| Identification | More | [Name]
Salicylhydroxamic acid | [CAS]
89-73-6 | [Synonyms]
2-HYDROXYBENZHYDROXAMIC ACID
2-HYDROXYBENZOHYDROXAMIC ACID
AKOS BC-3099
IFLAB-BB F1918-0014
LABOTEST-BB LT00454000
N,2-DIHYDROXYBENZAMIDE
N-HYDROXYSALICYLAMIDE
SALICYLHYDROXAMIC ACID
SALICYLOHYDROXAMIC ACID
n,2-dihydroxy-benzamid
nsc5088
o-hydroxybenzohydroxamicacid
salicylohydroximicacid
sha
Salicylhydroxamicacid,99%
Salicylhydroxamic
Salicylhydroxomicacid
Salicylhydroxamic acid, 2-Hydroxybenzohydroxamic acid, Salicylhydroxyamide
2-Hydroxybenzohydroxamic acid, N,2-Dihydroxybenzamide
2-Hydroxybenzenehydroxamic acid | [EINECS(EC#)]
201-934-3 | [Molecular Formula]
C7H7NO3 | [MDL Number]
MFCD00002110 | [Molecular Weight]
153.14 | [MOL File]
89-73-6.mol |
| Chemical Properties | Back Directory | [Appearance]
off-white powder | [Melting point ]
177 °C (dec.) (lit.) | [Boiling point ]
276.03°C (rough estimate) | [density ]
1.3585 (rough estimate) | [refractive index ]
1.5500 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Fine Crystalline Powder | [pka]
pK (25°) 4.19 | [color ]
Beige-pink | [Stability:]
Stable. Incompatible with strong bases, strong oxidizing agents. Combustible. | [Water Solubility ]
It is soluble in water. | [Merck ]
14,8331 | [BRN ]
1210520 | [CAS DataBase Reference]
89-73-6(CAS DataBase Reference) | [EPA Substance Registry System]
89-73-6(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
R40:Limited evidence of a carcinogenic effect. | [Safety Statements ]
S22:Do not breathe dust .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
VO6870000
| [HS Code ]
29242990 |
| Hazard Information | Back Directory | [Chemical Properties]
Salicylhydroxamic acid(89-73-6) is a white needle crystal or off-white powder with a slow-heating melting point of 168°C. It is soluble in alcohol and ether and can be sublimated. When exposed to air, it progressively turns red. It is synthesized by combining methyl salicylate and hydroxylamine hydrochloride with sodium hydroxide, followed by acidification.
| [Uses]
Salicylhydroxamic acid is a collector with efficient chelating effect on rare metal oxide minerals. It is used in rare metal beneficiation and has the advantages of good selectivity and strong collecting power. Salicylhydroxamic acid is mainly used as a complexing agent or extractant for rare earth ore, copper oxide ore, lead-zinc oxide ore, gold ore, kaolin, etc., as well as organic synthesis intermediates. | [Application]
Salicylhydroxamic acid can be used:
To prepare phenylboronic acid-based bioconjugates for chromatographic applications.
As a ligand to synthesize Fe(III), Cu(II), Ni(II) and Zn(II) complexes.
As a selective collector in the segregation of oxide minerals using the flotation method. | [Definition]
ChEBI: A hydroxamic acid that is N-hydroxybenzamide carrying a phenolic hydroxy group at position 2. | [Preparation]
synthesis of salicylhydroxamic acid: The ligand was prepared in two steps, step one the methyl salicylate was prepared by the esterification of salicylic acid with methanol in this reaction 28g (0.2 mol) of salicylic acid, 81cm3 of methanol and 8cm3 of concentrated sulfuric acid were mixed and step two by the coupling reaction of hydroxylamine and methyl salicylate. 13.9 g (0.2mol) of hydroxyl amine was weighed and added to 200cm3 of 10% sodium hydroxide solution and cooled at room temperature. Then 152.3g (0.1mol) of methyl salicylate was added in small portions with vigorous shaking after each addition to ensure complete dissolution. The mixture was allowed to stand for 36 hours. Then it was acidified with2M sulphuricacid and cooled. The precipitate was filtered, recrystallized from hot water containing a drop of acetic acid, recooled and filtered; white precipitate collected and weighed, the yield was salicylhydroxamic acid(14g).
Preparation and Characterization of Salicylhydroxamic acid and its Complexes with Iron (III), Cobalt (II) and Manganese (II) | [Purification Methods]
Crystallise the hydroxamic acid from acetic acid. [Beilstein 10 H 98.] |
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