T3777
1-Triacontanol
≥98% (capillary GC)
Synonym(s):
1-Hydroxytriacontane, Melissyl alcohol
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All Photos(3)
About This Item
Linear Formula:
CH3(CH2)28CH2OH
CAS Number:
Molecular Weight:
438.81
Beilstein:
1711965
EC Number:
MDL number:
UNSPSC Code:
12352104
PubChem Substance ID:
NACRES:
NA.25
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Quality Level
Assay
≥98% (capillary GC)
form
powder
mp
86-87 °C (lit.)
storage temp.
2-8°C
SMILES string
CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
InChI
1S/C30H62O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h31H,2-30H2,1H3
InChI key
REZQBEBOWJAQKS-UHFFFAOYSA-N
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Application
- The Relationships between Waxes and Storage Quality Indexes of Fruits of Three Plum Cultivars.: This study examines how 1-Triacontanol affects the storage and quality of plums. By analyzing waxes that include 1-Triacontanol, the research helps understand its impact on extending the shelf life of fruits, which is crucial for agricultural economics and food sustainability (Zhu et al., 2023).
- Mitigation of salt stress in Indian mustard (Brassica juncea L.) by the application of triacontanol and hydrogen sulfide.: This research explores the use of 1-Triacontanol to alleviate salt stress in Indian mustard plants, offering insights into how it enhances plant growth under stress conditions. Such studies are vital for improving crop resilience to environmental stresses, thus contributing to sustainable agriculture practices (Verma et al., 2023).
- The Effect of the Stress-Signalling Mediator Triacontanol on Biochemical and Physiological Modifications in Dracocephalum forrestii Culture.: The study delves into how 1-Triacontanol acts as a stress mediator in plant cultures, highlighting its potential to induce biochemical and physiological changes that could lead to enhanced secondary metabolite production in medicinal plants (Weremczuk-Jezyna et al., 2022).
- Triacontanol priming as a smart strategy to attenuate lead toxicity in Brassica oleracea L.: This investigation shows the effectiveness of 1-Triacontanol in mitigating lead toxicity in plants, providing a strategy to protect crops from heavy metal contamination, thereby ensuring food safety and environmental health (Ahmed et al., 2023).
Storage Class Code
11 - Combustible Solids
WGK
nwg
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Krishnamurthy Ramanarayan et al.
Journal of plant physiology, 161(4), 489-492 (2004-05-07)
Triacontanol (TRIA), a long chain aliphatic alcohol (C30H61OH) reverses the effect of jasmonic acid (JA) in inducing proteinase inhibitors (PIs) in tomato leaves. Porcine pancreas trypsin and Spodoptera litura gut proteinases were inhibited in the presence of leaf proteins treated
Z Zhang et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 22(1), 28-29 (2003-02-11)
From the ethanol extract of Lysimachia pentapetala, six compounds have been isolated. These compounds were identified as triacontanol, beta-sitosterol, glycerol monopalmitate, succinic acid, flavonol glycosides and hitrite upon the date of mp, IR, MS and 1HNMR tests.
Neena Srivastava et al.
Journal of chromatographic science, 47(10), 936-939 (2009-11-26)
A high-performance thin layer chromatographic method has been established for the identification and standardization of Stereospermum suaveolens extracts using two active biomarkers viz. triacontanol and p-coumaric acid in root samples collected from different geographical locations of India. These marker components
Xiao-Dong Jia et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 31(7), 988-990 (2008-11-01)
To study the chemical constituents of flower buds of Lonicera macranthoides. The 90% EtOH extract of Lonicera macranthoides. was successively partitioned with petroleum ether and ethyl acetete. Repeated column chromatography of the ethyl acetete fraction afforded the following compounds (1-9):
Muhammad Arif Lodhi et al.
Natural product research, 21(8), 721-725 (2007-07-10)
The mechanism of inhibition of jack bean and Bacillus pasteurii ureases was investigated by triacontanyl palmitate (1) which is a long-chain fatty ester and has been isolated from Symplocos racemosa Roxb. Lineweaver-Burk, Dixon plots, and their secondary replots showed that
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