- Glyphosine
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- $0.00 / 1KG
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2024-09-18
- CAS:2439-99-8
- Min. Order: 1KG
- Purity: 98.0%
- Supply Ability: 1000kg/month
- Glyphosine
-
- $15.00 / 1KG
-
2021-07-13
- CAS:2439-99-8
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
- Glyphosine
-
- $15.00 / 1KG
-
2021-07-10
- CAS:2439-99-8
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| Glyphosine Basic information |
| Glyphosine Chemical Properties |
Melting point | 263°C | Boiling point | 668.4±65.0 °C(Predicted) | density | 1.952±0.06 g/cm3(Predicted) | storage temp. | +2C to +8C | solubility | PBS (pH: 7.2):5.0(Max Conc. mg/mL);19.01(Max Conc. mM) | form | Solid | pka | pK1 1.42; pK2 2.10; pK3 5.02; pK4 6.40; pK5 11.19(at 25℃) | color | White | Water Solubility | 248g/L(20 ºC) | Merck | 13,4526 | BRN | 1884944 | CAS DataBase Reference | 2439-99-8(CAS DataBase Reference) | EPA Substance Registry System | Glyphosine (2439-99-8) |
Hazard Codes | Xi | Risk Statements | 41 | Safety Statements | 26-2 | RIDADR | UN 3261 8/PG 3 | WGK Germany | 1 | RTECS | MB9120000 | HS Code | 2922.49.8000 | Toxicity | LD50 orally in rats: 3925 mg/kg; dermally in rabbits: >5010 mg/kg (Ahlrichs) |
| Glyphosine Usage And Synthesis |
Description | Glyphosine was introduced in 1973 and is preferably used in sugar beets. The synthesis starting with glycine uses two equivalents of formaldehyde and of phosphorous trichloride under oxidative conditions. A second derivative of Glyphosate is a cyclic phosphaoxazole being formed from Glyphosate and formaldehyde. This compound is claimed to control the growth of some grasses without dis- coloration or phytotoxicity.
| Uses | Application: Complexing agent; pK-values: pK1: ·2, pK2: 2.0, pK3: 5.20, pK4: 6.77, pK5: 10.89
Anti-diabetic; delay onset of diabetes in non-obese NOD mice
Glyphosine binds to a pocket of MHC class II molecules I-Ag7 and DQ8, and modify T cell responses to the autoantigenic insulin B chain fragment 9–23 (B:9–23) peptide. Glyphosine stimulate IL-10 production and delay onset of diabetes in non-obese NOD mice. | Uses | Chemical ripener; plant growth regulator. | Definition | ChEBI: A tertiary amino compound that consists of glycine bearing two N-phosphonomethyl substituents. | General Description | N,N-Bis(phosphonomethyl)glycine was present in the ligand bound to human apotransferrin. | Biochem/physiol Actions | Anti-diabetic; delay onset of diabetes in non-obese NOD mice |
| Glyphosine Preparation Products And Raw materials |
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