4-Methoxy-o-phenylenediamine, 98%, Thermo Scientific Chemicals
4-Methoxy-o-phenylenediamine, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-Methoxy-o-phenylenediamine, 98%, Thermo Scientific Chemicals

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25 g
1 g
5 g
產品號碼 A15557.14
亦稱為 A15557-14
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25 g
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化學識別
CAS102-51-2
IUPAC Name4-methoxybenzene-1,2-diamine
Molecular FormulaC7H10N2O
InChI KeyAGAHETWGCFCMDK-UHFFFAOYSA-N
SMILESCOC1=CC=C(N)C(N)=C1
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規格Specification Sheet規格表
Appearance (Color)Grey or brown or purple
Assay (GC)>97.5%
Formcrystalline or fused solid
4-Methoxy-o-phenylenediamine is widely used as an intermediate in organic synthesis and pharmaceuticals. It is an important precursor for the synthesis of other heterocyclic compounds. It is used in the determination of glyoxal, methylglyoxal, and diacetyl in urine using 4-methoxy-o-phenylenediamine as a derivatizing reagent by High-performance liquid chromatography (HPLC).

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-Methoxy-o-phenylenediamine is widely used as an intermediate in organic synthesis and pharmaceuticals. It is an important precursor for the synthesis of other heterocyclic compounds. It is used in the determination of glyoxal, methylglyoxal, and diacetyl in urine using 4-methoxy-o-phenylenediamine as a derivatizing reagent by High-performance liquid chromatography (HPLC).

Solubility
Soluble in dimethyl sulfoxide and methanol.

Notes
Air sensitive and Hygroscopic. Incompatible with acids, acid chlorides, acid anhydrides, chloroformates and strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Ojeda, A. G.; Wrobel, K.; Escobosa, A. R. C.; Sevilla, E. G.; Wrobel, K. High-performance liquid chromatography determination of glyoxal, methylglyoxal, and diacetyl in urine using 4-methoxy-o-phenylenediamine as derivatizing reagent. Anal. Biochem. 2014, 449, 52-58.
  2. Vadagaonkar, K. S.; Kalmode, H. P.; Mrugan, K.; Chaskar, A. C. I2 catalyzed tandem protocol for synthesis of quinoxalines via sp3, sp2and sp C-H functionalization. RSC Adv. 2015, 5 (8), 5580-5590.