Benzoin, 99%, Thermo Scientific Chemicals
Benzoin, 99%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Benzoin, 99%, Thermo Scientific Chemicals

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5000 g
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Catalog number A10188.0I
also known as A10188-0I
Price (USD)/ Each
378.65
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420.00 
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Quantity:
5000 g
Request bulk or custom format
Price (USD)/ Each
378.65
Online exclusive
420.00 
Save 41.35 (10%)
Add to cart
Benzoin, 99%, Thermo Scientific Chemicals
Catalog numberA10188.0I
Price (USD)/ Each
378.65
Online exclusive
420.00 
Save 41.35 (10%)
-
Add to cart
Chemical Identifiers
CAS119-53-9
SpecificationsSpecification SheetSpecification Sheet
Melting Point (clear melt)129-137?C
FormCrystals or powder or crystalline powder
Identification (FTIR)Conforms
Assay (GC)≥98.5%
Appearance (Color)White to cream or pale yellow
Benzoin is used as a flavor, antiseptic and photopolymerization catalyst. It is also used as a raw material in organic syntheses. It serves as a precursor to benzil, which is a photoinitiator. Further, it is used as degassing agent for powder coatings. In addition to this, it is used as an additive and in powder coating to remove the pinhole phenomenon.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Benzoin is used as a flavor, antiseptic and photopolymerization catalyst. It is also used as a raw material in organic syntheses. It serves as a precursor to benzil, which is a photoinitiator. Further, it is used as degassing agent for powder coatings. In addition to this, it is used as an additive and in powder coating to remove the pinhole phenomenon.

Solubility
Soluble in chlorine. Slightly soluble in water, ethanol and ether.

Notes
Moisture sensitive. Incompatible with acids, acid anhydrides, acid chlorides and strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Exclusive C-alkylation occurs with an alkyl bromide and NaOH in DMSO: Liebigs Ann. Chem., 735, 56 (1970). Borohydride reduction and periodate cleavage of the product lead to a useful synthesis of aryl ketones, with benzoin functioning as a benzoyl anion equivalent: Synthesis, 268 (1975):
  2. This has been extended to include alkylation with other electrophiles including primary and secondary alkyl iodides and Michael acceptors, and the route shortened by direct cleavage of the alkylated benzoin with hydrogen peroxide: Synthesis, 36 (1980).
  3. Zeng, H.; Wang, K.; Tian, Y.; Niu, Y.; Greene, L.; Hu, Z.; Lee, J. K. Reprint of The benzoin condensation: Charge tagging of the catalyst allows for tracking by mass spectrometry. Int. J. Mass Spectrom. 2015, 378, 169-174.
  4. Alamgir, M.; Khuhawar, M. Y.; Memon, S. Q.; Hayat, A.; Zounr, R. A. Spectrofluorimetric analysis of famotidine in pharmaceutical preparations and biological fluids by derivatization with benzoin. Spectrochim. Acta, Part A 2015, 134, 449-452.