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Key Documents

T3777

Sigma-Aldrich

1-Triacontanol

≥98% (capillary GC)

Synonyme(s) :

1-Hydroxytriacontane, Melissyl alcohol

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About This Item

Formule linéaire :
CH3(CH2)28CH2OH
Numéro CAS:
Poids moléculaire :
438.81
Numéro Beilstein :
1711965
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352104
ID de substance PubChem :
Nomenclature NACRES :
NA.25

Niveau de qualité

Pureté

≥98% (capillary GC)

Forme

powder

Pf

86-87 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

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

Clé InChI

REZQBEBOWJAQKS-UHFFFAOYSA-N

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Catégories apparentées

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).


Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


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Les clients ont également consulté

M K Akitha Devi et al.
Indian journal of experimental biology, 50(10), 729-734 (2012-12-12)
Development of a reproducible, versatile and efficient in vitro plant regeneration system is highly warranted for Indian soybean varieties for their mass multiplication in view of their commercial significance. Accordingly a protocol for direct shoot organogenesis in soybean variety JS
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
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
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

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