1-Methyl-piperidine-3,4-diol

(3R,4R)-1-Methyl-piperidine-3,4-diol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: NaBH4 / ethanol / 0 °C
2: aq. H2O2; HCO2H / 168 h / 30 °C
View Scheme
copper(II) choride dihydrate

copper(II) choride dihydrate

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

1-methylpyridinium aqua-di-μ-chloro-trichlorodicuprate(II)

1-methylpyridinium aqua-di-μ-chloro-trichlorodicuprate(II)

Conditions
ConditionsYield
With H2O In hydrogenchloride mixing equimolar quantities of 1-methylpyridinium chloride and copper(II) chloride dihydrate in concd. HCl soln.;;
hydrogenchloride
7647-01-0

hydrogenchloride

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

copper dichloride

copper dichloride

A

C5H5NCH3(1+)*2Cu(2+)*5Cl(1-)*H2O=(C5H5NCH3)(Cu2Cl5(H2O))

C5H5NCH3(1+)*2Cu(2+)*5Cl(1-)*H2O=(C5H5NCH3)(Cu2Cl5(H2O))

1-methylpyridinium decachlorotetracuprate(II)

1-methylpyridinium decachlorotetracuprate(II)

Conditions
ConditionsYield
In hydrogenchloride equimolar amts. of Cu-salt and pyridinium salt in concd. HCl; crystn. on slow evapn., recrystn. in presence of excess CuCl2;
4,5-bis(benzoylthio)-1,3-dithiole-2-thione
68494-08-6

4,5-bis(benzoylthio)-1,3-dithiole-2-thione

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

copper dichloride

copper dichloride

bis(N-methyl pyridinium) bis(2-thione-1,3-dithiole-4,5-dithiolato)copper(II)

bis(N-methyl pyridinium) bis(2-thione-1,3-dithiole-4,5-dithiolato)copper(II)

Conditions
ConditionsYield
With sodium ethoxide In methanol; ethanol under N2; (PhCO)2DMIT deprotected with sodium ethoxide in EtOH; MeOH soln. of CuCl2 added with stirring; MeOH soln. of (MeNC5H5)Cl added;
N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

25,27-dihydroxy-26,28-dipropoxycalix[4]arene
143406-35-3

25,27-dihydroxy-26,28-dipropoxycalix[4]arene

C6H8N(1+)*C34H36O4*Cl(1-)

C6H8N(1+)*C34H36O4*Cl(1-)

Conditions
ConditionsYield
In chloroform-d1 at 26.84℃; Kinetics; Inert atmosphere;
N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

25,26-27,28-biscrown-3-calix<4>arene
163311-02-2

25,26-27,28-biscrown-3-calix<4>arene

C6H8N(1+)*C36H36O6*Cl(1-)

C6H8N(1+)*C36H36O6*Cl(1-)

Conditions
ConditionsYield
In chloroform-d1 at 26.84℃; Kinetics; Inert atmosphere;
N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

5-(N-phenylureido)methyl-25,26-27,28-bis(crown-3)-calix[4]arene
323208-38-4

5-(N-phenylureido)methyl-25,26-27,28-bis(crown-3)-calix[4]arene

C6H8N(1+)*C44H44N2O7*Cl(1-)

C6H8N(1+)*C44H44N2O7*Cl(1-)

Conditions
ConditionsYield
In chloroform-d1 at 26.84℃; Kinetics; Inert atmosphere;
N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

5-(N-phenylureido)methyl-26,28-dihydroxy-25,27-dipropoxycalix[4]arene

5-(N-phenylureido)methyl-26,28-dihydroxy-25,27-dipropoxycalix[4]arene

C6H8N(1+)*C42H44N2O5*Cl(1-)

C6H8N(1+)*C42H44N2O5*Cl(1-)

Conditions
ConditionsYield
In chloroform-d1 at 26.84℃; Kinetics; Inert atmosphere;
N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

N-methylcyclohexylamine
626-67-5

N-methylcyclohexylamine

Conditions
ConditionsYield
Stage #1: N-methylpyridinium chloride With hydrogen at 130℃; under 45004.5 Torr; for 12h;
Stage #2: With sodium hydroxide Temperature; Pressure;
C35H30O5

C35H30O5

N-methylpyridinium chloride
7680-73-1

N-methylpyridinium chloride

C6H8N(1+)*Cl(1-)*C35H30O5

C6H8N(1+)*Cl(1-)*C35H30O5

Conditions
ConditionsYield
In d(4)-methanol at 24.84℃; Inert atmosphere;

1-Methylpyridinium chloride Chemical Properties

IUPAC: 1-Methylpyridin-1-ium chloride 
 Methyl pyridinium chloride (7680-73-1) is also called for 1-Methylpyridinium chloride ; EINECS 231-658-9 ; N-Methylpyridinium chloride ; Pyridine methochloride ; 1-Methylpyridinium chloride ; Pyridinium, 1-methyl-, chloride ; 694-56-4(Parent) ; CID82116 and so on.
Molecular Formula: C6H8ClN
Molecular Weight: 129.59
EINECS: 231-658-9
Melting Point: 144°C
LogP: ACD/LogP: -3.59 
ACD/LogD (pH 5.5): -3.59 
ACD/LogD (pH 7.4): -3.59 
ACD/BCF (pH 5.5): 1 
ACD/BCF (pH 7.4): 1 
ACD/KOC (pH 5.5): 1 
ACD/KOC (pH 7.4): 1 
H bond acceptors: 1 
H bond donors: 0 
Freely Rotating Bonds: 0 
Topological Polar Surface Area: 3.9
Heavy Atom Count: 8
Formal Charge: 0
Complexity: 46.1
Isotope Atom Count: 0
Defined Atom StereoCenter Count: 0
Undefined Atom StereoCenter Count: 0
Defined Bond StereoCenter Count: 0
Undefined Bond StereoCenter Count: 0
Covalently-Bonded Unit Count: 2
The molecular structure of  Methyl pyridinium chloride (7680-73-1):

1-Methylpyridinium chloride Uses

 Methyl pyridinium chloride (7680-73-1) is used as chemical product.

1-Methylpyridinium chloride Toxicity Data With Reference

1.    

orl-rat LD50:285 mg/kg

    GISAAA    Gigiena i Sanitariya. 49 (1)(1984),74.
2.    

scu-rat LD50:280 mg/kg

    APFRAD    Annales Pharmaceutiques Francaises. 8 (1950),773.
3.    

orl-mus LD50:286 mg/kg

    GISAAA    Gigiena i Sanitariya. 49 (1)(1984),74.
4.    

ipr-mus LDLo:220 mg/kg

    JCINAO    Journal of Clinical Investigation. 25 (1946),908.

RTECS:  UU5950000

1-Methylpyridinium chloride Safety Profile

Poison by ingestion, subcutaneous, and intraperitoneal routes. When heated to decomposition it emits toxic fumes of Cl and NOx.

Risk Statements:  20/21/22-36/37/38
R20/21/22: Harmful by inhalation, in contact with skin and if swallowed
R36/37/38: Irritating to eyes, respiratory system and skin
Safety Statements:  36/37/39
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection

Post buying leads

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View