Product Name

  • Name

    o-Phenanthroline monohydrochloride monohydrate

  • EINECS 223-325-1
  • CAS No. 3829-86-5
  • Density 1.385 g/cm3 (-100.15 C)
  • Solubility soluble in water
  • Melting Point 224-225 °C(lit.)
  • Formula C12H8N2.HCl
  • Boiling Point 365.1 °C at 760 mmHg
  • Molecular Weight 216.67
  • Flash Point 164.8 °C
  • Transport Information UN 2811 6.1/PG 3
  • Appearance white to light yellow or slightly purple powder
  • Safety 45-60-61
  • Risk Codes 25-50/53
  • Molecular Structure Molecular Structure of 3829-86-5 (o-Phenanthroline monohydrochloride monohydrate)
  • Hazard Symbols ToxicT, DangerousN
  • Synonyms 1,10-Phenanthroline,monohydrochloride (8CI,9CI);1,10-Diazaphenanthrene hydrochloride;1,10-Phenanthroline hydrochloride;NSC 4265;
  • PSA 25.78000
  • LogP 3.58500

Synthetic route

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

copper dichloride

copper dichloride

(1,5,9,13-tetraaza-3,4,7,8,11,12,15,16-tetrabenzocyclohexadeca-1,3,5,7,9,11,13,16-octaene)copper(I) nitrate

(1,5,9,13-tetraaza-3,4,7,8,11,12,15,16-tetrabenzocyclohexadeca-1,3,5,7,9,11,13,16-octaene)copper(I) nitrate

Conditions
ConditionsYield
In water from aq. soln. of CuCl2 and soln. of phenanthroline hydrochloride in 2:1, 1:1 molar ratio at pH 6.5 maintained by an alkali soln.; solvent evapd. in a water bath; ppt. washed (H2O); dried (air); elem. anal.;96%
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

copper dichloride

copper dichloride

[Cu(II)(1,10-phenantroline)2(H2O)]Cl2 complex

[Cu(II)(1,10-phenantroline)2(H2O)]Cl2 complex

Conditions
ConditionsYield
In water from aq. soln. of CuCl2 and soln. of phenanthroline hydrochloride in 1:2, 1:3 molar ratio at pH 6.5 maintained by an alkali soln.; solvent evapd. in a water bath; ppt. washed (H2O); dried (air); elem. anal.;90%
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

bis(trifluoromethane)sulfonimide lithium
90076-65-6

bis(trifluoromethane)sulfonimide lithium

C2HF6NO4S2*C12H8N2
1309962-26-2

C2HF6NO4S2*C12H8N2

Conditions
ConditionsYield
With water at 20℃; for 2h;90%
copper(II) choride dihydrate

copper(II) choride dihydrate

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

sodium p-aminobenzoate
555-06-6

sodium p-aminobenzoate

[Cu(phen)2Cl]Cl*2p‑aminobenzoic acid*4H2O

[Cu(phen)2Cl]Cl*2p‑aminobenzoic acid*4H2O

Conditions
ConditionsYield
In methanol for 1h;88%
Conditions
ConditionsYield
In methanol byproducts: Mn(2+); stirring 1:1:2:2 mixt. of copper, permanganate salt, phenanthroline deriv., NH4Cl in methanol at 50-60°C in air for 2 h; addn. of isopropanol, isolation of crystals, elem. anal.;87%
Conditions
ConditionsYield
In methanol; N,N-dimethyl-formamide byproducts: Mn(2+); stirring 1:1:2:2 mixt. of copper, permanganate salt, phenanthroline deriv., NH4Cl in methanol and DMF at 50-60°C in air for 2 h; addn. of isopropanol, isolation of crystals, elem. anal.;82%
HP(C2H5)2C6H5(1+)*Cr(NCS)4(P(C2H5)2C6H5)2(1-) = {HP(C2H5)2C6H5}{Cr(NCS)4(P(C2H5)2C6H5)2}

HP(C2H5)2C6H5(1+)*Cr(NCS)4(P(C2H5)2C6H5)2(1-) = {HP(C2H5)2C6H5}{Cr(NCS)4(P(C2H5)2C6H5)2}

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

C12H9N2(1+)*Cr(NCS)4(P(C2H5)2C6H5)2(1-) = {C12H9N2}{Cr(NCS)4(P(C2H5)2C6H5)2}

C12H9N2(1+)*Cr(NCS)4(P(C2H5)2C6H5)2(1-) = {C12H9N2}{Cr(NCS)4(P(C2H5)2C6H5)2}

Conditions
ConditionsYield
In methanol; water; butan-1-ol dissolving of amine hydrochloride in water, addn. of the phosphine-complex in methanol-butanol; filtn. after 10-15 min, washing (methanol), drying at room temp. in air, elem. anal.;72%
nitridotechnetic(VI) acid

nitridotechnetic(VI) acid

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

nitridoperoxo 1,10-phenanthroline technetium(VII)
131810-72-5

nitridoperoxo 1,10-phenanthroline technetium(VII)

Conditions
ConditionsYield
elem. anal.;70%
{HP(C2H5)2C6H4CH3}(1+)*Cr(NCS)4(P(C2H5)2C6H4CH3)2(1-) = {HP(C2H5)2C6H4CH3}{Cr(NCS)4(P(C2H5)2C6H4CH3)2}

{HP(C2H5)2C6H4CH3}(1+)*Cr(NCS)4(P(C2H5)2C6H4CH3)2(1-) = {HP(C2H5)2C6H4CH3}{Cr(NCS)4(P(C2H5)2C6H4CH3)2}

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

C12H9N2(1+)*Cr(NCS)4(P(C2H5)2C6H4CH3)2(1-) = {C12H9N2}{Cr(NCS)4(P(C2H5)2C6H4CH3)2}

C12H9N2(1+)*Cr(NCS)4(P(C2H5)2C6H4CH3)2(1-) = {C12H9N2}{Cr(NCS)4(P(C2H5)2C6H4CH3)2}

Conditions
ConditionsYield
In water dissolving of amine hydrochloride in water, addn. of Cr complex; addn. of methanol-butanol, filtn. after 10-15 min, washing (methanol), drying at room temp. in air, elem. anal.;65%
mer-diaqua(oxydiacetato)oxovanadium(IV)

mer-diaqua(oxydiacetato)oxovanadium(IV)

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

o-phenanthroline(oxydiacetato)oxovanadium(IV) monohydrate

o-phenanthroline(oxydiacetato)oxovanadium(IV) monohydrate

Conditions
ConditionsYield
In water under anaerobic conditions; water soln. of ligand (1 equiv.) added slowly to aq. soln. of V complex; left to stand for 4 d; crystals collected; elem. anal.;53%
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

A

3-bromophenanthroline
66127-01-3

3-bromophenanthroline

B

3,8-dibromo-1,10-phenathroline
100125-12-0

3,8-dibromo-1,10-phenathroline

Conditions
ConditionsYield
With bromine In nitrobenzene at 130 - 140℃; for 3h;A 33%
B 17%
With water; bromine In nitrobenzene
With bromine In bromobenzene at 135℃; for 36h;
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

3-bromophenanthroline
66127-01-3

3-bromophenanthroline

Conditions
ConditionsYield
With bromine In nitrobenzene26%
With bromine26%
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

3-anisyl-1,10-phenanthroline
879879-66-0

3-anisyl-1,10-phenanthroline

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 26 percent / Br2 / nitrobenzene
View Scheme
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

3-anisyl-2-mesityl-1,10-phenanthroline

3-anisyl-2-mesityl-1,10-phenanthroline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 26 percent / Br2 / nitrobenzene
2: 20 percent / diethyl ether
View Scheme
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

2-mesityl-8-anisyl-1,10-phenanthroline
862694-14-2

2-mesityl-8-anisyl-1,10-phenanthroline

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 26 percent / Br2 / nitrobenzene
2: 26 percent / diethyl ether
View Scheme
4-chloro-9,10-dihydro-9,10-dioxo-1-anthracenecarboxylic acid
6268-10-6

4-chloro-9,10-dihydro-9,10-dioxo-1-anthracenecarboxylic acid

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

1-chloroanthracene-9,10-dione
82-44-0

1-chloroanthracene-9,10-dione

Conditions
ConditionsYield
With 1-methyl-pyrrolidin-2-one In sulfuric acid; water
tris(acetylacetonato)vanadium(III)
13476-99-8

tris(acetylacetonato)vanadium(III)

water
7732-18-5

water

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

[(V(o-phenanthroline)2Cl)2O](2+)
767607-07-8

[(V(o-phenanthroline)2Cl)2O](2+)

Conditions
ConditionsYield
In methanol reflux in MeOH;
molybdenum (IV) sulfide

molybdenum (IV) sulfide

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

(1,10-phenanthroline)0.295MoS2

(1,10-phenanthroline)0.295MoS2

Conditions
ConditionsYield
In water prepn. from aq. dispersion of MoS2 and aq. soln. of 1,10-phenanthroline hydrochloride according to A. S. Golub et al., Solid State Ionics, 1996,vol. 91, p. 307; elem. anal.;
molybdenum (IV) sulfide

molybdenum (IV) sulfide

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

(1,10-phenanthroline)0.095MoS2

(1,10-phenanthroline)0.095MoS2

Conditions
ConditionsYield
In water prepn. from aq. dispersion of MoS2 and aq. soln. of 1,10-phenanthroline hydrochloride according to A. S. Golub et al., Solid State Ionics, 1996,vol. 91, p. 307; elem. anal.;
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

copper(II) perchlorate

copper(II) perchlorate

[Cu(phen)](2+)
15891-89-1

[Cu(phen)](2+)

Conditions
ConditionsYield
In water mixing the aq. soln. of the ligand with the metal perchlorate soln. in at least 500-fold excess; not sepd., detected in soln. by UV/VIS;
zinc(II) perchlorate

zinc(II) perchlorate

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

[Zn-1,10-phenanthroline](2+)
16561-55-0

[Zn-1,10-phenanthroline](2+)

Conditions
ConditionsYield
In water mixing the aq. soln. of the ligand with the metal perchlorate soln. in at least 500-fold excess; not sepd., detected in soln. by UV/VIS;
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

Mn(2+)*2C12H8N2*Cr2O7(2-)=Mn(C12H8N2)2Cr2O7

Mn(2+)*2C12H8N2*Cr2O7(2-)=Mn(C12H8N2)2Cr2O7

Conditions
ConditionsYield
With dichromate anion In water heating to about 80°C;
With Mn(2+) salt; Cr2O7(2-) In water heating to about 80°C;
Mo(4+)*C2O4H(1-)*3OH(1-)*H2O={Mo(C2O4H)(OH)3(H2O)}

Mo(4+)*C2O4H(1-)*3OH(1-)*H2O={Mo(C2O4H)(OH)3(H2O)}

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

C12H9N2(1+)*Mo(4+)*C2O4(2-)*2OH(1-)*Cl(1-)*H2O=C12H9N2{Mo(C2O4)(OH)2Cl(H2O)}

C12H9N2(1+)*Mo(4+)*C2O4(2-)*2OH(1-)*Cl(1-)*H2O=C12H9N2{Mo(C2O4)(OH)2Cl(H2O)}

Conditions
ConditionsYield
In water stirred; ppt. is washed (water, ethanol), dried under vac., elem. anal.;
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

nickel(II) perchlorate

nickel(II) perchlorate

[Ni(1,10-phenanthroline)](2+)
24968-26-1

[Ni(1,10-phenanthroline)](2+)

Conditions
ConditionsYield
In water mixing the aq. soln. of the ligand with the metal perchlorate soln. in at least 500-fold excess; not sepd., detected in soln. by UV/VIS;
nitrosyltrichlororhenium
15170-51-1

nitrosyltrichlororhenium

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

bis(1,10-phenanthrolinium) nitrosyldichlorotrithiocyanatorhenate

bis(1,10-phenanthrolinium) nitrosyldichlorotrithiocyanatorhenate

Conditions
ConditionsYield
With KSCN In water the Re-complex is dissolved in a soln. of KSCN; mixt. refluxed for 15 min; phenanthrolinium hydrochloride added dropwise and with stirring; ppt. changes to oily drops at water-bath temp., mother liquor is separated, oil is repeatedly washed and dried under vac., elem. anal.;
copper hydroxide
20427-59-2

copper hydroxide

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

L-proline
147-85-3

L-proline

Cu(L-prolinate)(1,10-phenanthroline)Cl*3H2O

Cu(L-prolinate)(1,10-phenanthroline)Cl*3H2O

Conditions
ConditionsYield
In ethanol; water L-proline in H2O added to freshly prepared Cu(OH)2, C12H8N2*HCl in ethanol added with gentle warming; residue removed, soln. concd. under reduced pressure, crystd., elem. anal.;
1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

copper dichloride

copper dichloride

(1,10-phenanthroline)2CuCl2

(1,10-phenanthroline)2CuCl2

Conditions
ConditionsYield
In water at pH 6; not isolated; monitored by UV;
aquo nitrosyldihydroxo oxalato rhenic acid
87331-61-1

aquo nitrosyldihydroxo oxalato rhenic acid

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

1,10-phenanthroline nitrosylchloro oxalato rhenium
87331-75-7

1,10-phenanthroline nitrosylchloro oxalato rhenium

Conditions
ConditionsYield
In water refluxing a soln. of the rhenium complex acid and 1,10-phenanthroline hydrochloride for 3 h; filtn., washing with water and ethanol, drying in vacuo, elem. anal.;
manganese(II) perchlorate

manganese(II) perchlorate

1,10-phenanthroline hydrochloride
3829-86-5

1,10-phenanthroline hydrochloride

(1,10-phenanthroline)manganese(II)
19709-60-5

(1,10-phenanthroline)manganese(II)

Conditions
ConditionsYield
In water mixing the aq. soln. of the ligand with the metal perchlorate soln. in at least 500-fold excess; not sepd., detected in soln. by UV/VIS;

1,10-Phenanthroline monohydrochloride Chemical Properties

The Molecular Structure of 1,10-Phenanthroline, hydrochloride (1:1) (CAS NO.3829-86-5):

Empirical Formula: C12H9ClN2
Molecular Weight: 216.6663 
IUPAC: 1,10-phenanthroline hydrochloride
Nominal Mass: 216 Da
Average Mass: 216.6663 Da
Monoisotopic Mass: 216.045426 Da 
Flash Point: 164.8 °C
Enthalpy of Vaporization: 58.73 kJ/mol
Boiling Point: 365.1 °C at 760 mmHg 
Melting Point: 224-225 °C(lit.)
Solubility H2O: 0.1 g/mL, clear
Water Solubility: soluble
BRN: 4007967
Appearance: white to light yellow or slightly purple powder
Vapour Pressure: 3.38E-05 mmHg at 25°C 
InChI
InChI=1/C12H8N2.ClH/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;/h1-8H;1H
Smiles
c12c3ncccc3ccc2cccn1.Cl 
Product Categories: Aromatic Hydrocarbons (substituted) & Derivatives;Heterocyclic Compounds;Analytical Chemistry;Chelating Reagents;Phenanthrolines

1,10-Phenanthroline monohydrochloride Safety Profile

Hazard Codes: ToxicTDangerousN
Risk Statements: 25-50/53 
R25 :Toxic if swallowed
R50/53:Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment
Safety Statements: 45-60-61 
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
S60:This material and its container must be disposed of as hazardous waste
S61:Avoid release to the environment. Refer to special instructions / safety data sheets
RIDADR UN: 2811 6.1/PG 3
WGK Germany: 3
F 8:Photosensitive
HazardClass: 6.1
PackingGroup :III

1,10-Phenanthroline monohydrochloride Specification

 1,10-Phenanthroline, hydrochloride (1:1)  (CAS NO.3829-86-5) is also called as 1,10-Diazaphenanthrene hydrochloride ; 1,10-Phenanthroline hydrochloride ; EINECS 223-325-1 ; NSC 4265 ; Phenanthroline hydrochloride ; 1,10-Phenanthroline monohydrochloride monohydrate ; 1,10-Phenanthroline, monohydrochloride .

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