4-N-BUTOXYBENZALDEHYDE
- Product Name
- 4-N-BUTOXYBENZALDEHYDE
- CAS No.
- 5736-88-9
- Chemical Name
- 4-N-BUTOXYBENZALDEHYDE
- Synonyms
- NSC 508762;AKOS B000285;BUTOXYBENZALDEHYDE;TIMTEC-BB SBB008007;4-BUTOXYBENZALDEHYDE;4-butoxy-benzaldehyd;P-BUTOXYBENZALDEHYDE;OTAVA-BB BB7020401737;P-N-BUTOXYBENZALDEHYDE;4-N-BUTOXYBENZALDEHYDE
- CBNumber
- CB0149327
- Molecular Formula
- C11H14O2
- Formula Weight
- 178.23
- MOL File
- 5736-88-9.mol
4-N-BUTOXYBENZALDEHYDE Property
- Melting point:
- 184 °C
- Boiling point:
- 285 °C (lit.)
- Density
- 1.031 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.539(lit.)
- Flash point:
- >230 °F
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- Liquid
- Specific Gravity
- 1.031
- color
- Clear yellow to orang-red
- InChI
- InChI=1S/C11H14O2/c1-2-3-8-13-11-6-4-10(9-12)5-7-11/h4-7,9H,2-3,8H2,1H3
- InChIKey
- XHWMNHADTZZHGI-UHFFFAOYSA-N
- SMILES
- C1C=C(OCCCC)C=CC=1C=O
- CAS DataBase Reference
- 5736-88-9(CAS DataBase Reference)
- EPA Substance Registry System
- Benzaldehyde, 4-butoxy- (5736-88-9)
Safety
- Hazard Codes
- Xi,Xn
- Risk Statements
- 36/37/38-22
- Safety Statements
- 26
- WGK Germany
- 3
- TSCA
- Yes
- HazardClass
- IRRITANT
- HS Code
- 29124990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
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
- 238082
- Product name
- 4-Butoxybenzaldehyde
- Purity
- 98%
- Packaging
- 10g
- Price
- $199
- Updated
- 2025/07/31
- Product number
- B0126
- Product name
- 4-Butoxybenzaldehyde
- Purity
- >98.0%(GC)
- Packaging
- 25mL
- Price
- $153
- Updated
- 2025/07/31
- Product number
- B814148
- Product name
- 4-butoxybenzaldehyde
- Packaging
- 2.5mg
- Price
- $75
- Updated
- 2021/12/16
- Product number
- FB61818
- Product name
- 4-Butoxybenzaldehyde
- Packaging
- 50g
- Price
- $78
- Updated
- 2021/12/16
- Product number
- FB61818
- Product name
- 4-Butoxybenzaldehyde
- Packaging
- 100g
- Price
- $133
- Updated
- 2021/12/16
4-N-BUTOXYBENZALDEHYDE Chemical Properties,Usage,Production
Chemical Properties
CLEAR YELLOW TO ORANG-RED LIQUID
Uses
4-Butoxybenzaldehyde has been used in the synthesis of:
- 6-amino-4-(4-butoxyphenyl)-3,5-dicyanopyridine-2(1H)-thione
- 16-(p-butoxybenzylidene)androsta-1,4-diene-3,17-dione via condensation reaction with androsta-1,4-diene-3,17-dione
Synthesis Reference(s)
The Journal of Organic Chemistry, 66, p. 2966, 2001 DOI: 10.1021/jo0056848
General Description
Kinetic constant for the inhibition of the diphenolase activity of mushroom tyrosinase by 4-butoxybenzaldehyde has been evaluated.
Synthesis
109-65-9
123-08-0
5736-88-9
In a 100 mL round-bottomed flask equipped with a reflux condenser tube and a magnetic stirrer, p-hydroxybenzaldehyde (35 g, 287 mmol) and 1-bromobutane (30.92 mL, 287 mmol) were dissolved in N,N-dimethylformamide (DMF, 750 mL). The reaction mixture was stirred for 20 min under nitrogen protection. Subsequently, anhydrous potassium carbonate (118.83 g, 860 mmol) was added and the reaction was continued to be stirred at 70 °C for 20 hours. After completion of the reaction, the mixture was cooled to room temperature. The reaction was quenched with excess water and extracted with ethyl acetate. The organic phases were combined, washed several times with water, dried over anhydrous sodium sulfate and filtered. The crude product was purified by silica gel column chromatography (petroleum ether/ethyl acetate, 20:1) to afford the brown oily target product 4-butoxybenzaldehyde. Yield: 95%; 1H NMR (500 MHz, CDCl3) δH (ppm): 9.89 (s, 1H), 7.84 (d, J = 8.8 Hz, 2H), 7.00 (d, J = 8.6 Hz, 2H), 4.06 (t, J = 6.3 Hz, 2H), 1.79-1.85 (m, 2H), 1.49-1.57 (m. 2H), 1.01 (t, J = 7.3 Hz, 3H); 13C NMR (125 MHz, CDCl3) δC (ppm): 190.7, 164.2, 131.9, 129.8, 114.7, 68.1, 31.0, 19.1, 13.7; ESI-MS: m/z 179.2 ([M + H]+). The following alkoxybenzaldehyde derivatives 4b-h were synthesized by a similar method.
References
[1] Journal of the American Chemical Society, 2014, vol. 136, # 46, p. 16399 - 16410
[2] Journal of the American Chemical Society, 2010, vol. 132, # 39, p. 13675 - 13683
[3] European Journal of Medicinal Chemistry, 2017, vol. 130, p. 286 - 307
[4] Synthetic Communications, 2001, vol. 31, # 21, p. 3323 - 3328
[5] Patent: CN107556333, 2018, A. Location in patent: Paragraph 0076-0079
4-N-BUTOXYBENZALDEHYDE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 4-N-BUTOXYBENZALDEHYDE manufacturers
- Product
- 4-N-BUTOXYBENZALDEHYDE 5736-88-9
- Price
- US $0.00-0.00/KG
- Min. Order
- 1KG
- Purity
- 98%
- Supply Ability
- 1ton
- Release date
- 2022-10-14
- Product
- 4-Butoxybenzaldehyde 5736-88-9
- Price
- US $0.00-0.00/g
- Min. Order
- 10mg
- Purity
- 99%HPLC
- Supply Ability
- 2000tons
- Release date
- 2020-01-15
- Product
- 4-N-BUTOXYBENZALDEHYDE 5736-88-9
- Price
- US $15.00-10.00/KG
- Min. Order
- 1KG
- Purity
- 99%+ HPLC
- Supply Ability
- Monthly supply of 1 ton
- Release date
- 2021-08-10