Page last updated: 2024-12-06

1,3-pentadiene

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

## 1,3-Pentadiene: A Versatile Research Tool

1,3-Pentadiene is a conjugated diene, meaning it has two double bonds separated by a single bond. This specific molecule is a colorless liquid with a pungent odor, and its chemical formula is C5H8.

**Why is 1,3-Pentadiene important for research?**

1,3-Pentadiene's importance stems from its unique properties and versatile applications in various fields, including:

**1. Polymer Chemistry:**

* **Diels-Alder Reactions:** 1,3-Pentadiene is a common diene in Diels-Alder reactions, a powerful tool for synthesizing cyclic compounds. This reaction is fundamental in organic chemistry and finds applications in pharmaceuticals, polymers, and natural product synthesis.
* **Polymerization:** 1,3-Pentadiene can undergo polymerization to form polymers with unique properties. These polymers are valuable in the development of new materials with specific characteristics like elasticity, strength, and resistance to heat.

**2. Spectroscopic Studies:**

* **NMR Spectroscopy:** 1,3-Pentadiene exhibits specific NMR signals that can be used to study molecular structure and dynamics. These signals are valuable for understanding the behavior of conjugated dienes in different environments.
* **IR Spectroscopy:** The characteristic vibrational frequencies of 1,3-pentadiene in IR spectroscopy are used to identify and quantify the molecule in complex mixtures.

**3. Theoretical Chemistry:**

* **Computational Chemistry:** 1,3-Pentadiene serves as a model system for theoretical calculations and simulations of conjugated dienes. These calculations help understand the electronic structure, reactivity, and spectroscopic properties of these important molecules.

**4. Catalytic Studies:**

* **Catalysis:** 1,3-Pentadiene is often used as a probe molecule to study the activity and selectivity of catalysts. Its reactivity in different catalytic processes can provide insight into the mechanisms of catalysis and the design of new catalysts.

**5. Other Applications:**

* 1,3-Pentadiene is also used in the production of other chemicals, including pharmaceuticals, pesticides, and fragrances.

In conclusion, 1,3-pentadiene is a versatile molecule with numerous applications in diverse fields. Its unique properties, particularly its conjugated diene structure, make it a valuable tool for research in areas like polymer chemistry, spectroscopy, theoretical chemistry, and catalysis. This molecule continues to play a significant role in advancing our understanding of chemistry and its applications.

1,3-pentadiene: a linear 5-carbon alkene; RN given refers to cpd with unspecified isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

(E)-1,3-pentadiene : An alkadiene consisting of pentane with the two double bonds located at positions 1 and 3. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID62204
CHEBI ID74165
MeSH IDM0058647

Synonyms (59)

Synonym
BB 0262541
1,3-pentadiene, (e)-
1,3-pentadiene
504-60-9
trans-penta-1,3-diene
1-methylbutadiene
pentadiene, 1,3-
rcra waste no. u186
piperylene
einecs 217-909-5
ccris 8964
nsc 73901
brn 1523657
hsdb 6139
rcra waste number u186
brn 1523659
hsdb 6063
einecs 207-995-2
trans-1,3-pentadiene
1,trans-3-pentadiene
2004-70-8
trans-piperylene
(e)-1,3-pentadiene
nsc-73901
nsc73901
trans-1-methylbutadiene
(3e)-penta-1,3-diene
1,3-pentadiene, (3e)-
trans-1,3-pentadiene, 90%
P1841
P0647
41050-31-1
4-01-00-00994 (beilstein handbook reference)
unii-00oa1gpf8r
00oa1gpf8r ,
68308-15-6
pentadiene
unii-fw963nf88b
fw963nf88b ,
4-01-00-00995 (beilstein handbook reference)
ec 207-995-2
CHEBI:74165
(e)-ch2=chch=chch3
AKOS015913480
(e)-piperylene
trans-1-methyl-1,3-butadiene
piperylene, trans-
1,3-trans-pentadiene
1,3-pentadiene (3e)-form [mi]
(3e)-1,3-pentadiene
trans-1,3-pentadiene (stabilized with tbc)
e-1, 3-pentadiene
e-1,3-pentadiene
ch2=chch=chch3
DTXSID50858710
trans-1,3-pentadiene, analytical standard
J-012974
(e)-penta-1,3-diene
Q126292
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
alkadieneAcyclic branched or unbranched hydrocarbons having two carbon-carbon double bonds.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (21)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (9.52)18.7374
1990's1 (4.76)18.2507
2000's5 (23.81)29.6817
2010's11 (52.38)24.3611
2020's2 (9.52)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 55.23

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index55.23 (24.57)
Research Supply Index3.14 (2.92)
Research Growth Index4.94 (4.65)
Search Engine Demand Index84.99 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (55.23)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other22 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]