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59677

Supelco

Methyl dihydrojasmonate, mixture of cis and trans

analytical standard

Synonym(s):

(3-Oxo-2-pentylcyclopentyl)acetic acid methyl ester, Methyl (3-oxo-2-pentylcyclopentyl)acetate

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About This Item

Empirical Formula (Hill Notation):
C13H22O3
CAS Number:
Molecular Weight:
226.31
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

Pricing and availability is not currently available.

grade

analytical standard

Quality Level

Assay

≥96.0% (GC)

shelf life

limited shelf life, expiry date on the label

refractive index

n20/D 1.459 (lit.)

bp

110 °C/0.2 mmHg (lit.)

density

0.998 g/mL at 25 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

SMILES string

CCCCCC1C(CCC1=O)CC(=O)OC

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This Item
C-12901C-14096C-12907
morphology

(mononuclear)

morphology

(mononuclear)

morphology

(mononuclear)

morphology

(mononuclear)

storage temp.

−20°C

storage temp.

−196°C

storage temp.

−20°C

storage temp.

−196°C

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

packaging

pkg of 1,000,000 cells

packaging

pkg of 25,000,000 cells

packaging

pkg of 1,000,000 cells

packaging

pkg of 25,000,000 cells

application(s)

cell analysis (DNA, RNA, and protein)

application(s)

-

application(s)

cell analysis (DNA, RNA, and protein)

application(s)

-

General description

Methyl dihydrojasmonates (MDJ) are grouped under the class of cyclopentanones. MDJ is a widely used fragrance ingredient in perfume industries because of its intense floral, jasmine-like odor. Both the trans and cis methyl dihydrojasmonate mixture may be isolated from Jasminum grandiflorum L.[1][2][3]

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup


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    Evaluation of the developmental toxicity of methyl dihydrojasmonate (MDJ) in rats
    Politano VT, et al.
    International Journal of Toxicology, 27(3), 295-300 (2008)
    Enantioselective synthesis and absolute stereochemistry of both the enantiomers of trans-magnolione, a fragrance structurally related to trans-methyl jasmonate
    Donnoli MI, et al.
    Tetrahedron, 60(23), 4975-4981 (2004)
    Fragrance material review on methyl dihydrojasmonate
    Scognamiglio J, et al.
    Food And Chemical Toxicology, 50(23), S562-S571 (2012)

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