P23938

o-Phenylenediamine

flaked, 99.5%

Manufacturer: Sigma Aldrich

CAS Number: 95-54-5

Synonym(S): 1,2-Diaminobenzene, 1,2-Phenylenediamine, OPD

Select a Size

Pack Size SKU Availability Price
5 G P23938-5-G In Stock ₹ 3,453.18
100 G P23938-100-G In Stock ₹ 5,152.70
500 G P23938-500-G In Stock ₹ 7,003.78

P23938 - 5 G

₹ 3,453.18

In Stock

Quantity

1

Base Price: ₹ 3,453.18

GST (18%): ₹ 621.572

Total Price: ₹ 4,074.752

vapor density

3.7 (vs air)

Quality Level

200

vapor pressure

0.01 mmHg ( 25 °C)

Assay

99.5%

form

powder

bp

256-258 °C

mp

100-102 °C

SMILES string

Nc1ccccc1N

InChI

1S/C6H8N2/c7-5-3-1-2-4-6(5)8/h1-4H,7-8H2

InChI key

GEYOCULIXLDCMW-UHFFFAOYSA-N

Other Options

Image Product Name Manufacturer Price Range
Sigma Aldrich Fine Chemicals Biosciences o-Phenylenediamine tablet, 20 mg substrate per tablet | 95-54-5 | MFCD00007721 | 50TAB
-- ₹ 29,328.17
Sigma Aldrich Fine Chemicals Biosciences o-Phenylenediamine Peroxidase substrate, >=98.0%, powder | 95-54-5 | MFCD00007721 | 50G
-- ₹ 26,057.42
Sigma Aldrich Fine Chemicals Biosciences o-Phenylenediamine flaked, 99.5% | 95-54-5 | MFCD00007721 | 5G
-- ₹ 4,939.50
o-Phenylenediamine
-- ₹ 6,246.03
1,2-Phenylenediamine
-- ₹ 10,580.00
o-Phenylenediamine
-- ₹ 2,533.05
o-Phenylenediamine
-- ₹ 25,395.45 - ₹ 42,314.93
o-Phenylenediamine
-- ₹ 29,130.08 - ₹ 45,151.08
95-54-5 | O-Phenylenediamine
-- ₹ 1,513.00 - ₹ 15,575.00

Related Products

Img

Sigma Aldrich

695106

sublimed, ≥99%...

Img

Sigma Aldrich

P26252

97%...

Img

Sigma Aldrich

185426

≥99%...

Img

Sigma Aldrich

391085

purified by redistillation, ≥99.5%...

Img

Sigma Aldrich

185701

ReagentPlus®, 99%...

Img

Sigma Aldrich

C100005

contains 0.05% BHT as inhibitor, 97...

Img

Sigma Aldrich

398047

ACS reagent, ≥99.0%...

Img

Sigma Aldrich

407267

purified by redistillation, ≥99.5%...

Description

  • Application: o-Phenylenediamine can be used: To prepare quinoxalines, benzimidazoles, and 1H-1,5-benzodiazepines by condensing with aryl aldehydes or ketones.[1] In the H2O mediated one-pot preparation of 1,2-disubstituted benzimidazoles by reacting with aldehydes in the presence of trimethylsilyl chloride.[2]In the copper-catalyzed synthesis of alkyne substituted quinoxalines by reacting with terminal alkynes.[3]In the preparation of 1,5-benzodiazepine derivatives by reacting with different ketones under neat reaction conditions via ytterbium trichloride catalyzed condensation reaction.[4]

SAFETY INFORMATION

Pictograms

GHS06,GHS08,GHS09

Signal Word

Danger

Hazard Statements

H301,H312 + H332,H317,H319,H341,H351,H410

Precautionary Statements

P273 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - Muta. 2 - Skin Sens. 1

WGK

WGK 3

Flash Point(F)

276.8 °F - closed cup

Flash Point(C)

136 °C - closed cup