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Key Documents

T3777

Sigma-Aldrich

1-Triacontanol

≥98% (capillary GC)

Synonym(s):

1-Hydroxytriacontane, Melissyl alcohol

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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

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

Certificates of Analysis (COA)

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G Sivakumar Swamy et al.
The Journal of membrane biology, 228(3), 165-177 (2009-05-07)
Fluorescence resonance energy transfer (FRET), time-resolved fluorescence and anisotropy decays were determined in large unilamellar vesicles (LUVs) of egg phosphatidylcholine with the FRET pair N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)-1,2-dipalmitoyl-sn-glycero-3-phospho-ethanolamine as donor and lissamine rhodamine B 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine as acceptor, using 2-ps pulses from a Ti:sapphire
Sugey López-Martínez et al.
Natural product research, 27(2), 130-136 (2012-03-01)
Phoradendron brachystachyum is a hemiparasitic plant widely distributed in México that belongs to the Viscaceae family. It has been commonly used in folk medicine as a substitute for the European mistletoe. In this chemical study, morolic acid was isolated as
Shijie Du et al.
Natural product research, 23(14), 1316-1321 (2009-09-08)
A new lactone was isolated from the leaves of Xylocarpus granatum, along with three known compounds: triacontanol, beta-sitosterol and kaempferol-3-O-beta-D-glucoside. Its structure was elucidated as 3-(1-hydroxyethyl)-4,4-dimethyl-4-butyrolactone (1) by infrared, (1)H and (13)C NMR and ESI-MS data. At a concentration of
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
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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