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Merck
CN

237809

1-Triacontanol

96%

Synonym(s):

1-Hydroxytriacontane, Melissyl alcohol

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About This Item

Linear Formula:
CH3(CH2)28CH2OH
CAS Number:
Molecular Weight:
438.81
EC Number:
209-794-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1711965
MDL number:
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assay

96%

mp

86-87 °C (lit.)

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



Storage Class

11 - Combustible Solids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Burcu Ertit Taştan et al.
Journal of hazardous materials, 246-247, 173-180 (2013-01-10)
The effect of engine exhaust emissions on air pollution is one of the greatest problems that the world is facing today. The study focused on the effects of realistic levels of engine exhaust emissions of liquid petroleum gas (LPG) and
Ravindra B Malabadi et al.
Journal of plant physiology, 162(4), 473-478 (2005-05-20)
Successful shoot regeneration of Dendrobium nobile was achieved using thin shoot tip sections and triacontanol (TRIA) for the first time. Protocorm-like bodies (PLBs) or proliferating shoot buds were observed when thin shoot tip sections were cultured on the basal medium
Xian-Yin Lai et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 31(19), 1597-1600 (2006-12-15)
To study the chemical constituents of Abelmoschus manihot. Chromatographic methods were used to isolate compounds from A. manihot, and spectroscopic methods were used to identify the structures. Thirteen compounds, myricetin (1), cannabiscitrin (2), myricetin-3-O-beta-D-glucopyranoside (3), glycerolmonopalmitate (4), 2, 4-dihydroxy benzoic