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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

J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40241
Advantage
62
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30132
Advantage
84
Dr. J. Pharmachem (India)
Tel
+91 20 24332987
Fax
+91 20 24332137
Email
info@jpharmachem.com
Country
India
ProdList
97
Advantage
55
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696;
Email
info@hanhongsci.com
Country
China
ProdList
42982
Advantage
64
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Country
China
ProdList
32344
Advantage
50
Shandong Xiya Chemical Co., Ltd
Tel
13355009207 13355009207
Fax
0539-6365991
Email
3007715519@qq.com
Country
China
ProdList
18739
Advantage
57
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12990
Advantage
57

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  • Chelating Reagents
  • Bipyridyls, etc. (Chelating Reagents)
  • C3 to C6
  • Ketones
  • Organic Building Blocks
  • Puriss p.a.
  • General Use
  • Carbonyl Compounds
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