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1-Naphthaldehyde, 2-hydroxy-

2-Hydroxy-1-naphthaldehyde

CAS: 708-06-5

Molecular Formula: C11H8O2

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1-Naphthaldehyde, 2-hydroxy- - Names and Identifiers

Name 2-Hydroxy-1-naphthaldehyde
Synonyms TIMTEC-BB SBB003835
1-Formyl-2-naphthol
2-Hyroxy-1-Naphthyldhyd
2-Hydroxy-1-phthaldehyde
2-hydroxy-1-naphthaldehyd
2-Hydroxy-1-naphthaldehyde
2-Hydroxy-1-naphthalaldehyde
1-Naphthaldehyde, 2-hydroxy-
1-formyl-2-hydroxynaphthalene
1-Formyl-2-hydroxy-naphthalene
1-Hydroxy-2-naphthalenecarboxaldehyde
CAS 708-06-5
EINECS 211-902-0
InChI InChI=1/C11H8O2/c12-7-10-9-4-2-1-3-8(9)5-6-11(10)13/h1-7,13H

1-Naphthaldehyde, 2-hydroxy- - Physico-chemical Properties

Molecular FormulaC11H8O2
Molar Mass172.18
Density1.1153 (rough estimate)
Melting Point76-80 °C (lit.)
Boling Point192 °C/27 mmHg (lit.)
Flash Point191-193°C/27mm
Water SolubilitySoluble in water (40 g/L at 20°C).
Solubility Chloroform, Methanol
Vapor Presure0.002Pa at 20℃
AppearanceCrystalline powder
ColorYellow
BRN742777
pKa8.27±0.50(Predicted)
Storage ConditionKeep in dark place,Sealed in dry,Room Temperature
SensitiveAir Sensitive
Refractive Index1.5500 (estimate)
MDLMFCD00004005
Physical and Chemical PropertiesColorless needle-like or prismatic crystals. The melting point of 82 deg C, boiling point of 192 deg C (3.6kPa). Soluble in ethanol, ether and petroleum, insoluble in water, soluble in aqueous alkali solution, soluble in concentrated sulfuric acid yellow. Slightly volatile in the steam, iron chloride Brown. Preparation Method: from 2-naphthol and chloroform reaction derived. Ethanol and 2-naphthol were added to the reaction pot, and the mixture was heated to 40 ° C. And stirred for 0.5 hours. Then 30% sodium hydroxide solution was added, and the temperature was raised to 75 °c. Chloroform was added dropwise to control the reaction temperature to 78 °c. After the addition, the temperature was maintained at 78 °c for 2H. Then, the temperature was raised to 90 ° C., and ethanol and excess chloroform were distilled off. After steaming, the mixture was cooled to below 30 ° C., and allowed to stand for 6 hours. The filtrate was filtered, stirred with water, heated to 60 °c and neutralized with hydrochloric acid to a pH of 2-3. Cooling, filtration, drying of the filter cake below 60 °c, to obtain the finished product. Purposes: the product is an intermediate in organic synthesis, but also for the determination of palladium, beryllium Analytical reagents. The fluorescent whitening agent PEB can be synthesized by the ring formation of 2-hydroxy-1-naphthalene formaldehyde and diethyl malonate in the presence of acetic anhydride. Add 28 kg2-hydroxy -1-naphthalene formaldehyde, 29kg of diethyl malonate and 50kg of acetic anhydride into the reaction pot, stir, heat to 130 ℃, Reflux 8H. Heating was stopped and stirring was continued for 1H. It was cooled to 80 °c and allowed to stand for 24h. Filter with suction, wash the cake with 10% soda ash solution, and then wash the cake to Neutral with clear water. The filter cake was then added to 40kg of alcohol and dissolved by heating. Cooling, filtration. The filter cake was washed with a small amount of ethanol, dried at 60 ° C., and pulverized to obtain a standard of 36kg of fluorescent whitening agent PEB. The fluorescent whitening agent PEB is mainly used for the whitening of white materials such as selurolo White Material, polyvinyl chloride, acetic acid fiber and the brightening of coloring materials.
UseUsed as dye, fluorescent whitening agent Intermediate

1-Naphthaldehyde, 2-hydroxy- - Risk and Safety

Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
S60 - This material and its container must be disposed of as hazardous waste.
S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. 
S24/25 - Avoid contact with skin and eyes.
S37 - Wear suitable gloves.
UN IDsUN 3077 9/PG 3
WGK Germany2
RTECSQJ0300000
TSCAYes
HS Code29124990
Hazard Class9

1-Naphthaldehyde, 2-hydroxy- - Reference Information

LogP6 at 23℃ and pH8
NIST chemical information information provided by: webbook.nist.gov (external link)
EPA chemical substance information information provided by: ofmpeb.epa.gov (external link)
purpose This product is an intermediate in organic synthesis and an analytical reagent for the determination of palladium and beryllium. The fluorescent whitening agent PEB can be synthesized by the ring formation of 2-hydroxy-1-naphthalene formaldehyde and diethyl malonate in the presence of acetic anhydride. 28kg of 2-hydroxy-1-naphthalene formaldehyde, 29kg of diethyl malonate and 50kg of acetic anhydride were added into the reaction pot, stirred, heated to 130 ° C., and refluxed for 8 hours. Heating was stopped and stirring was continued for 1H. It was cooled to 80 °c and allowed to stand for 24h. Filter with suction, wash the cake with 10% soda ash solution, and then wash the cake to Neutral with clear water. The filter cake was then added to 40kg of alcohol and dissolved by heating. Cooling, filtration. The filter cake was washed with a small amount of ethanol, dried at 60 ° C., and pulverized to obtain a standard of 36kg of fluorescent whitening agent PEB. The fluorescent whitening agent PEB is mainly used for the whitening of white materials such as selurolo White Material, polyvinyl chloride, acetic acid fiber and the brightening of coloring materials.
used as intermediate of dye and fluorescent brightener
production method results from the reaction of 2-naphthol with chloroform. Ethanol and 2-naphthol were added to the reaction pot, and the mixture was heated to 40 ° C. And stirred for 0.5 hours. Then 30% sodium hydroxide solution was added, and the temperature was raised to 75 °c. Chloroform was added dropwise to control the reaction temperature to 78 °c. After the addition, the temperature was maintained at 78 °c for 2H. Then, the temperature was raised to 90 ° C., and ethanol and excess chloroform were distilled off. After steaming, the mixture was cooled to below 30 ° C., and allowed to stand for 6 hours. The filtrate was filtered, stirred with water, heated to 60 °c and neutralized with hydrochloric acid to a pH of 2-3. Cooling, filtration, drying of the filter cake below 60 °c, to obtain the finished product. Purposes: the product is an intermediate in organic synthesis, but also for the determination of palladium, beryllium Analytical reagents. The fluorescent whitening agent PEB can be synthesized by the ring formation of 2-hydroxy-1-naphthalene formaldehyde and diethyl malonate in the presence of acetic anhydride. 28kg of 2-hydroxy-1-naphthalene formaldehyde, 29kg of diethyl malonate and 50kg of acetic anhydride were added into the reaction pot, stirred, heated to 130 ° C., and refluxed for 8 hours. Heating was stopped and stirring was continued for 1H. It was cooled to 80 °c and allowed to stand for 24h. Filter with suction, wash cake with 10% soda ash solution, The filter cake was then washed with clear water until neutral. The filter cake was then added to 40kg of alcohol and dissolved by heating. Cooling, filtration. The filter cake was washed with a small amount of ethanol, dried at 60 ° C., and pulverized to obtain a standard of 36kg of fluorescent whitening agent PEB. The fluorescent whitening agent PEB is mainly used for the whitening of white materials such as selurolo White Material, polyvinyl chloride, acetic acid fiber and the brightening of coloring materials.
Last Update:2024-04-09 21:11:58
1-Naphthaldehyde, 2-hydroxy-
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View History
1-Naphthaldehyde, 2-hydroxy-
Methanone, (2,3,5,6-tetramethyl-1,4-phenylene)bis[(4-aminophenyl)- (9CI)
反-2-,顺-6-壬二烯醛
1,2-乙二胺与氮丙啶的聚合物
2-[(4-氯苯基)(吡啶-2-基)甲氧基]-N,N-二甲基乙胺
无水氨噻肟酸
四氟代硼酸根
NICOTINAMIDE CHLOROMETHYLATE
4,4'-BIS(2-AMINO-6-METHYLPYRIMIDYL) DISULFIDE
(2-溴-4-甲基苯基)甲醇
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