ChemicalBook > CAS DataBase List > 2,3-Dichloro-1,4-naphthoquinone

2,3-Dichloro-1,4-naphthoquinone

Product Name
2,3-Dichloro-1,4-naphthoquinone
CAS No.
117-80-6
Chemical Name
2,3-Dichloro-1,4-naphthoquinone
Synonyms
CNQ;usr604;Phygon;USR 604;ent3776;Quintar;DICHLON;Diclone;Uniroyal;ent3,776
CBNumber
CB3469109
Molecular Formula
C10H4Cl2O2
Formula Weight
227.04
MOL File
117-80-6.mol
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2,3-Dichloro-1,4-naphthoquinone Property

Melting point:
194-197 °C (lit.)
Boiling point:
275 °C (2 mmHg)
Density 
1.4057 (rough estimate)
vapor pressure 
0Pa at 20℃
refractive index 
1.5410 (estimate)
Flash point:
275°C/2mm
storage temp. 
Store below +30°C.
form 
Fine Crystalline Powder
color 
Yellow
Water Solubility 
0.008 g/L
Merck 
14,3045
BRN 
1073511
LogP
2.9 at 23℃
CAS DataBase Reference
117-80-6(CAS DataBase Reference)
NIST Chemistry Reference
1,4-Naphthalenedione, 2,3-dichloro-(117-80-6)
EPA Substance Registry System
Dichlone (117-80-6)
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Safety

Hazard Codes 
Xn,N
Risk Statements 
22-36/38-50/53
Safety Statements 
26-60-61
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
RTECS 
QL7525000
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29147090
Hazardous Substances Data
117-80-6(Hazardous Substances Data)
Toxicity
LD50 orally in rats: 1300 mg/kg (Bailey, White)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H301Toxic if swalloed

H315Causes skin irritation

H319Causes serious eye irritation

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P273Avoid release to the environment.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

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
45434
Product name
Dichlon
Purity
PESTANAL
Packaging
1ea
Price
$28.2
Updated
2024/03/01
Sigma-Aldrich
Product number
35990
Product name
2,3-Dichloro-1,4-naphthoquinone
Purity
for spectrophotometric det. of hydrazides, ≥98.0%
Packaging
100g
Price
$36.7
Updated
2022/05/15
TCI Chemical
Product number
D0384
Product name
2,3-Dichloro-1,4-naphthoquinone
Purity
>95.0%(GC)(T)
Packaging
25g
Price
$18
Updated
2024/03/01
TCI Chemical
Product number
D0384
Product name
2,3-Dichloro-1,4-naphthoquinone
Purity
>95.0%(GC)(T)
Packaging
500g
Price
$106
Updated
2024/03/01
Alfa Aesar
Product number
A13378
Product name
2,3-Dichloro-1,4-naphthoquinone, 98%
Packaging
25g
Price
$21.65
Updated
2024/03/01
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2,3-Dichloro-1,4-naphthoquinone Chemical Properties,Usage,Production

Chemical Properties

YELLOW FINE CRYSTALLINE POWDER

Uses

Fungicide used on fruits, field crops and vegetables

Uses

Use in textiles, as organic catalyst, as chemical intermediate, as additive in dye binders. Also used as an important catalyst to produce 3,3-dichlorobenzene.

Uses

Fungicide for agriculture and textiles; herbicide.

General Description

2,3-Dichloro-1,4-naphthoquinone is a yellow crystalline solid dissolved in a water-emulsifiable liquid carrier. Can cause illness by inhalation, skin absorption and/or ingestion. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Can easily penetrate the soil and contaminate groundwater and nearby streams. Used as a fungicide.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

2,3-Dichloro-1,4-naphthoquinone is a halogenated ketone. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.

Health Hazard

INHALATION: Irritation to mucous membrane. EYES: Irritation. SKIN: Irritation. INGESTION: Can cause CNS depression.

Fire Hazard

Special Hazards of Combustion Products: Highly toxic fumes are imminent.

Flammability and Explosibility

Not classified

Agricultural Uses

Fungicide: Not currently registered in the U.S. Not approved for use in the EU. Dichlone is used as a fungicide for foliage and to control blue algae in ponds, swimming pools and lakes. As a substitute for copper and sulfur to control rot on fruit trees, vegetables, field crops, ornamentals, resident and commercial outdoor areas.

Trade name

ALGISTAT®; COMPOUND 604®; PHYGON®; PHYGON® PASTE; PHYGON® SEED PROTECTANT; PHYGON® XL; QUINTAR®; QUINTAR® 540F; SANQUINON®; UNIROYAL® 604; USR® 604; U.S. RUBBER® 604

Safety Profile

Poison by ingestion and intraperitoneal routes. Mildly toxic by skin contact. A skin, eye, and mucous membrane irritant. Large doses can cause central nervous system depression. Questionable carcinogen with experimental carcinogenic and neoplastigenic data. A fungcide and algicide. When heated to decomposition it emits toxic fumes of Cl-. See also CHLORIDES.

Environmental Fate

Plant. In plants, dichlone loses both chlorine atoms and are replaced by sulphydryl groups to give a substituted dimercapto compound (Hartley and Kidd, 1987).
Photolytic. The UV absorption band for dichlone is 330 nm (Gore et al., 1971). Irradiation of dichlone in a variety of organic solvents (benzene, isopropanol, ethanol) using UV light produced a number of dehalogenated compounds. In the absence or presence of oxygen, 2-chloro-1,4-naphthoquinone, 1,4-naphthoquinone and 1,4-naphthalenediol were produced. Further irradiation in the presence of oxygen yielded phthalic acid and phthalic anhydride as the major products. In a mixture of benzene and isopropanol, dichlone degraded to the minor products: 2-chloro-3-hydroxy-1,4-naphthoquinone, 2- chloro-3-phenoxy-1,4-naphthoquinone, 2,3-dichloro-4-hydroxy-1-keto-2-phenyl-1,2- dihydronaphthalene and isopropyl-1-chloro-2,3-dioxo-1-indanecarboxylate (Ide et al., 1979).
Chemical/Physical. Emits toxic fumes of chlorine when heated to decomposition (Sax and Lewis, 1987).

Purification Methods

Crystallise the quinone from EtOH. [Beilstein 7 IV 2426.]

2,3-Dichloro-1,4-naphthoquinone Preparation Products And Raw materials

Raw materials

FUMING SULFURIC ACID dilute sulphuric acid Ferric chloride Naphthionic acid 1,4-Naphthoquinone Government regulation Iron 1,3-Dinitrobenzene

Preparation Products

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View Lastest Price from 2,3-Dichloro-1,4-naphthoquinone manufacturers

Hebei Chuanghai Biotechnology Co,.LTD
Product
2,3-Dichloro-1,4-naphthoquinone 117-80-6
Price
US $5.00-2.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10000kg
Release date
2024-08-22
Zhuozhou Wenxi import and Export Co., Ltd
Product
2,3-Dichloro-1,4-naphthoquinone 117-80-6
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-06-27
Career Henan Chemical Co
Product
2,3-Dichloro-1,4-naphthoquinone 117-80-6
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
100KG
Release date
2019-05-24

117-80-6, 2,3-Dichloro-1,4-naphthoquinoneRelated Search:

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