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2,2-DICHLOROPROPIONIC ACID SODIUM SALT

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2,2-DICHLOROPROPIONIC ACID SODIUM SALT Basic information

Product Name:
2,2-DICHLOROPROPIONIC ACID SODIUM SALT
Synonyms:
  • 2,2-Dichloropropionic acid sodium
  • 2-2-Dichloropionic acid sodium salt
  • 2,2-Dichloropropionic acid salt (Na)
  • dalapon-Na
  • DPA SODIUM
  • DALAPONE-NA
  • DALAPON-SODIUM
  • ALPHA,ALPHA-DICHLOROPROPIONIC ACID, SODIUM SALT
CAS:
127-20-8
MF:
C3H3Cl2NaO2
MW:
164.95
EINECS:
204-828-5
Product Categories:
  • Organics
Mol File:
127-20-8.mol
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2,2-DICHLOROPROPIONIC ACID SODIUM SALT Chemical Properties

Melting point:
166.5°C
storage temp. 
Store below +30°C.
solubility 
450g/l
form 
powder to crystal
color 
White to Orange to Green
PH
5.5 (100g/l, H2O, 20℃)
CAS DataBase Reference
127-20-8(CAS DataBase Reference)
EPA Substance Registry System
Dalapon-sodium (127-20-8)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
20/21/22-34-36/37/38
Safety Statements 
26-27-28-36/37/39-36
RIDADR 
UN 3261 8/PG 2
WGK Germany 
WGK 1 slightly water endangering
RTECS 
UF1225000
TSCA 
Yes
HS Code 
2915 90 70
HazardClass 
8
PackingGroup 
III
Toxicity
LD50 orally in Rabbit: 3860 mg/kg LD50 dermal Rabbit > 2000 mg/kg

MSDS

  • Language:English Provider:ALFA
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2,2-DICHLOROPROPIONIC ACID SODIUM SALT Usage And Synthesis

Uses

2,2-Dichloropropionic acid sodium salt is a selective, systemic herbicide used to control perennial and annual grasses on noncrop land, fruits, vegetables and some aquatic weeds.

Safety Profile

Moderately toxic by ingestion. Mutation data reported. When heated to decomposition it emits toxic fumes of Na2O and Cl-.

Environmental Fate

Soil. Undergoes dechlorination and the liberation of carbon dioxide in soil. The residual activity is limited to approximately 3–4 months (Hartley and Kidd, 1987). The average half-life for dalapon-sodium in soil incubated in the laboratory under aerobic conditions was 15 days (Namdeo, 1972)
Photolytic. Dalapon (free acid) is subject to photodegradation. When an aqueous solution (0.25 M) was irradiated with UV light at 253.7 nm at 49°C, 70% degraded in 7 hours. Pyruvic acid is formed which is subsequently decarboxylated to acetaldehy
Chemical/Physical. Slowly reacts with moisture at room temperature forming pyruvic acid (Frank and Demint, 1969; Kenaga, 1974), hydrochloric acid and sodium chloride (Kenaga, 1974; Wolfe et al., 1990). The reported hydrolysis half-life of dalapon
Products reported from the combustion of the free acid (dalapon) at 900°C include carbon monoxide, carbon dioxide, chlorine and hydrochloric acid (Kennedy et al., 1972a)

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