Salicylaldoxime
- CAS No.
- 94-67-7
- Chemical Name:
- Salicylaldoxime
- Synonyms
- icyL;Saldox;doxime;Sal-dox;2-(βSalicyladoxime;SALICYLALDOXIME;SalicyladoximeGr;SALICYLADOXIME AR;Salicaldehyde oxime
- CBNumber:
- CB0112910
- Molecular Formula:
- C7H7NO2
- Molecular Weight:
- 137.14
- MDL Number:
- MFCD00002120
- MOL File:
- 94-67-7.mol
| Product description | Number | Pack Size | Price |
| Salicylaldoxime ≥98.0% (NT) | 84172 | 100g | $223 |
| Salicylaldoxime >98.0%(GC) | S0005 | 25g | $47 |
| Salicylaldoxime >98.0%(GC) | S0005 | 500g | $507 |
| Salicylaldoxime 98+% | 241941 | 25g | $163 |
| Salicylaldoxime | S881485 | 500mg | $60 |
| More product size | |||
| 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. |
| pka | pK1:1.37(＋1);pK2:9.18;pK3:12.11 (25°C) |
| form | Powder |
| 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) |  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 |
|
Salicylaldoxime price More Price(22)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | 84172 | Salicylaldoxime ≥98.0% (NT) | 94-67-7 | 100g | $223 | 2025-07-31 | Buy |
| TCI Chemical | S0005 | Salicylaldoxime >98.0%(GC) | 94-67-7 | 25g | $47 | 2025-07-31 | Buy |
| TCI Chemical | S0005 | Salicylaldoxime >98.0%(GC) | 94-67-7 | 500g | $507 | 2025-07-31 | Buy |
| Usbiological | 241941 | Salicylaldoxime 98+% | 94-67-7 | 25g | $163 | 2021-12-16 | Buy |
| TRC | S881485 | Salicylaldoxime | 94-67-7 | 500mg | $60 | 2021-12-16 | 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
90-02-8
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
Salicylaldoxime Preparation Products And Raw materials
Raw materials
1of2
Preparation Products
1of3
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Tangshan Moneide Trading Co., Ltd. | +86-315-8309571 +8615633399667 | sales@moneidechem.com | China | 574 | 58 |
| Hebei Chuanghai Biotechnology Co., Ltd | +8615350571055 | Sibel@chuanghaibio.com | China | 8753 | 58 |
| Shaanxi Dideu Medichem Co. Ltd | +86-29-81148696 +86-17392712697 | 1022@dideu.com | China | 3995 | 58 |
| Hebei Fengjia New Material Co., Ltd | +86-0311-87836622 +86-18712993135 | sales01@tairunfaz.com | China | 8051 | 58 |
| Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | info@tianfuchem.com | China | 21597 | 55 |
| career henan chemical co | +86-0371-86658258 +8613203830695 | sales@coreychem.com | China | 29831 | 58 |
| CONIER CHEM AND PHARMA LIMITED | +8618523575427 | sales@conier.com | China | 49977 | 58 |
| Antai Fine Chemical Technology Co.,Limited | 18503026267 | info@antaichem.com | CHINA | 9636 | 58 |
| TargetMol Chemicals Inc. | +1-781-999-5354; +17819995354 | marketing@targetmol.com | United States | 32470 | 58 |
| Hefei TNJ Chemical Industry Co.,Ltd. | +86-0551-65418671 +8618949823763 | sales@tnjchem.com | China | 34563 | 58 |
Related articles
- Salicylaldoxime: Applications in Solvent Extraction and Synthesis Method
- Salicylaldoxime, derived from salicylaldehyde and hydroxylamine, is vital in chemistry, medicine, and metallurgy, facilitating....
- Apr 11，2024
- Salicylaldoxime: activities, applications and safety
- Salicylaldoxime inhibits immune hemolysis and shows potential as a carbonic anhydrase inhibitor, but has safety concerns.
- Nov 14，2023
- What is Salicylaldoxime?
- Salicylaldoxime is an organic compound described by the formula C6H4CH=NOH-2-OH and it is the oxime of salicylaldehyde. This c....
- Jan 10，2020
View Lastest Price from Salicylaldoxime manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
 |
2026-01-30 | Salicylaldoxime
94-67-7
|
US $8.90 / KG | 1KG | 99% | 10 mt | Hebei Chuanghai Biotechnology Co., Ltd | |
 |
2026-01-05 | Salicylaldoxime
94-67-7
|
US $29.00 / mL | 99.97% | 10g | TargetMol Chemicals Inc. | ||
 |
2025-12-24 | Salicylaldoxime
94-67-7
|
US $0.00-0.00 / KG | 1KG | 99.0% | 1000KG | Shaanxi Dideu Medichem Co. Ltd |
-
- Salicylaldoxime
94-67-7
- US $8.90 / KG
- 99%
- Hebei Chuanghai Biotechnology Co., Ltd
-
- Salicylaldoxime
94-67-7
- US $29.00 / mL
- 99.97%
- TargetMol Chemicals Inc.
-
- Salicylaldoxime
94-67-7
- US $0.00-0.00 / KG
- 99.0%
- Shaanxi Dideu Medichem Co. Ltd
