2,2-DICHLOROPROPIONIC ACID SODIUM SALT
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
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)
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
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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2,2-DICHLOROPROPIONIC ACID SODIUM SALT(127-20-8)Related Product Information
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