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S607

Sigma-Aldrich

Salicylhydroxamic acid

99%

Synonym(s):

2-Hydroxybenzohydroxamic acid, N,2-Dihydroxybenzamide

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About This Item

Linear Formula:
HOC6H4CONHOH
CAS Number:
89-73-6
Molecular Weight:
153.14
EC Number:
201-934-3
MDL number:
MFCD00002110
UNSPSC Code:
12352100
PubChem Substance ID:
24899684
NACRES:
NA.22

Assay

99%

mp

177 °C (dec.) (lit.)

SMILES string

ONC(=O)c1ccccc1O

InChI

1S/C7H7NO3/c9-6-4-2-1-3-5(6)7(10)8-11/h1-4,9,11H,(H,8,10)

InChI key

HBROZNQEVUILML-UHFFFAOYSA-N

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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. 

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Metal complexes of salicylhydroxamic acid (H2Sha), anthranilic hydroxamic acid and benzohydroxamic acid. Crystal and molecular structure of [Cu (phen) 2 (Cl)] Cl . H2Sha, a model for a peroxidase-inhibitor complex
O'Brien EC, et al.
Journal of Inorganic Biochemistry, 79(1-4), 47-51 (2000)
A visualization method for studying the adsorption of lead species in salicylhydroxamic acid flotation of hemimorphite
Zhao W, et al.
Minerals Engineering, 154, 106434-106434 (2020)
Ayodeji S Owati et al.
Frontiers in plant science, 8, 1165-1165 (2017-07-18)
Ascochyta blight (AB) of pulse crops (chickpea, field pea, and lentils) causes yield loss in Montana, where 1.2 million acres was planted to pulses in 2016. Pyraclostrobin and azoxystrobin, quinone outside inhibitor (QoI) fungicides, have been the choice of farmers
Solomon Stonebloom et al.
Plant physiology, 158(1), 190-199 (2011-11-15)
Recent studies suggest that intercellular transport via plasmodesmata (PD) is regulated by cellular redox state. Until now, this relationship has been unclear, as increased production of reactive oxygen species (ROS) has been associated with both increased and decreased intercellular transport
Omer Murik et al.
The New phytologist, 221(3), 1303-1316 (2018-09-15)
Diatom dominance in contemporary aquatic environments indicates that they have developed unique and effective mechanisms to cope with the rapid and considerable fluctuations that characterize these environments. In view of their evolutionary history from a secondary endosymbiosis, inter-organellar regulation of
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