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Formamidine hydrochloride, 98%, Thermo Scientific Chemicals
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Catalog number H60947.14
also known as H60947-14
Price (USD)/ Each
192.00
-
Quantity:
25 g
Price (USD)/ Each
192.00
Formamidine hydrochloride, 98%, Thermo Scientific Chemicals
Catalog numberH60947.14
Price (USD)/ Each
192.00
-
Chemical Identifiers
CAS6313-33-3
Specifications
Specification Sheet
Specification SheetAssay (HPLC)>97.5%
5-Methyl-4,6-dihydroxypyrimidine was synthesized from formamidine hydrochloride. N-Formimino-n-glutamate was synthesized from formamidine hydrochloride. Formamidine hydrochloride was used in the synthesis of imidazoleglycerol phosphate (IGP).
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
5-Methyl-4,6-dihydroxypyrimidine was synthesized from formamidine hydrochloride. N-Formimino-n-glutamate was synthesized from formamidine hydrochloride. Formamidine hydrochloride was used in the synthesis of imidazoleglycerol phosphate (IGP).
Solubility
Soluble in Ethanol.
Notes
Hygroscopic. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, moisture, water.
5-Methyl-4,6-dihydroxypyrimidine was synthesized from formamidine hydrochloride. N-Formimino-n-glutamate was synthesized from formamidine hydrochloride. Formamidine hydrochloride was used in the synthesis of imidazoleglycerol phosphate (IGP).
Solubility
Soluble in Ethanol.
Notes
Hygroscopic. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, moisture, water.
RUO – Research Use Only
General References:
- Shan Liu,; Qinghe Gao,; Xia Wu,; Jingjing Zhang,; Kerong Ding,; Anxin Wu. Formamidine hydrochloride as an amino surrogate: I2-catalyzed oxidative amidation of aryl methyl ketones leading to free (N-H) α-ketoamides. Org. Biomol. Chem. 2015, 13 issue , 2239-2242.
- H. M. Novais,; S. Steenken. Reactions of oxidizing radicals with 4,6-dihydroxypyrimidines as model compounds for uracil, thymine, and cytosine. J. Phys. Chem. 1977, 91 (2), 426-433.