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334111

Sigma-Aldrich

Dipenten

technical, for use as solvent (for the paint industry), mixture of various terpenes

Synonym(e):

(+/−)-Limonen, p-Mentha-1,8-dien

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About This Item

Empirische Formel (Hill-System):
C10H16
CAS-Nummer:
138-86-3
Molekulargewicht:
136.23
Beilstein:
3587825
EG-Nummer:
205-341-0
MDL-Nummer:
MFCD00062992
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24860056
NACRES:
NA.22

Qualität

for use as solvent (for the paint industry)
technical

Dampfdichte

>4.7 (80 °C, vs air)

Dampfdruck

1 mmHg ( 20 °C)

Form

liquid

Selbstzündungstemp.

458 °F

Zusammensetzung

Major isomer: 3-Carene
Minor isomers: Limonene, β-pinene and α-pinene

Expl.-Gr.

0.7-6.1 %, 150 °F

Brechungsindex

n20/D 1.473 (lit.)

bp

170-180 °C (lit.)

Dichte

0.86 g/mL at 20 °C (lit.)

SMILES String

CC(=C)C1CCC(C)=CC1

InChI

1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3

InChIKey

XMGQYMWWDOXHJM-UHFFFAOYSA-N

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Allgemeine Beschreibung

Dipentene (Limonene) is a monoterpene olefin having potential applications in polymer and fuel chemistry. It is also widely used as flavoring and fragrance agent.[1] Dipentene (limonene) is a promising green solvent.[2] Kinetics of the reactions of limonene with OH and OD radicals has been investigated in a low pressure flow tube reactor coupled with a quadrupole mass spectrometer.[3]

Anwendung

Dipentene was employed as a solvent in the reaction media for enzymatic synthesis of phosphatidylserine.[2]

Sonstige Hinweise

Contains a mixture of terpenes

Signalwort

Warning

Gefahreneinstufungen

Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

109.4 °F - closed cup

Flammpunkt (°C)

43 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCK6104
BCCH8298
BCCC4907
BCBZ6907
BCBW0915

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

17763

(+)-Limonen-1,2-epoxid

Yan-Hong Bi et al.
Biotechnology letters, 37(1), 115-119 (2014-09-13)
The bio-based solvents limonene and p-cymene obtained from citrus waste were innovatively employed as the reaction media for enzymatic synthesis of phosphatidylserine. (R)-(+)-Limonene, which is available in large quantities from citrus waste, and its close derivative p-cymene, are promising green
Tristan Braure et al.
The journal of physical chemistry. A, 118(40), 9482-9490 (2014-09-12)
The kinetics of the reactions of limonene with OH and OD radicals has been studied using a low-pressure flow tube reactor coupled with a quadrupole mass spectrometer: OH + C10H16 → products (1), OD + C10H16 → products (2). The
K Vanommeslaeghe et al.
Journal of chemical information and modeling, 52(12), 3144-3154 (2012-11-14)
Molecular mechanics force fields are widely used in computer-aided drug design for the study of drug-like molecules alone or interacting with biological systems. In simulations involving biological macromolecules, the biological part is typically represented by a specialized biomolecular force field
Keng-Chih Liu et al.
International journal of pharmaceutics, 441(1-2), 687-692 (2012-10-27)
Gap junction protein connexin43 (Cx43) specific antisense oligodeoxynucleotides (AsODN) have been shown to improve a number of inflammatory conditions and may therefore offer a novel strategy for persistent pain management. However, for such molecules to be clinically effective, delivery challenges
Patrizia A d'Alessio et al.
Life sciences, 92(24-26), 1151-1156 (2013-05-15)
To further explore the anti-inflammatory properties of d-Limonene. A rat model was used to compare evolution of TNBS (2,5,6-trinitrobenzene sulfonic acid)-induced colitis after oral feeding with d-Limonene compared to ibuprofen. Peripheral levels of TNF-α (Tumor Necrosis Factor alpha) were assessed
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