Chlorproguanil

1,3-Dichloro-2-propanol is a food processing contaminant . Biotransformation of 1,3-dichloro-2-propanol to epichlorohydrin by the whole cells of recombinant Escherichia coli via resin-based in situ product removal has been investigated .

1,3-Dichloro-2-propanol is a food processing contaminant . Biotransformation of 1,3-dichloro-2-propanol to epichlorohydrin by the whole cells of recombinant Escherichia coli via resin-based in situ product removal has been investigated .

Synonym(s): 2,5-Dichloronitrobenzene, Nitro-p-dichlorobenzene Formula: C6H3Cl2NO2 Formula weight: 192.00 Purity: 98% CAS Number: 89-61-2 UN Number: UN3077 Hazard Class: 9 Packing Group: III Harmonized Tariff Code:  2904.

Synonym(s): 2,5-Dichloronitrobenzene, Nitro-p-dichlorobenzene Formula: C6H3Cl2NO2 Formula weight: 192.00 Purity: 98% CAS Number: 89-61-2 UN Number: UN3077 Hazard Class: 9 Packing Group: III Harmonized Tariff Code:  2904.

1-(3-Chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one.

2,4,5-Trichlorophenol is a phenolic organochloride, which is persistent as an environmental contaminant. Application 2,4,5-Trichlorophenol may be used as an analytical reference standard for the quantification of the analyte in biological fluids

2,3-Dichloro-1-propanol belongs to the group of chloropropanols.[2] Inhibitory effects of 2,3-dichloro-1-propanol on T cell both in vivo and in vitro is reported.[2] Improved enantioselective resolution of (R,S)-2,3-dichloro-1-propanol to (S)-2,

2,3-Dichloro-1-propanol belongs to the group of chloropropanols.[2] Inhibitory effects of 2,3-dichloro-1-propanol on T cell both in vivo and in vitro is reported.[2] Improved enantioselective resolution of (R,S)-2,3-dichloro-1-propanol to (S)-2,

2,3-Dichloro-1-propanol belongs to the group of chloropropanols.[2] Inhibitory effects of 2,3-dichloro-1-propanol on T cell both in vivo and in vitro is reported.[2] Improved enantioselective resolution of (R,S)-2,3-dichloro-1-propanol to (S)-2,

2,4-Dichlorobenzoic acid was used in solid-phase extraction and gas chromatographic determination of polar acidic herbicides in surface water.2,4-Dichlorobenzoic acid was used as reagent during the synthesis of

2,4-Dichlorobenzoic acid was used in solid-phase extraction and gas chromatographic determination of polar acidic herbicides in surface water.2,4-Dichlorobenzoic acid was used as reagent during the synthesis of

2,4-Dichlorobenzoic acid was used in solid-phase extraction and gas chromatographic determination of polar acidic herbicides in surface water.2,4-Dichlorobenzoic acid was used as reagent during the synthesis of