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615-28-1 Usage

Uses

Different sources of media describe the Uses of 615-28-1 differently. You can refer to the following data:
1. o-Phenylenediamine is a peroxidase substrate suitable for use in ELISA procedures. The substrate produces a soluble end product that is orange-brown in color and can be read spectrophotometrically at 450 nm. The OPD reaction may be stopped with 3 N HCl or 3 M H2SO4 and read at 492 nm.
2. o-Phenylenediamine dihydrochloride has been used as a substrate for horseradish-peroxidase-conjugated secondary antibody in enzyme-linked immunosorbent assay (ELISA).

General Description

Brownish-yellow crystals. Slightly soluble in water. Used in the manufacture of dye.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

Acidic organic/inorganic salts, such as OPD EASY-tablets, are generally soluble in water. The resulting solutions contain moderate to high concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.

Purification Methods

Crystallise the salt from dilute HCl (60mL conc HCl, 40mL water, with 2g stannous chloride), after treatment of the hot solution with charcoal by adding an equal volume of conc HCl and cooling in an ice-salt mixture. The crystals are washed with a small amount of conc HCl and dried in a vacuum desiccator over NaOH. [Beilstein 13 IV 38.]

Check Digit Verification of cas no

The CAS Registry Mumber 615-28-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 615-28:
(5*6)+(4*1)+(3*5)+(2*2)+(1*8)=61
61 % 10 = 1
So 615-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2.2ClH/c7-5-3-1-2-4-6(5)8;;/h1-4H,7-8H2;2*1H

615-28-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • TCI America

  • (P1144)  1,2-Phenylenediamine Dihydrochloride [for Biochemical Research]  >98.0%(HPLC)(N)

  • 615-28-1

  • 1g

  • 220.00CNY

  • Detail
  • TCI America

  • (P1144)  1,2-Phenylenediamine Dihydrochloride [for Biochemical Research]  >98.0%(HPLC)(N)

  • 615-28-1

  • 5g

  • 480.00CNY

  • Detail
  • Aldrich

  • (78440)  o-Phenylenediaminedihydrochloride  ≥99.0% (AT)

  • 615-28-1

  • 78440-50G

  • 3,049.02CNY

  • Detail

615-28-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name OPD EASY-tablets

1.2 Other means of identification

Product number -
Other names benzene-1,2-diamine,dihydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:615-28-1 SDS

615-28-1Synthetic route

1,1,1-trifluoroacetophenone
434-45-7

1,1,1-trifluoroacetophenone

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-phenyl-1H-benzoimidazole
716-79-0

2-phenyl-1H-benzoimidazole

Conditions
ConditionsYield
In N,N-dimethyl acetamide at 120 - 130℃; for 24h;99.6%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

ethyl acetate
141-78-6

ethyl acetate

2-Methyl-1H-benzimidazole
615-15-6

2-Methyl-1H-benzimidazole

Conditions
ConditionsYield
In ethylene glycol for 0.025h; microwave irradiation;99%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

Ethyl propionate
105-37-3

Ethyl propionate

2-ethylbenzimidazole
1848-84-6

2-ethylbenzimidazole

Conditions
ConditionsYield
In ethylene glycol for 0.025h; microwave irradiation;99%
ethyl 2-hydroxyacetate
623-50-7

ethyl 2-hydroxyacetate

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-(Hydroxymethyl)benzimidazole
4856-97-7

2-(Hydroxymethyl)benzimidazole

Conditions
ConditionsYield
In ethylene glycol for 0.025h; microwave irradiation;97%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

benzil
134-81-6

benzil

2,3-diphenylquinoxaline
1684-14-6

2,3-diphenylquinoxaline

Conditions
ConditionsYield
In water at 230℃; for 0.166667h; Microwave irradiation; Green chemistry;97%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

chloroacetic acid ethyl ester
105-39-5

chloroacetic acid ethyl ester

2-chloromethyl-1H-benzimidazole
4857-04-9

2-chloromethyl-1H-benzimidazole

Conditions
ConditionsYield
In ethylene glycol for 0.025h; microwave irradiation;95%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

4-amino-benzoic acid
150-13-0

4-amino-benzoic acid

4-(1H-benzimidazol-2-yl)aniline
2963-77-1

4-(1H-benzimidazol-2-yl)aniline

Conditions
ConditionsYield
With PPA for 0.0833333h; microwave irradiation;94.8%
Ethyl hexanoate
123-66-0

Ethyl hexanoate

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-pentyl-1H-benzoimidazole
5851-46-7

2-pentyl-1H-benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 0.025h; microwave irradiation;94%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

formic acid ethyl ester
109-94-4

formic acid ethyl ester

benzoimidazole
51-17-2

benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 0.025h; microwave irradiation;94%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

diethyl malonate
105-53-3

diethyl malonate

bis(1H-benzo[d]imidazol-2-yl)methane
5999-14-4

bis(1H-benzo[d]imidazol-2-yl)methane

Conditions
ConditionsYield
In ethylene glycol for 0.025h; microwave irradiation;92%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

acetic acid
64-19-7

acetic acid

2-Methyl-1H-benzimidazole
615-15-6

2-Methyl-1H-benzimidazole

Conditions
ConditionsYield
In water for 0.0222222h; microwave irradiation;89.01%
With hydrogenchloride In water for 4h; Inert atmosphere; Reflux;68%
Stage #1: o-phenylenediamine dihydrochloride; acetic acid In water for 0.75h; Reflux;
Stage #2: With ammonia In water
60%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

para-chlorobenzoic acid
74-11-3

para-chlorobenzoic acid

2-(4-chlorophenyl)benzimidazole
1019-85-8

2-(4-chlorophenyl)benzimidazole

Conditions
ConditionsYield
With PPA for 0.075h; microwave irradiation;88.63%
trans-2-chlorocinnamic acid
704-96-1

trans-2-chlorocinnamic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

(E)-2-(2-chlorostyryl)-1H-benzo[d]imidazole
151330-84-6

(E)-2-(2-chlorostyryl)-1H-benzo[d]imidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;88%
(E)-2-methyl-3-(4-nitrophenyl)acrylic acid
13048-77-6, 949-98-4, 13048-76-5

(E)-2-methyl-3-(4-nitrophenyl)acrylic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-[1-methyl-2-(4-nitro-phenyl)-vinyl]-1H-benzoimidazole
336181-48-7

2-[1-methyl-2-(4-nitro-phenyl)-vinyl]-1H-benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;88%
3,3-diphenylacrylic acid
606-84-8

3,3-diphenylacrylic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-(2,2-diphenyl-vinyl)-1H-benzoimidazole

2-(2,2-diphenyl-vinyl)-1H-benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;86%
4-nitro-trans-cinnamic acid
882-06-4

4-nitro-trans-cinnamic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

(E)-2-(4-nitrostyryl)-1H-benzo[d]imidazole
28940-47-8

(E)-2-(4-nitrostyryl)-1H-benzo[d]imidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;86%
(E)-3-phenylacrylic acid
140-10-3

(E)-3-phenylacrylic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

(E)-2-styryl-1H-benzo[d]imidazole
58758-09-1

(E)-2-styryl-1H-benzo[d]imidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;85%
bromocyane
506-68-3

bromocyane

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

1H-benzimidazol-2-amine
934-32-7

1H-benzimidazol-2-amine

Conditions
ConditionsYield
Stage #1: bromocyane; o-phenylenediamine dihydrochloride With sodium hydrogencarbonate In water; acetonitrile at 0 - 20℃;
Stage #2: With sodium carbonate In water; acetonitrile
85%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

benzoic acid
65-85-0

benzoic acid

2-phenyl-1H-benzoimidazole
716-79-0

2-phenyl-1H-benzoimidazole

Conditions
ConditionsYield
With PPA for 0.075h; microwave irradiation;84.83%
(E)-3-Nitrocinnamic acid
555-68-0

(E)-3-Nitrocinnamic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-(3-nitro-styryl)-1H-benzoimidazole
55969-91-0

2-(3-nitro-styryl)-1H-benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;84%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

acetone
67-64-1

acetone

2,2,4-trimethyl-2,3-dihydro-1H-1,5-benzodiazepine
24107-34-4

2,2,4-trimethyl-2,3-dihydro-1H-1,5-benzodiazepine

Conditions
ConditionsYield
In water at 20℃; for 7h;83%
With sodium hydroxide for 18h; Ambient temperature; gas/solid reaction;
-2-methyl-3-(4-chlorophenyl)prop-2-enoic acid
1202-60-4, 66482-40-4, 14328-88-2

-2-methyl-3-(4-chlorophenyl)prop-2-enoic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-[2-(4-chloro-phenyl)-1-methyl-vinyl]-1H-benzoimidazole
336181-46-5

2-[2-(4-chloro-phenyl)-1-methyl-vinyl]-1H-benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;83%
3-(4-chlorophenyl)prop-2-enoic acid
1615-02-7

3-(4-chlorophenyl)prop-2-enoic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

(E)-2-(4-chlorostyryl)-1H-benzo[d]imidazole
206982-69-6

(E)-2-(4-chlorostyryl)-1H-benzo[d]imidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;82%
-2-methyl-3-(4-methylphenyl)prop-2-enoic acid
25860-59-7, 66482-35-7, 32655-80-4

-2-methyl-3-(4-methylphenyl)prop-2-enoic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-(1-methyl-2-p-tolyl-vinyl)-1H-benzoimidazole
336181-44-3

2-(1-methyl-2-p-tolyl-vinyl)-1H-benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;82%
o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

chloroacetic acid
79-11-8

chloroacetic acid

2-chloromethyl-1H-benzimidazole
4857-04-9

2-chloromethyl-1H-benzimidazole

Conditions
ConditionsYield
In water for 1.5h; Reflux;82%
4-butanolide
96-48-0

4-butanolide

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

3-(1H-Benzoimidazol-2-yl)-propan-1-ol; hydrochloride

3-(1H-Benzoimidazol-2-yl)-propan-1-ol; hydrochloride

Conditions
ConditionsYield
With boric acid In toluene for 12h; Reflux;81%
(E)-3-phenyl-2-butenoic acid
704-80-3

(E)-3-phenyl-2-butenoic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-(2-phenyl-propenyl)-1H-benzoimidazole

2-(2-phenyl-propenyl)-1H-benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;80%
2-methyl-3-(3-nitrophenyl)propenoic acid
124525-54-8

2-methyl-3-(3-nitrophenyl)propenoic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

2-[1-methyl-2-(3-nitro-phenyl)-vinyl]-1H-benzoimidazole
336181-47-6

2-[1-methyl-2-(3-nitro-phenyl)-vinyl]-1H-benzoimidazole

Conditions
ConditionsYield
In ethylene glycol for 5h; Condensation; Cycloaddition; Heating;80%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

(C6H10N2)(MoOCl5)

(C6H10N2)(MoOCl5)

Conditions
ConditionsYield
With HCl In water N2 atmosphere; diamine dihydrochloride added to the soln. of MoCl5 in 12 M HCl (shaking) and dry HCl passed into the soln. for 1-2 h; redn. of the soln. volume to one third by gently heating; passing dry HCl into the soln. (ice-cooling); pptd. crystals vacuum-filtered, washed with ether/thionyl chloride (1:1) to avoid hydrolysis and dried over KOH; elem. anal.;80%
(E/Z)-16-hydroxyhexadec-9-enoic acid
17278-80-7

(E/Z)-16-hydroxyhexadec-9-enoic acid

o-phenylenediamine dihydrochloride
615-28-1

o-phenylenediamine dihydrochloride

C22H34N2O

C22H34N2O

Conditions
ConditionsYield
In ethylene glycol at 150 - 200℃;79%

615-28-1Relevant articles and documents

Reduction of dinitrobenzenes by electron-carrying catalysts in the electrosynthesis of diaminobenzenes

Abakumov, M. V.,Leonova, M. Yu.,Mikhalchenko, L. V.,Novikov, V. T.,Zaplavin, A. P.

, p. 1927 - 1933 (2021/11/05)

The interaction of isomeric dinitrobenzenes (DNBs) with titanium(III), tin(II), and vanadium(II) chlorides, which are reducing agents used as electron carriers in the electrosynthesis of diaminobenzenes, has been studied. Rate constants of the reduction of isomeric DNBs and nitrophenylhydroxylamines by SnCl2 and TiCl3 in a 2 M water-alcohol solution (10 vol.% C2H5OH) of HCl were measured, and activation energies of the reduction of isomeric DNBs were determined. The rates of interaction of DNBs with the listed mediators increase in the series SnCl2 3 2. It is shown that the electrolysis of DNBs in the presence of an excess of these mediators makes it possible to obtain the corresponding diaminobenzenes with a yield of 60–90%.

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