Glyphosate Isopropylamine Salt
| CAS Number | 38641-94-0 |
| Chemical Name | Glyphosate isopropylamine salt; N-(Phosphonomethyl)glycine isopropylamine salt;Glyphosate IPA salt;Isopropylamine salt of glyphosate |
| Molecular Weight | 228.18 g/mol |
| Molecular Formula | C₆H₁₇N₂O₅P |
| Synonyms | Glyphosate IPA salt; Isopropylamine salt of glyphosate |
| EINECS | 254-565-5 |
| Appearance | White solid or crystalline powder |
| Solubility | Soluble in water; slightly soluble in organic solvents |
| Storage conditions | Store in a sealed container, cool and dry place; protect from moisture |
Parameters of Glyphosate isopropylamine salt:
| CAS Number | 38641-94-0 |
| Chemical Name | Glyphosate isopropylamine salt; N-(Phosphonomethyl)glycine isopropylamine salt;Glyphosate IPA salt;Isopropylamine salt of glyphosate |
| Molecular Weight | 228.18 g/mol |
| Molecular Formula | C₆H₁₇N₂O₅P |
| Synonyms | Glyphosate IPA salt; Isopropylamine salt of glyphosate |
| EINECS | 254-565-5 |
| Appearance | White solid or crystalline powder |
| Solubility | Soluble in water; slightly soluble in organic solvents |
| Storage conditions | Store in a sealed container, cool and dry place; protect from moisture |
| Melting point | Decomposes above ~200°C (no distinct melting point before decomposition) |
| Boiling point | Decomposes (no boiling point under standard conditions) |
| Density | Approximately 1.3-1.4 g/cm³ (solid) |
| Vapor pressure | <0.1 mPa at 25°C (very low volatility) |
| Water solubility | ~150 g/L at 25°C (highly soluble in water) |
| LogP | Approximately -3.0 (hydrophilic, due to polar functional groups) |
Mechanism of Action
It inhibits 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) in plants, blocking the biosynthesis of aromatic amino acids (phenylalanine, tyrosine, tryptophan). This disruption of protein synthesis in plants ultimately leads to wilting and death. As a systemic herbicide, it can be absorbed through leaves and stems, then translocated to roots and meristematic tissues, exhibiting significant efficacy against perennial deep-rooted weeds.
Application Fields
Core Use: A broad-spectrum non-selective herbicide suitable for non-cultivated land (e.g., railway and highway sides), orchards, tea gardens, and farmland (e.g., fields of corn, soybeans, cotton, etc., where it must be used in conjunction with genetically modified glyphosate-resistant crops).
Target Pests: Controls annual and perennial gramineous weeds (e.g., barnyard grass, green foxtail), broad-leaved weeds (e.g., purslane, lambsquarters), and cyperaceous weeds. It also inhibits algae.
Application Method: Mostly formulated as aqueous solutions (e.g., 10% and 41% concentrations) and applied via foliar spraying. It penetrates and is absorbed through the waxy layer on plant surfaces. Weeds begin to wilt 6-7 days after application, with complete death occurring within 2-4 weeks.
Formulations and Combinations
The common formulation is soluble concentrate (SL). Due to its excellent water solubility, it can form stable formulations without requiring large amounts of adjuvants.
It is often combined with other herbicides (e.g., 2,4-D, dicamba, glufosinate) to expand the weed control spectrum and delay resistance development. A typical combined formulation is "glyphosate isopropylamine salt + 2,4-D dimethylamine salt".
Safety and Storage
Toxicity: Low toxicity, with an acute oral LD₅₀ in rats >5000 mg/kg. It has low toxicity to fish and birds but is toxic to bees (direct contact should be avoided).
Storage Conditions: Seal and store in a cool, dry, and well-ventilated place, away from fire sources, strong acids/alkalis, and food. Aqueous formulations should be protected from low-temperature freezing (which may cause demulsification).
Precautions: It is harmful to non-target plants (e.g., crop seedlings), so drift during application must be prevented. Long-term single use may lead to weed resistance, so rotation or combination with other herbicides is recommended.
Differences from Other Glyphosate Salts
Compared to ammonium salts, potassium salts, etc., glyphosate isopropylamine salt has the following core advantages:
Higher water solubility (150 g/L vs. approximately 100 g/L for the ammonium salt), allowing for higher formulation concentrations;
Slightly higher absorption efficiency by plants, resulting in faster weed control;
Better formulation stability, with less tendency to crystallize due to temperature changes. Hence, it has become the dominant glyphosate formulation globally (accounting for over 80% of the market).











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