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W223018

Sigma-Aldrich

D-Camphor

≥97%, FG

Synonym(s):

2-Bornanone, 2-Camphanone

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
Molecular Weight:
152.23
FEMA Number:
2230
EC Number:
Council of Europe no.:
140
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
7.215
NACRES:
NA.21

biological source

synthetic

Quality Level

grade

FG
Halal
Kosher

agency

meets purity specifications of JECFA

reg. compliance

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515

vapor density

5.24 (vs air)

vapor pressure

4 mmHg ( 70 °C)

assay

≥97%

form

crystals

optical activity

[α]25/D +44°, c = 10 in ethanol

autoignition temp.

870 °F

expl. lim.

3.5 %

mp

178-182 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

camphoraceous; woody; minty; herbaceous; phenolic; warm

SMILES string

CC1(C)[C@@H]2CC[C@@]1(C)C(=O)C2

InChI

1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3/t7-,10+/m1/s1

InChI key

DSSYKIVIOFKYAU-XCBNKYQSSA-N

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Related Categories

General description

D-Camphor is a volatile terpenoid that can be used as a flavoring agent and a fragrance ingredient. It has been identified as the major volatile component in the essential oil extracted from the leaves of Blumea balsamifera and Ashe juniper.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 2 Inhalation

target_organs

Lungs

wgk_germany

WGK 1

flash_point_f

closed cup

flash_point_c

closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Camphor (dl) primary reference standard

02070595

Camphor (dl)

(−)-Borneol predominantly endo, 97%

Sigma-Aldrich

139114

(−)-Borneol

(+)-Borneol analytical standard

Supelco

68878

(+)-Borneol

Gas-liquid chromatography of terpenes. Part XVI. The volatile oil of the leaves of Juniperus ashei Buchholz
Rudloff EV
Canadian Journal of Chemistry, 46(5), 679-683 (1968)
Yannai S
Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients, 221-221 (2012)
Chemical components in volatile oil from Blumea balsamifera (L.) DC
Bhuiyan MNI, et al.
Bangladesh Journal of Botany, 38(1), 107-109 (2009)
Christian Merten et al.
The journal of physical chemistry. A, 116(27), 7329-7336 (2012-06-06)
In the present work, the first observation of strong resonance Raman optical activity (RROA) involving more that one resonant electronic state is reported. The chiral transition metal complex bis-(trifluoroacetylcamphorato) copper(II), abbreviated Cu(tfc)(2), exhibits both resonance Raman (RR) and RROA spectra
Hiroyuki Kitahata et al.
Physical review. E, Statistical, nonlinear, and soft matter physics, 87(1), 010901-010901 (2013-02-16)
The coupling between deformation and motion in a self-propelled system has attracted broader interest. In the present study, we consider an elliptic camphor particle for investigating the effect of particle shape on spontaneous motion. It is concluded that the symmetric

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