Online Database of Chemicals from Around the World

delta-Valerolactone
[CAS# 542-28-9]

List of Suppliers
Simagchem Corporation China Inquire
www.simagchem.com
+86 13806087780
+86 (592) 268-0237
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink Standard supplier since 2008
Hefei TNJ Chemical Industry Co., Ltd. China Inquire
www.tnjchem.com
+86 (551) 6541-8684
+86 (551) 6541-8697
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink Standard supplier since 2010
Active biopharma Corp China Inquire
www.activebiopharma.com
+86 (571) 8161-2335
support@activebiopharma.com
Chemical manufacturer
chemBlink Standard supplier since 2012
Hangzhou Leap Chem Co., Ltd. China Inquire
www.leapchem.com
+86 (571) 8771-1850
market19@leapchem.com
QQ Chat
Chemical manufacturer since 2006
chemBlink Standard supplier since 2015
Hangzhou Molcore Biopharmatech Co., Ltd. China Inquire
www.molcore.com
+86 (571) 8102-5280
sales@molcore.com
QQ Chat
Chemical manufacturer since 2010
chemBlink Standard supplier since 2017
Myj Chemical Co., Ltd. China Inquire
www.myj2002.com
+86 15839353441
cflwjz@126.com
QQ Chat
Chemical manufacturer since 2002
chemBlink Standard supplier since 2021
Puyang Kaisheng Chemical Co., Ltd. China Inquire
www.pykshglookchem.com
+86 (0393) 698-6680
ashleywang2019@hotmail.com
Skype Chat
Chemical manufacturer since 2019
chemBlink Standard supplier since 2024
City Chemical LLC USA Inquire
www.citychemical.com
+1 (203) 932-2489
+1 (203) 937-8400
sales@citychemical.com
Chemical distributor
Alfa Aesar. USA Inquire
www.alfa.com
+1 (978) 521-6300
+1 (978) 521-6350
info@alfa.com
Chemical manufacturer
Whyte Chemicals UK Inquire
www.whytechemicals.co.uk
+44 (20) 8346-5946
+44 (20) 8349-4589
sales@whytechemicals.co.uk
Chemical distributor

Identification
ClassificationChemical reagent >> Organic reagent >> Ester >> Lactone compound
Namedelta-Valerolactone
SynonymsTetrahydro-2H-2-pyranone
Molecular StructureCAS # 542-28-9, delta-Valerolactone
Molecular FormulaC5H8O2
Molecular Weight100.12
CAS Registry Number542-28-9
EC Number208-807-1
SMILESC1CCOC(=O)C1
Properties
Density1.079
Melting point-13 °C
Boiling point230-60 °C
Refractive index1.456-1.459
Flash point112 °C
Water solubilitymiscible
Safety Data
Hazard Symbolssymbol   GHS05 Danger  Details
Risk StatementsH318  Details
Safety StatementsP264+P265-P280-P305+P354+P338-P317  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Serious eye damageEye Dam.1H318
Eye irritationEye Irrit.2H319
SDSAvailable
up Discovery and Applications
Delta-valerolactone (DVL) is a cyclic ester known for its diverse applications in chemical synthesis and industry. Its discovery and subsequent development have underscored its versatility as a chemical intermediate with significant industrial and commercial relevance.

Discovered in the mid-20th century, delta-valerolactone is a five-membered lactone derived from the condensation of gamma-hydroxybutyric acid (GHB). The synthesis of DVL involves the cyclization of 1,4-pentadiol or similar precursors, which forms the lactone ring structure. This process was initially explored to create compounds with specific reactivity profiles and potential uses in various chemical reactions.

In industrial applications, delta-valerolactone serves as an important intermediate in the production of various chemicals. One of its primary uses is in the synthesis of polyesters and resins. The lactone ring of DVL can be polymerized to form polymers with desirable mechanical properties and stability. These polymers find applications in coatings, adhesives, and other materials where durability and performance are critical.

Delta-valerolactone is also used as a solvent in chemical processes. Its ability to dissolve a range of organic compounds makes it valuable in the formulation of industrial solvents and cleaning agents. The solvent properties of DVL are particularly useful in formulations where a high degree of solvency and low toxicity are desired.

In the pharmaceutical industry, DVL is employed as a precursor in the synthesis of various drugs and therapeutic agents. Its ability to participate in ring-opening polymerization reactions allows for the creation of biologically active compounds with potential therapeutic benefits. Research into the applications of DVL in drug synthesis continues to explore its role in developing new medications and treatments.

Another notable application of delta-valerolactone is in the production of biodegradable materials. The polymerization of DVL can lead to the formation of biodegradable polymers, which are of increasing interest due to environmental concerns about plastic waste. These materials offer potential solutions for reducing the ecological impact of traditional plastics.

Despite its many applications, delta-valerolactone is relatively less well-known compared to other lactones and chemicals. However, its role in industrial chemistry and its potential for use in new materials and pharmaceuticals highlight its significance in various fields.

In summary, delta-valerolactone is a valuable chemical compound with a range of applications in industrial and pharmaceutical settings. Its role as an intermediate in polymer synthesis, solvent use, and the development of biodegradable materials demonstrates its versatility and importance in modern chemistry.

References

2024. New sustainable polymers with on-demand depolymerization property. Science China Chemistry.
DOI: 10.1007/s11426-024-2167-9

2024. Controllable Ring-opening Polymerization of δ-Valerolactone Catalyzed by Quinolinyl-Urea/MTBD Systems. Chinese Journal of Polymer Science.
DOI: 10.1007/s10118-024-3127-3

2023. Preparation of Chemically Recyclable Poly(ether-alt-ester) by the Ring Opening Polymerization of Cyclic Monomers Synthesized by Coupling Glycolide and Epoxides. Chinese Journal of Polymer Science, 41(11).
DOI: 10.1007/s10118-023-3040-1
Market Analysis Reports
List of Reports Available for delta-Valerolactone
Related Products
Valeric Acid De...  Valeric Acid 4-...  Valeric acid me...  Valeric Acid 2-...  Valeric Acid 4-...  Valeric Acid 2,...  Valeric anhydri...  Valeriotetrate ...  Valeriotriate B  gamma-Valerolac...  (R)-gamma-Valer...  Valeronitrile  Valeronitrile, ...  Valerophenone  Valerosidatum  2-Valerylbenzoi...  Valeryl chlorid...  4-Valeryl-4-(3-...  2-Valerylfuran  Valerylhydrazin...