| Identification | Back Directory | [Name]
GLYODIN | [CAS]
556-22-9 | [Synonyms]
crag341
GLYODIN
NSC 48529
glyoxalidin
GLYOXIDE(R)
Glyoxide Dry
glyodinacetate
cragfungicide341
Glyodin(Technical)
GLYODIN, 1GM, NEAT
cragfruitfungicide341
experimentalfungicide341
Glyodin@100 μg/mL in MeOH
CRAG FRUIT FUNGICIDE 341(R)
DYMNZCGFRHLNMT-UHFFFAOYSA-N
2-heptadecylglyoxalidineacetate
2-HEPTADECYLGLYOXALDINE ACETATE
2-heptadecyl-2-imidazolinacetate
2-HEPTADECYL-2-IMIDAZOLINE ACETATE
2-heptadecyl-2-imidazolinmonoacetate
2-heptadecyl-2-imidazolinium acetate
2-IMIDAZOLINE,2-HEPTADECYL-,MONOACETATE
2-heptadecyl-4,5-dihydro-1h-imidazolmonoacetate
2-heptadecyl-4,5-dihydro-1h-imidazolylmonoacetate
4,5-Dihydro-2-heptadecyl-1H-imidazole·acetic acid
2-heptadecyl-4,5-dihydro-1H-imidazoline monoacetate | [EINECS(EC#)]
209-116-8 | [Molecular Formula]
C22H44N2O2 | [MDL Number]
MFCD00055337 | [MOL File]
556-22-9.mol | [Molecular Weight]
368.6 |
| Chemical Properties | Back Directory | [Appearance]
Light-orange crystals. Insoluble in water. | [Melting point ]
65℃ | [Boiling point ]
498.9°C (rough estimate) | [density ]
d20 1.035 | [refractive index ]
1.6300 (estimate) | [storage temp. ]
0-6°C | [Uses]
Fungicide (fruits and vegetables). | [CAS DataBase Reference]
556-22-9 | [EPA Substance Registry System]
Glyodin (556-22-9) |
| Hazard Information | Back Directory | [Chemical Properties]
Light-orange crystals. Insoluble in water. | [Definition]
ChEBI: Glyodin is an imidazole fungicide. | [Production Methods]
Detailed information on the synthesis of Glyodin is not available in open literature. However, it was probably produced through a sequence typical for long chain imidazoline fungicides, whereby industrial manufacture begins with the condensation of a long chain fatty acid (commonly stearic or heptadecanoic acid) with ethylenediamine under controlled heating to form the 2 heptadecyl 2 imidazoline ring system. This cyclodehydration step is carried out under reduced pressure to remove water and drive ring closure. The resulting imidazoline intermediate is then acetylated using acetic acid or acetic anhydride to yield the monoacetate salt, which corresponds to the commercial active ingredient glyodin. | [Mechanism of action]
Protective action. Glyodin works by disrupting enzymatic functions and essential metabolic pathways of fungi on contact | [Pesticide Type]
Algicide; Fungicide |
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