2,5-Dihydroxybenzaldehyde
- Product Name
- 2,5-Dihydroxybenzaldehyde
- CAS No.
- 1194-98-5
- Chemical Name
- 2,5-Dihydroxybenzaldehyde
- Synonyms
- Gentisate aldehyde;GENTISALDEHYDE;NSC 72387;GENTISINALDEHYDE;Cyanohydroquinone;GENTISIC ALDEHYDE;ForMylhydroquinone;2,5-Dihydroxybenzald;5-HYDROXYSALICYLALDEHYDE;2,5-Dihydroxybenzaldchyde
- CBNumber
- CB7146305
- Molecular Formula
- C7H6O3
- Formula Weight
- 138.12
- MOL File
- 1194-98-5.mol
2,5-Dihydroxybenzaldehyde Property
- Melting point:
- 97-99 °C (lit.)
- Boiling point:
- 213.5°C (rough estimate)
- Density
- 1.2667 (rough estimate)
- refractive index
- 1.4797 (estimate)
- storage temp.
- Store below +30°C.
- solubility
- 13.8g/l soluble
- pka
- 8.89±0.18(Predicted)
- form
- Crystalline Powder
- color
- Yellow to khaki-green
- Water Solubility
- soluble
- Sensitive
- Air Sensitive
- BRN
- 1363961
- InChIKey
- CLFRCXCBWIQVRN-UHFFFAOYSA-N
- LogP
- 0.540
- CAS DataBase Reference
- 1194-98-5(CAS DataBase Reference)
- NIST Chemistry Reference
- 2,5-Dihydroxybenzaldehyde(1194-98-5)
- EPA Substance Registry System
- Benzaldehyde, 2,5-dihydroxy- (1194-98-5)
Safety
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-43
- Safety Statements
- 26-36/37/39-37/39-26,37/39-36
- WGK Germany
- 3
- Hazard Note
- Irritant
- TSCA
- Yes
- HS Code
- 29124990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H317May cause an allergic skin reaction
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- D108200
- Product name
- 2,5-Dihydroxybenzaldehyde
- Purity
- 98%
- Packaging
- 5g
- Price
- $166
- Updated
- 2024/03/01
- Product number
- D108200
- Product name
- 2,5-Dihydroxybenzaldehyde
- Purity
- 98%
- Packaging
- 25g
- Price
- $474.6
- Updated
- 2024/03/01
- Product number
- D0565
- Product name
- 2,5-Dihydroxybenzaldehyde
- Purity
- >98.0%(GC)
- Packaging
- 1g
- Price
- $27
- Updated
- 2024/03/01
- Product number
- D0565
- Product name
- 2,5-Dihydroxybenzaldehyde
- Purity
- >98.0%(GC)
- Packaging
- 5g
- Price
- $95
- Updated
- 2024/03/01
- Product number
- A15565
- Product name
- 2,5-Dihydroxybenzaldehyde, 98+%
- Packaging
- 1g
- Price
- $39.65
- Updated
- 2024/03/01
2,5-Dihydroxybenzaldehyde Chemical Properties,Usage,Production
Description
2,5-Dihydroxybenzaldehyde is a building block. It has been used in the synthesis of 2,4-dimethylbenzoylhydrazones with antileishmanial and antioxidant activity.
Chemical Properties
yellow to khaki-green crystalline powder
Uses
2,5-Dihydroxybenzaldehyde (cas# 1194-98-5) is a compound useful in organic synthesis.
Application
2,5-Dihydroxybenzaldehyde is a is a natural phenol found in the heartwoods of Pseudolarix amabilis, it is a tyrosine kinase inhibitor. 2,5-Dihydroxybenzaldehyde has antimicrobial activity and is mostly used in experimental studies for the preparation of Schiff base derivatives and bioanodes for glucose fuel cells.
Definition
ChEBI: 2,5-dihydroxybenzaldehyde is a dihydroxybenzaldehyde carrying hydroxy groups at positions 2 and 5. It has a role as a Penicillium metabolite, a mouse metabolite and a human metabolite.
Preparation
Add 80 mmol of dry paraformaldehyde to a mixture of 12 mmol of the phenol derivative and 2.5 mmol of MgO nanocrystalline (0.1 g). Expose the resulting mixture under microwave irradiation with a power of 650 W. Monitor the progress of the reaction by thin layer chromatography (TLC) developed by n-hexane : ethyl acetate (8 : 2). Add 100 mL of sulfuric acid (15% w/w) to the reaction mixture and heated at 50 °C for 15 min. Cool the reaction mixture to room temperature. Extract the product by dichloromethane (2 x 50 mL). Dry the organic layer over anhydrous magnesium sulphate. Evaporate the solution resulting from filtration to obtain the crude product. Purify the other product by column chromatography using n-hexane : ethyl acetate (95 : 5 to 70 : 30).
2,5-Dihydroxybenzaldehyde Preparation Products And Raw materials
Raw materials
Preparation Products
2,5-Dihydroxybenzaldehyde Suppliers
- Tel
- --
- Fax
- --
- info@trc-canada.com
- Country
- Canada
- ProdList
- 6038
- Advantage
- 71
View Lastest Price from 2,5-Dihydroxybenzaldehyde manufacturers
- Product
- 2,5-Dihydroxybenzaldehyde 1194-98-5
- Price
- US $999.00-666.00/ton
- Min. Order
- 1ton
- Purity
- 99%
- Supply Ability
- 5000
- Release date
- 2024-08-13
- Product
- 2,5-Dihydroxybenzaldehyde 1194-98-5
- Price
- US $750.00/KG
- Min. Order
- 1KG
- Purity
- 99
- Supply Ability
- 1000
- Release date
- 2024-04-18
- Product
- 2,5-Dihydroxybenzaldehyde 1194-98-5
- Price
- US $0.00-0.00/KG
- Min. Order
- 10mg
- Purity
- 99%HPLC
- Supply Ability
- 2000tons
- Release date
- 2020-01-15