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Salicylhydroxamic acid, 99%

CAS: 89-73-6 | C7H7NO3 | 153.137 g/mol

$68.18 - $386.56

Chemical Identifiers

CAS 89-73-6
Molecular Formula C7H7NO3
Molecular Weight (g/mol) 153.137
MDL Number MFCD00002110
InChI Key HBROZNQEVUILML-UHFFFAOYSA-N
Synonym salicylhydroxamic acid, 2-hydroxybenzohydroxamic acid, salicylohydroxamic acid, sham, salicylohydroximic acid, benzamide, n,2-dihydroxy, 2-hydroxybenzhydroxamic acid, o-hydroxybenzohydroxamic acid, sha, 2,n-dihydroxy-benzamide
PubChem CID 66644
ChEBI CHEBI:45615
IUPAC Name N,2-dihydroxybenzamide
SMILES C1=CC=C(C(=C1)C(=O)NO)O
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Products 4
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AAA1152809
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Thermo Scientific Chemicals
A1152809
10 g
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AAA1152814
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Thermo Scientific Chemicals
A1152814
25 g
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AAA1152818
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A1152818
50 g
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AAA1152822
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A1152822
100 g
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Description

Description

It is widely used for a variety of roles in biology and medicine as a chelating therapy. It inhibits bacterial or fungi growth by interfering with iron uptake. It is also active as a inhibitor of enzyme involved in tumour growths. These compounds are used as extractants for the separation of valuable metals or minerals including copper, lead, gold, other rare earth metals and kaolin. Hydroxamic acids are also used to produce corresponding isocyanates by dehydration followed by rearrangement reaction. It is also used as a common ligand utilized in the synthesis of metallacrowns.

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
It is widely used for a variety of roles in biology and medicine as a chelating therapy. It inhibits bacterial or fungi growth by interfering with iron uptake. It is also active as a inhibitor of enzyme involved in tumour growths. These compounds are used as extractants for the separation of valuable metals or minerals including copper, lead, gold, other rare earth metals and kaolin. Hydroxamic acids are also used to produce corresponding isocyanates by dehydration followed by rearrangement reaction. It is also used as a common ligand utilized in the synthesis of metallacrowns.

Solubility
It is soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible to Strong bases. Stable under normal conditions.
Specifications

Chemical Identifiers

89-73-6
153.137
HBROZNQEVUILML-UHFFFAOYSA-N
66644
N,2-dihydroxybenzamide
C7H7NO3
MFCD00002110
salicylhydroxamic acid, 2-hydroxybenzohydroxamic acid, salicylohydroxamic acid, sham, salicylohydroximic acid, benzamide, n,2-dihydroxy, 2-hydroxybenzhydroxamic acid, o-hydroxybenzohydroxamic acid, sha, 2,n-dihydroxy-benzamide
CHEBI:45615
C1=CC=C(C(=C1)C(=O)NO)O

Specifications

89-73-6
C7H7NO3
10 g
14,8331
It is soluble in water.
C1=CC=C(C(=C1)C(=O)NO)O
153.137
CHEBI:45615
99%
∼170°C (decomposition)
MFCD00002110
1210520
salicylhydroxamic acid, 2-hydroxybenzohydroxamic acid, salicylohydroxamic acid, sham, salicylohydroximic acid, benzamide, n,2-dihydroxy, 2-hydroxybenzhydroxamic acid, o-hydroxybenzohydroxamic acid, sha, 2,n-dihydroxy-benzamide
HBROZNQEVUILML-UHFFFAOYSA-N
N,2-dihydroxybenzamide
66644
153.14
Salicylhydroxamic acid
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Safety and Handling

Safety and Handling

GHS H Statement
H341-H315-H319-H335
Suspected of causing genetic defects.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P201-P202-P261-P264b-P271-P280i-P281-P302+P352-P304+P340-P305+P351+P338-P308+P313-P332+P313-P362-P501c

H315-H319-H335-H341

EINECSNumber : 201-934-3

RTECSNumber : VO6870000

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only