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Salicylaldoxime

CAS No.
94-67-7
Chemical Name:
Salicylaldoxime
Synonyms
(E)-2-hydroxybenzaldehyde oxiMe;icyL;doxime;Saldox;Sal-dox;2-(βSalicyladoxime;SALICYLALDOXIME;SalicyladoximeGr;SALICYLADOXIME AR
CBNumber:
CB0112910
Molecular Formula:
C7H7NO2
Molecular Weight:
137.14
MDL Number:
MFCD00002120
MOL File:
94-67-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-25 20:17:46
Product description Number Pack Size Price
Salicylaldoxime ≥98.0% (NT) 84172 100g $237
Salicylaldoxime >98.0%(GC) S0005 25g $47
Salicylaldoxime >98.0%(GC) S0005 500g $507
Salicylaldoxime Asreported 289060 50g $340
Salicylaldoxime Asreported 289060 100g $460
More product size

Salicylaldoxime Properties

Melting point 57-59 °C 59-61 °C (lit.)
Boiling point 251.96°C (rough estimate)
Density 1.2528 (rough estimate)
refractive index 1.5030 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility sparingly soluble in water, soluble in ethanol, diethyl ether, acetone, benzene.
form Powder
pka pK1:1.37(+1);pK2:9.18;pK3:12.11 (25°C)
color Bordeaux to purple-red
Odor Odorless
Water Solubility Slightly soluble in water
Merck 14,8327
BRN 1859881
InChI 1S/C7H7NO2/c9-7-4-2-1-3-6(7)5-8-10/h1-5,9-10H/b8-5+
InChIKey ORIHZIZPTZTNCU-VMPITWQZSA-N
SMILES O\N=C\c1ccccc1O
CAS DataBase Reference 94-67-7(CAS DataBase Reference)
FDA UNII 2QTV2A0T5Q
NIST Chemistry Reference Benzaldehyde, 2-hydroxy-, oxime(94-67-7)
EPA Substance Registry System Benzaldehyde, 2-hydroxy-, oxime (94-67-7)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P301+P312+P330-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn,Xi
Risk Statements  22-36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  VN5775000
TSCA  TSCA listed
HazardClass  IRRITANT
HS Code  29280000
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

Salicylaldoxime price More Price(57)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 84172 Salicylaldoxime ≥98.0% (NT) 94-67-7 100g $237 2026-04-30 Buy
TCI Chemical S0005 Salicylaldoxime >98.0%(GC) 94-67-7 25g $47 2026-04-30 Buy
TCI Chemical S0005 Salicylaldoxime >98.0%(GC) 94-67-7 500g $507 2026-04-30 Buy
Usbiological 289060 Salicylaldoxime Asreported 94-67-7 50g $340 2026-06-03 Buy
Usbiological 289060 Salicylaldoxime Asreported 94-67-7 100g $460 2026-06-03 Buy
Product number Packaging Price Buy
84172 100g $237 Buy
S0005 25g $47 Buy
S0005 500g $507 Buy
289060 50g $340 Buy
289060 100g $460 Buy

Salicylaldoxime Chemical Properties,Uses,Production

Uses

Salicylaldoxime is an organic compound described by the formula C6H4CH=NOH-2-OH and it is the oxime of salicylaldehyde. This crystalline, colorless solid is a chelator and sometimes used in the analysis of samples containing transition metal ions, with which it often forms brightly colored coordination complexes.

Elements Extraction

Salicylaldoxime is recognized as a selective precipitant for copper, although it forms water-insoluble chelates with a number of elements. Ingvar Dahl invested the extraction of divalent magnesium, manganese, cobalt, nickel, copper, zinc, cadmium, mercury, and lead with solutions of salicylaldoxime in benzene and the effect of the reagent concentration and particularly the pH of the aqueous phase on the extractability was also studied. The solubility of salicylaldoxime in organic solvents has been utilized in the solvent extraction of carious elements.

Chemical Properties

off-white to light beige crystalline powder

Uses

As a reagent for copper and nickel.

Uses

Salicylaldoxime reacts with several metal ions to give intensively coloured complexes which are insoluble in water. The structure of the copper(II), nickel(II) and palladium(II) complexes is shown in Fig. 14 (structure I), and that of the manganese(II), iron(II), cobalt(II) and zinc(II) complexes in Fig. 14 (structure II). The copper(Il) and palladium(II) salicylaldoxime complexes are of importance from an analytical point of view. The complexes precipitated from aqueous media are easily filterable and washable and are weighed after drying at 100°C. The precipitates are of stoichiometric composition.
The outstanding stabilities of the copper(II) and palladium(II) complexes make the reagent suitable for the selective determination of these metal ions. These two complexes form quantitatively at low pH values where the complexes of other metal ions do not exist.
Besides the gravimetric method, salicylaldoxime is also useful in the volumetric, amperometric and nephelometric determinations of copper and palladium.
Salicylaldoxime gives a black precipitate with VOs~ in media containing sulfuric acid; this is soluble in chloroform to give an orange solution. The reaction is specific for vanadium which can thus be detected by this method in the presence of almost all other metals.
In neutral medium salicylaldoxime reacts with iron(III) to give a red complex which is soluble in water. The reaction is utilized for the detection of micro amounts of iron.

Synthesis

Salicylaldehyde

90-02-8

Salicylaldoxime

94-67-7

The general procedure for the synthesis of salicylaldehyde oxime from salicylaldehyde is as follows: 30 mmol of 2-hydroxybenzaldehyde, 60 mmol of sodium bicarbonate, and 45 mmol of hydroxylamine hydrochloride were dissolved in a mixed ethanol/water solvent (50 mL of ethanol/5 mL of water) at room temperature. The reaction mixture was stirred for 2 hours, followed by removal of most of the solvent by concentration. The residue was diluted with ethyl acetate and filtered directly. The filtrate was concentrated to give a final 3.99 g (98% yield) of the colorless oily product salicylaldoxime.

References

[1] Journal fuer Praktische Chemie (Leipzig), 1989, vol. 331, # 5, p. 870 - 872
[2] Journal of the Iranian Chemical Society, 2010, vol. 7, # 1, p. 114 - 118
[3] Patent: CN103864754, 2016, B. Location in patent: Paragraph 0378; 0379
[4] Chemical Communications, 2014, vol. 50, # 56, p. 7531 - 7534
[5] Revue Roumaine de Chimie, 2015, vol. 60, # 9, p. 875 - 880

90-02-8
94-67-7
Synthesis of Salicylaldoxime from Salicylaldehyde
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View Lastest Price from Salicylaldoxime manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Salicylaldoxime pictures 2026-07-15 Salicylaldoxime
94-67-7
$29.00 99.97% 10g TargetMol Chemicals Inc.
Salicylaldoxime pictures 2026-03-20 Salicylaldoxime
94-67-7
$8.90 1KG 99% 10 mt Hebei Chuanghai Biotechnology Co., Ltd
Salicylaldoxime pictures 2025-12-24 Salicylaldoxime
94-67-7
1KG 99.0% 1000KG Shaanxi Dideu Medichem Co. Ltd
LABOTEST-BB LT00000132 SALICYLALDEHYDE OXIME SALICYLALDOXIME 2-HYDROXYBENZALDEHYDE OXIME SALICYLALDOXIME / 2-HYDROXYBENZALDEHYDE OXIME SalicylaldoxiMe, 98% 100GR SalicylaldoxiMe, 98% 25GR SalicylaldoxiMe >=98.0% (NT) doxime icyL SALICYLALDOXIME R. G. SALICYLALDOXIME, REAGENT GRADE SalicyladoximeGr Salicylaldoxime,98+% Benzaldehyde,2-hydroxy-,oxime o-Hydroxybenzaldehyde oxime o-hydroxybenzaldehydeoxime o-Hydroxybenzaldoxime Saldox Sal-dox Salicaldehyde oxime Salicylaldehydoxime (2-Hydroxyphenylmethylene)azanol 2-hydroxy-benzaldehydoxime 2-Hydroxybenzaldoxime Salicyladoxime 2-Hydroxy-benzaldehyde oxime Salicylaldoxime Salicylaldo94-67-7xime Salicylaldoxime > Salicylaldoxime, GR 98%+ SALICYLADOXIME AR 2-(β -D-glucopyranosyloxy)benzaldehyde Salicylaldoxime, 10 mM in DMSO (E)-2-hydroxybenzaldehyde oxiMe 94-67-7 94-67-6 HOC6H4CHNOH 2HOC6H4CHNOH C7F7NO2 Building Blocks Oximes Nitrogen Compounds Organic Building Blocks Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes