ChemFaces is a professional high-purity natural products manufacturer.
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1. Reference standards
2. Pharmacological research
3. Inhibitors
Benzaldehyde
Citing Use of our Products
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* Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock |
10 mM * 1 mL in DMSO / $7.0 / In-stock |
Other Packaging |
*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap |
More articles cited ChemFaces products.
Indian J Pharm Sci....2022...Asian J Beauty Cosmetol...2020...Anal Bioanal Chem....2020...Process Biochemistry2019, 87:213-220Chin J Appl. Physiol....2019...Evid Based Complement Alternat Me...2018...Int J Mol Sci.2021, 22(8):4211.BMC Plant Biol.2021, 21(1):60.
Nutrients.2018, 10(10)Pol J Microbiol.2021, 70(1):117-130.Phytother Res.2020, 34(4):788-795.The Japan Society for Analy. Chem...2017...Fitoterapia.2022, 157:105130.Toxicol In Vitro.2019, 59:161-178Int J Pharmacol2020, 16:1-9Cosmetics2021, 8(3),91.
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Our products had been exported to the following research institutions and universities, And still growing.
Universidad de Antioquia (Colombia)Florida International University (USA)China Medical University (Taiwan)Subang Jaya Medical Centre (Malaysia)
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Benzaldehyde
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manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Allergol Immunopathol (Madr).2022, 1;50(4):23-30.Food Research2022, 6(6): 30-38.Psychopharmacology (Berl).2020, 10.1007Heliyon.2023, e12778.Int J Mol Sci.2022, 23(20):12516. Heliyon2020, 6(6):e04337.Pharmacogn J.2022, 14(2):350-357Korean Journal of Pharmacognosy.2015, 46(4):352-364Evid Based Complement Alternat Med.2020, 2020:1970349.British Jou. Med.&Med. Research2014, 1802-1811
Related Screening Libraries
Size /Price /Stock |
10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
|
Related Libraries |
Phenols Compound Library |
Description: |
Reference standards. |
Benzaldehyde Description
Source: |
|
Solvent: |
Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc. |
Storage: |
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
|
After receiving: |
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling. |
ChemFaces New Products and Compounds
Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.
IF=13.297(2019)PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
1 mM |
9.4251 mL |
47.1254 mL |
94.2507 mL |
188.5014 mL |
235.6268 mL |
5 mM |
1.885 mL |
9.4251 mL |
18.8501 mL |
37.7003 mL |
47.1254 mL |
10 mM |
0.9425 mL |
4.7125 mL |
9.4251 mL |
18.8501 mL |
23.5627 mL |
50 mM |
0.1885 mL |
0.9425 mL |
1.885 mL |
3.77 mL |
4.7125 mL |
100 mM |
0.0943 mL |
0.4713 mL |
0.9425 mL |
1.885 mL |
2.3563 mL |
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Structure Identification: |
Journal of the American Chemical Society, 2008, 130(18):5854-5. | Size-SelectiveLewis Acid Catalysis in a Microporous Metal-Organic Framework with Exposed Mn 2+ Coordination Sites.[Reference: WebLink] | METHODS AND RESULTS:
Treatment of selected aldehydes and ketones with cyanotrimethylsilane in the presence of the microporous metal-organic framework Mn3[(Mn4Cl)3BTT8(CH3OH)10]2 (1, H3BTT = 1,3,5-benzenetristetrazol-5-yl) leads to rapid conversion to the corresponding cyanosilylated products. The transformation is catalyzed by coordinatively unsaturated Mn2+ ions that serve as Lewis acids and lead to conversion yields of 98 and 90% for Benzaldehyde and 1-naphthaldehyde, the highest thus far for a metal-organic framework. Larger carbonyl substrates cannot diffuse through the pores of 1, and conversion yields are much lower for these, attesting to the heterogeneity of the reaction and its dependence on guest size. The Mukaiyama-aldol reaction, known to require much more active Lewis catalysts, is also catalyzed in the presence of 1, representing the first such example for a metal-organic framework. Conversion yields obtained for the reaction of selected aldehydes with silyl enolates reach 63%, on par with those obtained with zeolites.
CONCLUSIONS:
Size selectivity is demonstrated for the first time with this reaction through the use of larger silyl enolate substrates. |
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