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O5500

Sigma-Aldrich

Octyl acetate

≥99%

Sinónimos:

Acetic acid octyl ester

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About This Item

Fórmula lineal:
CH3CO2(CH2)7CH3
Número de CAS:
112-14-1
Peso molecular:
172.26
EC Number:
203-939-6
MDL number:
MFCD00009562
UNSPSC Code:
12352100
PubChem Substance ID:
24898017
NACRES:
NA.22

vapor density

5.9 (vs air)

assay

≥99%

autoignition temp.

515 °F

expl. lim.

8.14 %

refractive index

n20/D 1.418 (lit.)

bp

211 °C (lit.)

density

0.867 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCOC(C)=O

InChI

1S/C10H20O2/c1-3-4-5-6-7-8-9-12-10(2)11/h3-9H2,1-2H3

InChI key

YLYBTZIQSIBWLI-UHFFFAOYSA-N

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Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

189.1 °F - closed cup

flash_point_c

87.3 °C - closed cup

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P J A de Bruijn et al.
Journal of evolutionary biology, 29(3), 665-671 (2015-12-22)
Animals often respond to danger by raising alarm to inform others. Alarm signals come in many different forms, such as visual or mechanical display, sound or odour. Some animals produce vocal alarm signals that vary with the level of danger.
Anett Kirschner et al.
Applied microbiology and biotechnology, 73(5), 1065-1072 (2006-09-01)
A gene encoding a Baeyer-Villiger monooxygenase (BVMO) identified in Pseudomonas fluorescens DSM 50106 was cloned and functionally expressed in Escherichia coli JM109. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blot analysis showed an estimated 56 kDa-size protein band corresponding
Pachara Sattayawat et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(3), 1404-1413 (2020-01-10)
Bio-based production technologies may complement or replace petroleum-based production of chemicals, but they face a number of technical challenges, including product toxicity and/or water insolubility. Plants and microorganisms naturally biosynthesize chemicals that often are converted into derivatives with reduced toxicity
Seyed Mehdi Razavi et al.
Natural product research, 24(12), 1125-1130 (2009-07-17)
The chemical composition of essential oil obtained by hydrodistillation from the dried fruits of Zosima absinthifolia was analysed by GC-MS. Twenty-four compounds were characterised in the oil. The major components of the oil were octyl acetate (87.48%), octyl octanoate (5.03%)
W C Daughtrey et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 12(2), 313-320 (1989-02-01)
The subchronic toxicity of octyl acetate was assessed following its administration to rats via oral gavage, 5 days per week for 13 weeks. Treated rats received undiluted octyl acetate at doses of 0.1, 0.5, or 1.0 g/kg. Control rats received
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