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Chloranilic acid

Product Name
Chloranilic acid
CAS No.
87-88-7
Chemical Name
Chloranilic acid
Synonyms
NSC 6108;NSC 97383;chloranilic;CHLORANILIC ACID;p-chloranilicacid;TIMTEC-BB SBB008913;CHLORANILIC ACID AR;Chloranilic Acid >Chloranilic acid, GR;Chloranilic acid, 99+%
CBNumber
CB9376018
Molecular Formula
C6H2Cl2O4
Formula Weight
208.98
MOL File
87-88-7.mol
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Chloranilic acid Property

Melting point:
≥300 °C (lit.)
Boiling point:
300.11°C (rough estimate)
Density 
1.93
refractive index 
1.4570 (estimate)
storage temp. 
Amber Vial, Refrigerator
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
pK1:1.09;pK2:2.42 (25°C)
form 
Fine Powder
color 
Orange to red
Odor
Odorless
Water Solubility 
Soluble in hot water and methanol. Insoluble in organic solvents.
Merck 
14,2079
BRN 
1875040
Stability:
Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference
87-88-7(CAS DataBase Reference)
EPA Substance Registry System
2,5-Cyclohexadiene-1,4-dione, 2,5-dichloro-3,6-dihydroxy- (87-88-7)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
DK4005000
TSCA 
Yes
HS Code 
29147000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
C8136
Product name
Chloranilic acid
Purity
≥98%
Packaging
25g
Price
$71.4
Updated
2024/03/01
TCI Chemical
Product number
C0077
Product name
Chloranilic Acid
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$79
Updated
2024/03/01
Alfa Aesar
Product number
A10493
Product name
Chloranilic acid, 98+%
Packaging
25g
Price
$40.8
Updated
2024/03/01
Alfa Aesar
Product number
A10493
Product name
Chloranilic acid, 98+%
Packaging
100g
Price
$106.65
Updated
2024/03/01
Alfa Aesar
Product number
A10493
Product name
Chloranilic acid, 98+%
Packaging
500g
Price
$565
Updated
2024/03/01
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Chloranilic acid Chemical Properties,Usage,Production

Chemical Properties

orange or red crystals or powder

Uses

Chloranilic acid is the reactant involved in:
Acting as a proton donor in reactions studying dimensionality control
Synthesis of dimethylbipyridyl complexes
Synthesis of (nonylbenzimidazolylmethyl)benzene for preparation of neutral altitudinal rotor-shaped dirhenium metallacycles
Charge-transfer reactions with metoprolol tartrate
Salt formation with organic bases
Synthesis of osmium metalla-rectangles with anticancer activity

Uses

Chloranilic acid is a strong dibasic organic acid which exhibits electron-acceptor properties on one hand and acidic properties leading to formation of hydrogen bonds on the other hand.
Chloranilic acid is used in spectrophotometry. It reacts with metal ions to form stable complexes. It is also used as a reactant in the preparation of dimethylbipyridyl complexes and (nonylbenzimidazolylmethyl)benzene. Further, it is used in charge-transfer reactions with metoprolol tartrate. It is also employed in the synthesis of osmium metalla-rectangles with anticancer activity. In addition to this, it has potential antibacterial activities against methicillin-resistant Staphylococcus aureus.

Uses

Reacts with metal cations to form stable salts. Used in spectrophotometry: Hart, organic. Chem. Bull. 33, no. 3 (1961).

Purification Methods

A solution of 8g of quinone in 1L of boiling water is filtered while hot, then extracted twice at about 50o with 200mL portions of *benzene. The aqueous phase is cooled in ice-water. The crystals are filtered off, washed with three 10mL portions of water, and dried at 115o. It can be sublimed in vacuo. [Weissbart & Rysselberghe J Phys Chem 61 765 1957.] The diacetate has m 182-185o [Conant & Fieser J Am Chem Soc 46 1866 1924, Thamer & Voight J Phys Chem 56 225 1952]. [Beilstein 8 IV 2707.]

Chloranilic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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Chloranilic acid Suppliers

Carbosynth
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
Advantage
58
Molekula Limited
Tel
--
Fax
--
Email
o@molekula.com
Country
United Kingdom
ProdList
6127
Advantage
58
CMS Chemicals Limited
Tel
--
Fax
--
Email
cms.marketing@cms-chemicals.com
Country
United Kingdom
ProdList
3708
Advantage
60
Glentham Life Sciences
Tel
--
Fax
--
Email
info@glenthamls.com
Country
United Kingdom
ProdList
1429
Advantage
0
Leancare Ltd.
Tel
--
Fax
--
Email
enquiry@leancare.co.uk
Country
United Kingdom
ProdList
6446
Advantage
42
ARIAC - Armenian Institute of Applied Chemistry
Tel
--
Fax
--
Email
ariac@web.am
Country
United Kingdom
ProdList
2466
Advantage
46
MOLEKULA Ltd.
Tel
--
Fax
--
Email
kevinbanks@molekula.com
Country
United Kingdom
ProdList
6140
Advantage
66
Eurolabs Limited
Tel
--
Fax
--
Country
United Kingdom
ProdList
6309
Advantage
46
Lansdowne Chemicals Plc
Tel
--
Fax
--
Email
robert.moss@lansdownechemicals.com
Country
United Kingdom
ProdList
576
Advantage
51
VWR International
Tel
--
Fax
--
Email
solutions@vwr.com
Country
United Kingdom
ProdList
6548
Advantage
82

87-88-7, Chloranilic acidRelated Search:


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  • 2,5-Dichloro-3,6-dihydroxy-p-benzoquinone 2,5-Dichloro-3,6-dihydroxy-1,4-benzoquinone 2,5-Dichloro-3,6-dihydroxy-p-quinone
  • NSC 6108
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  • TIMTEC-BB SBB008913
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  • 2,5-Cyclohexadiene-1,4-dione,2,5-dichloro-3,6-dihydroxy-
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  • 87-88-7
  • C6Cl2O2OH2
  • C6H2Cl2O4
  • C6H2O4Cl2
  • Benzoquinones
  • Chelating Reagents
  • Bipyridyls, etc. (Chelating Reagents)
  • C3 to C6
  • Ketones
  • Organic Building Blocks
  • Puriss p.a.
  • General Use
  • Carbonyl Compounds
  • Building Blocks
  • Analytical Reagents
  • Analytical Chromatography Product Catalog
  • Inhibitors