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| | Hydroxylamine hydrochloride Basic information |
| | Hydroxylamine hydrochloride Chemical Properties |
| Melting point | 155-157 °C (dec.)(lit.) | | density | 1.67 g/mL at 25 °C(lit.) | | vapor pressure | 0.054 Pa (50 °C) | | storage temp. | Store at +15°C to +25°C. | | solubility | 470g/l | | form | Liquid | | color | White to off-white | | PH | 2.5-3.5 (25℃, 50mg/mL in H2O) | | Water Solubility | 560 g/L (20 ºC) | | Sensitive | Hygroscopic | | Merck | 14,4828 | | BRN | 3539763 | | Stability: | Substances to be avoided include strong oxidizing agents. Heating above 115 C may cause explosion; do not store above 65C. Moisture and air sensitive. | | InChIKey | WTDHULULXKLSOZ-UHFFFAOYSA-N | | LogP | -0.810 (est) | | CAS DataBase Reference | 5470-11-1(CAS DataBase Reference) | | EPA Substance Registry System | Hydroxylamine hydrochloride (5470-11-1) |
| | Hydroxylamine hydrochloride Usage And Synthesis |
| Description | Hydroxylamine hydrochloride is a reducing agent that is routinely used for the deacetylation of SATA to form free sulfhydryls (Figure 1), for cleavage of protein cross‐linkers that contain carbonyl groups (i.e. EGS) and for mutagenesis of plasmid DNA.
Hydroxylamine converts aldehydes and ketones (carbonyls) to their oxime derivative in weak bases, therefore cross‐linkers and other compounds with carbonyl groups are cleavable with Hydroxylamine hydrochloride.
SATA and SATP are modification reagents that add a sulfhydryl group to primary amines on biomolecules. The initial modification results in the addition of an acetyl‐protected sulfur enabling storage of the biomolecule. To generate a free sulfhydryl the biomolecule is treated with hydroxylamine to remove the protecting acetyl group (see figure).
EGS and sulfo‐EGS are homobifunctional, succinimidyl ester, amine reactive crosslinkers that are resistant to cleavage by denaturants used in SDS‐PAGE conditions, but may be cleaved with hydroxylamine. | | Chemical Properties | Hydroxylamine Hydrochloride(NH2OH.HCl) is an inorganic compound that is the hydrochloric acid salt of hydroxylamine. It is highly hygroscopic and decomposes when exposed to dampness above 151℃. This compound is primarily used as a reducing agent and imaging agent and is instrumental in the preparation of oximes in organic synthesis. It can convert aldehydes and ketones to oximes and acid chlorides to hydroxamic acids. However, This product is highly toxic and irritating to the skin. | | Physical properties | It is a colorless monoclinic crystal that is hygroscopic and decomposes slowly in moist air. It has a density of 1.67 g/cm3 at a temperature of 17°C and melts at 151°C with decomposition. It is highly soluble in water, with a solubility of 84g/100g at 20°C, and is also soluble in lower alcohols and glycols. A 0.1 molar solution of this substance has a pH of 3.4. | | Uses | Hydroxylamine hydrochloride is a monomoamine oxidase inhibitor. It is used to prepare oximes and hydroxmic acids in organic synthesis. It acts as a copolymerization inhibitor. It can be used to remove bromine and polybromide from a solution during extraction of lignin from lignocellulosic biomass. It is key starting material for the preparation of pharmaceuticals and agrochemicals. It plays a vital role in rubber and plastic industries as an antioxidant, a vulcanization accelerator and a radical scavenger. It is also used as a color stabilizer and emulsion additive in color films. | | Definition | ChEBI: Hydroxylamine hydrochloride is an organic molecular entity. It is a colorless inorganic compound (HONH2) used in organic synthesis and as a reducing agent, due to its ability to donate nitric oxide. | | Preparation | Hydroxylamine hydrochloride is prepared by electrolytic reduction of ammonium chloride. Or by the action of nitromethane with hydrochloric acid and water to obtain hydroxylamine hydrochloride. | | Biotechnological Applications | Hydroxylamine hydrochloride is a strong reducing agent that is useful in biochemical crosslinking applications, including the deacetylation of SATA and chemical cleavage of EGS and Sulfo-EGS. Hydroxylamine converts carbonyl compounds (aldehydes and ketones) to their oxime derivatives in the presence of a weak base. Therefore, crosslinkers and other compounds that contain a carbonyl within their structure are cleavable with hydroxylamine?HCl.
MAN0011201_HydroxylamineHCl_UG.pdf | | General Description | Hydroxylamine hydrochloride appears as colorless or off-white crystalline solid. pH (0.1 molar aqueous solution) 3.4. pH (0.2 molar aqueous solution) 3.2. (NTP, 1992) | | Air & Water Reactions | Hygroscopic. Sensitive to prolonged exposure to air. Water soluble. Reacts slowly with water. | | Reactivity Profile | A powerful reducing agent. Reacts with bases and oxidizing agents. | | Hazard | Toxic by ingestion, strong irritant to tissue. | | Fire Hazard | Flash point data for Hydroxylamine hydrochloride are not available; however, Hydroxylamine hydrochloride is probably combustible. | | Biochem/physiol Actions | MAO inhibitor; inhibits platelet aggregation. | | Contact allergens | Hydroxylamine and its salts are used in various
branches of industry, as reducing agents in color film
developers or as reagents in laboratories. | | Purification Methods | Crystallise the salt from aqueous75% ethanol or boiling methanol, and dry it under vacuum over CaSO4 or P2O5. It has also been dissolved in a minimum of water and saturated with HCl; after three such crystallisations, it is dried under a vacuum over CaCl2 and NaOH. Its solubility at 20o is 85% in H2O, 6% in EtOH and 12% in MeOH. [Hurd Inorg Synth I 87 1939, Semon in Org Synth Coll Vol I 318 1941.] |
| | Hydroxylamine hydrochloride Preparation Products And Raw materials |
| Raw materials | Sodium nitrite-->Dimethyl sulfate-->Water-->Sodium metabisulfite-->Nitromethane-->Acetone oxime | | Preparation Products | 2-AMINO-5,6-DICHLOROBENZOIC ACID-->ETHYL 5-METHYLISOXAZOLE-3-CARBOXYLATE-->5-METHYL-4-ISOXAZOLESULFONYL CHLORIDE-->5-AMINOISOXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER-->4-Aminotetrahydropyran hydrochloride-->6-Bromoisatin-->3,4,5-Trimethoxybenzylamine-->Methyl 3-amino-4-methylthiophene-2-carboxylate-->4-AMINO-1,2,5-OXADIAZOLE-3-CARBONITRILE-->3-(2,6-Dichlorophenyl)-5-methylisoxazole-4-carboxylic acid-->ETHYL 3-(2,6-DICHLORO-PHENYL)-5-METHYL-ISOXAZOLE-4-CARBOXYLATE-->Epiandrosterone acetate-->6-AMINO-2-METHYL-2-HEPTANOL-->5-Methyl-3-phenylisoxazole-->2,6-Dicyano-4-Nitroaniline-->(2,6-DIMETHYLPHENOXY)ACETOXIME-->2-Butanone oxime-->3-METHYL-5-PHENYL-4-ISOXAZOLECARBOXYLIC ACID-->4-(METHYLTHIO)BENZYLAMINE-->heptanal oxime-->3-(2-Chlorophenyl)-5-methylisoxazole-4-carbonyl chloride-->BENZAMIDOXIME HYDROCHLORIDE-->2-Pyridylamid oxime-->NEMONAPRIDE-->3-(2-Chlorophenyl)-5-methylisoxazole-4-carboxylic acid-->Adrafinil-->17-Ethinylandrost-5-ene-3,17-diol-->5-Methyl-3-phenylisoxazole-4-carbonyl chloride-->N'-HYDROXYPYRIDINE-4-CARBOXIMIDAMIDE-->3-PYRIDYLAMIDOXIME-->3-METHYL-5-PHENYLISOXAZOLE-->3-METHYLTHIOPHENE-2-CARBONITRILE-->N-Hydroxysulfosuccinimide sodium salt-->DIPHENYLGLYOXIME-->5-Chloro-3,6-dihydroxy-5-androstan-17-one 3-acetate-->2,3-DIMETHOXYBENZONITRILE-->5 A-CHLORO-6 B,19-EPOXY-3 B -HYDROXY-5 A-ANDROSTAN-17-ONE-->2-CHLOROBENZALOXIME-->Pyrazole-1,3-dimethyl-5-phenoxy-4-carboxaldehyde oxime-->Ethyl 5-methyl-3-phenylisoxazole-4-carboxylate |
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