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Merck

50843

D-Camphor

analytical standard

Synonym(s):

2-Bornanone, 2-Camphanone

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About This Item

Empirical Formula (Hill Notation):
C10H16O
CAS Number:
464-49-3
Molecular Weight:
152.23
NACRES:
NA.24
PubChem Substance ID:
329757640
UNSPSC Code:
85151701
EC Number:
207-355-2
MDL number:
MFCD00064149

Key Documents

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InChI key

DSSYKIVIOFKYAU-XCBNKYQSSA-N

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

SMILES string

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

Quality Level

100

grade

analytical standard

vapor density

5.24 (vs air)

vapor pressure

4 mmHg ( 70 °C)

assay

≥97.5% (GC)

optical activity

[α]/D +43.0±2.0°, c = 10 in ethanol

autoignition temp.

870 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

3.5 %

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

178-182 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

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General description

D-Camphor is an acyclic terpenoid, that occurs naturally in the wood of Cinnamomum camphora.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Danger

Hazard Classifications

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

target_organs

Lungs

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 1

flash_point_f

147.2 °F - closed cup

flash_point_c

64 °C - closed cup

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

50843-BULK: + 50843-VAR: + 50843-100MG:4548173356709

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2028
BCCH9689
BCCD4182
BCBW7131
BCBQ7460V

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The Pharmacology of Chinese Herbs, Second Edition (1998)
R E White et al.
Archives of biochemistry and biophysics, 228(2), 493-502 (1984-02-01)
Three alicyclic compounds (D-camphor, adamantanone, adamantane) were found to be hydroxylated by the cytochrome P-450 isoenzymes P-450cam and P-450LM2. With P-450cam as the catalyst only one product was formed from each of the substrates: 5-exohydroxycamphor, 5-hydroxyadamantanone, and 1-adamantanol. With P-450LM2
Gustav Georg Belz et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 10 Suppl 4, 61-67 (2003-06-17)
Independent, double-blinded, randomized, placebo-controlled studies using sublingual/oral administration of D-camphor, an extract from fresh crataegus berries, and a combination of the two (CCC) yielded the following results: Both the D-camphor and the extract from fresh crataegus berries, the components of
Jeffrey N Love et al.
The Journal of emergency medicine, 27(1), 49-54 (2004-06-29)
Serious pediatric toxicity resulting from exposure to small amounts of camphor-containing products has long been a problem. Twenty years ago the United States Food and Drug Administration took several actions in an attempt to ameliorate this risk. Despite these changes
J Vilaplana et al.
Actas dermo-sifiliograficas, 98(5), 345-346 (2007-06-09)
We report a case of allergic contact dermatitis due to alcamphor present in a flushing solution used by a 58-year-old woman. It is the first case described in our Division of Allergy and the second one reported in the literature.
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