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2-Benzyloxy-1,3-propanediol (CAS 14690-00-7)

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Alternate Names:
2-(Phenylmethoxy)-1,3-propanediol; 2-O-Benzylglycerol
Application:
2-Benzyloxy-1,3-propanediol is a gylcerol derivative used in the preparation of glycerides
CAS Number:
14690-00-7
Molecular Weight:
182.22
Molecular Formula:
C10H14O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Benzyloxy-1,3-propanediol is a synthetic organic compound notable for its unique structural features that include a benzyl ether group attached to a glycerol backbone. This structure makes it an interesting subject for chemical research, particularly in the synthesis of more complex organic molecules. Its presence in synthetic chemistry is crucial for the development of novel organic synthesis methodologies that often require protected forms of glycerol. The benzyl group in 2-Benzyloxy-1,3-propanediol acts as a protecting group, making the hydroxyl groups less reactive and thus easier to work with in multi-step synthetic procedures. This feature is especially valuable in the synthesis of various pharmaceutical and fine chemical intermediates where selective reactivity is necessary. Additionally, the molecule finds use in studies involving the cleavage of ether bonds, providing insights into reaction mechanisms and kinetics in organic chemistry. In materials science, this compound has been explored for its potential in creating polymers and resins with specific properties such as improved durability and chemical resistance.


2-Benzyloxy-1,3-propanediol (CAS 14690-00-7) References

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  2. Central depressant and anticonvulsant properties of glycerol ethers isomeric with mephenesin.  |  BERGER, FM. 1952. J Pharmacol Exp Ther. 105: 450-7. PMID: 14955775
  3. Synthesis and characterization of biodegradable poly(ethylene glycol)-block-poly(5-benzyloxy-trimethylene carbonate) copolymers for drug delivery.  |  Zeng, F., et al. 2004. Biomacromolecules. 5: 1810-7. PMID: 15360292
  4. Synthesis and characterization of novel biotinylated biodegradable poly(ethylene glycol)-b-poly(carbonate-lactic acid) copolymers.  |  Xie, Z., et al. 2005. Acta Biomater. 1: 635-41. PMID: 16701844
  5. Conjugates of 1,3- and 1,2-Acylglycerols with Stigmasterol: Synthesis, NMR Characterization, and Impact on Lipid Bilayers.  |  Gładkowski, W., et al. 2023. Chempluschem. 88: e202300161. PMID: 36997498
  6. Synthesis and characterization of novel aliphatic polycarbonates[J].  |  Wang X L, Zhuo R X, Liu L J. 2002,. Journal of Polymer Science Part A: Polymer Chemistry,. 40(1):: 70-75.
  7. Synthesis of short and long chain cardiolipins[J].  |  Ali S M, Ahmad M U, Koslosky P. 2006,. Tetrahedron,. 62(29):: 6990-6997.
  8. Synthesis of functionalizable and biodegradable polymers via ring‐opening polymerization of 5‐benzyloxy‐trimethylene carbonate and ε‐caprolactone[J].  |  Lai K L, Ji L J, Long C Y,., 2012. Journal of applied polymer science., 123(4):: 2204-2210.
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Benzyloxy-1,3-propanediol, 100 mg

sc-391718
100 mg
$320.00