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W379401

(3aR)-(+)-Sclareolide

Name: (3a<I>R</I>)-(+)-Sclareolide
Brand: ALDRICH

natural, 97%, FG

Synonym(s):

Sclareolide

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About This Item

Empirical Formula (Hill Notation):

C₁₆H₂₆O₂

CAS Number:

564-20-5

Molecular Weight:

250.38

FEMA Number:

3794

UNSPSC Code:

12164502

PubChem Substance ID:

329830654

NACRES:

NA.21

EC Number:

209-269-0

Flavis number:

16.055

MDL number:

MFCD00134168

Organoleptic:

woody; paper

Grade:

FG, Fragrance grade, natural

Biological source:

Salvia sclarea L

Agency:

follows IFRA guidelines

Food allergen:

no known allergens

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Properties

biological source

Salvia sclarea L

Quality Level

300, 400

grade

FG, Fragrance grade, natural

agency

follows IFRA guidelines

reg. compliance

EU Regulation 1223/2009, EU Regulation 1334/2008 & 872/2012, FDA 21 CFR 110

assay

97%

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

impurities

may contain ≤0.10% 2-Methylpentane (residual solvent)

mp

124-126 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

sclareol

greener alternative category

Aligned

organoleptic

woody; paper

SMILES string

[H][C@@]12CC[C@@]3(C)OC(=O)C[C@]3([H])[C@@]1(C)CCCC2(C)C

InChI

1S/C16H26O2/c1-14(2)7-5-8-15(3)11(14)6-9-16(4)12(15)10-13(17)18-16/h11-12H,5-10H2,1-4H3/t11-,12+,15-,16+/m0/s1

InChI key

IMKJGXCIJJXALX-SHUKQUCYSA-N

Description

General description

We are committed to bringing you greener alternative products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is Biobased and thus aligns with "Less Hazardous Chemical Syntheses" and "Use of Renewable Feedstocks".

Application

Approach to Merosesquiterpenes via Lewis Acid Catalyzed Nazarov-Type Cyclization.: The synthesis of "(3aR)-(+)-Sclareolide" plays a crucial role in the total synthesis of Akaol A, a merosesquiterpene. This compound is utilized in studies focusing on Lewis acid-catalyzed Nazarov-type cyclization, which is a key reaction for constructing complex cyclic structures within organic molecules. This synthesis process not only expands the capabilities of chemists to build intricate molecular architectures but also enhances the understanding of reaction mechanisms crucial for pharmaceutical development (DOI: 10.1021/acs.orglett.6b00446).

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Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Articles

Fragrance Regulations and Requirements: What You Need to Know

Recent regulatory changes in the US and EU have put the focus on fragrance safety and ingredient transparency, including the MoCRA, to be implemented within the next two years. Manufacturers and suppliers must comply with these changes to ensure they are meeting consumer demand and industry expectations for safety.

Global Trade Item Number

SKU	GTIN
W379401-SAMPLE	04061833654552
W379401-100G	04061833654538
W379401-25G	04061833654545