(+)-Camphor

Name: (+)-Camphor
Brand: BOC Sciences
Rating: 5 (1 reviews)

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Molecular Formula:

C10H16O

Molecular Weight:

152.23

CAS Number:

464-49-3

Catalog Number:

464-49-3

Product Information

Molecular Formula:

C10H16O

Molecular Weight:

152.23

Description

(+)-Camphor is a terpenoid used as a culinary flavoring agent in parts of Asia. It has insecticidal activity and is also used as an antimicrobial agent.

Synonyms

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R,4R)-; Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)-; Camphor, (1R,4R)-(+)-; (+)-(1R,4R)-Camphor; (+)-2-Bornanone; (1R)-(+)-Camphor; (1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one; (1R)-Camphor; (1R,4R)-(+)-Camphor; (R)-(+)-Camphor; (R)-Camphor; D-(+)-Camphor; D-Camphor; Alcanfor; Camphor, (+)-; d-Camphor; Dextrocamphora; Japanese camphor

IUPAC Name

(1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

Canonical SMILES

CC1(C2CCC1(C(=O)C2)C)C

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

Boiling Point

207.4°C

Melting Point

178.8°C

Flash Point

64°C

Purity

≥98%

Density

0.982±0.06 g/cm3

Solubility

Soluble in Chloroform (Slightly), Ethanol (Slightly), Methanol (Slightly)

Appearance

White Sticky Solid

Shelf Life

As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly

Storage

Store at -20°C

Stability

Stable. Incompatible with strong reducing agents, strong oxidizing agents, chlorinated solvents. Protect from direct sunlight.

LogP

2.380

Vapor Pressure

1 mmHg at 106.7 °F

Safety Information

Hazards

H228:
Flammable solid.
H302:
Harmful if swallowed.
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.

Precautionary Statement

P210:
Keep away from heat, sparks, open flames, hot surfaces. No smoking.
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P370+P378:
In case of fire:
Use for extinction:
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.

Computed Properties

XLogP3

2.2

Hydrogen Bond Donor Count

Hydrogen Bond Acceptor Count

Rotatable Bond Count

Exact Mass

152.120115130 g/mol

Monoisotopic Mass

152.120115130 g/mol

Topological Polar Surface Area

17.1Å²

Heavy Atom Count

Formal Charge

Complexity

217

Isotope Atom Count

Defined Atom Stereocenter Count

Undefined Atom Stereocenter Count

Defined Bond Stereocenter Count

Undefined Bond Stereocenter Count

Covalently-Bonded Unit Count

Compound Is Canonicalized

Yes

Patents

Publication Number	Title	Priority Date
CN-113648387-A	Plant extract for repairing beta islet cells and reducing blood glucose, and preparation method and application thereof	2021-08-20
CN-113318121-A	Medicine for treating diabetic retinopathy and preparation method thereof	2021-06-23
CN-113018355-A	Auxiliary external application medicine for thoracic cavity tumor and abdominal cavity tumor and using method thereof	2021-03-16
RU-2750161-C1	Method for producing d-camphor anils	2020-12-11
CN-213886317-U	Camphor powder stoving reducing mechanism	2020-12-08
CN-112358757-A	Strippable protective film coating and preparation method and application thereof	2020-10-26
US-10912753-B1	Topical skin care composition	2020-10-20
CN-112618676-A	Application of gynura segetum and extract thereof in preparing medicine for treating and/or preventing vascular endothelial injury	2020-10-10
US-11033516-B1	Combination therapies with disulfiram	2020-09-18
WO-2022054917-A1	Mouth-coating feel enhancer	2020-09-11

Literatures

PMID	Publication Date	Title	Journal
31702924	2020-01-09	Discovery of Nonpungent Transient Receptor Potential Vanilloid 1 (TRPV1) Agonist as Strong Topical Analgesic	Journal of medicinal chemistry
22461383	2012-08-01	Quantitative structure-activity relationships of monoterpenoid binding activities to the housefly GABA receptor	Pest management science
21162008	2010-12-01	Chemical variations of the essential oils in flower heads of Chrysanthemum indicum L. from China	Chemistry & biodiversity
20565070	2010-07-23	An efficient and economical MTT assay for determining the antioxidant activity of plant natural product extracts and pure compounds	Journal of natural products
20356305	2010-07-22	Transient receptor potential ankyrin 1 (TRPA1) channel as emerging target for novel analgesics and anti-inflammatory agents	Journal of medicinal chemistry
17684094	2007-08-14	4-Hydroxynonenal, an endogenous aldehyde, causes pain and neurogenic inflammation through activation of the irritant receptor TRPA1	Proceedings of the National Academy of Sciences of the United States of America
16939314	2006-09-06	Chemical composition and antifungal activity of Salvia macrochlamys and Salvia recognita essential oils	Journal of agricultural and food chemistry
15646539	2004-08-01	[Drug-induced liver injury; fourteenth updated edition of the bibliographic database of liver injuries and related drugs]	Gastroenterologie clinique et biologique
15161226	2004-06-02	chemical composition, plant genetic differences, antimicrobial and antifungal activity investigation of the essential oil of Rosmarinus officinalis L	Journal of agricultural and food chemistry
12444669	2002-11-01	Screening of ubiquitous plant constituents for COX-2 inhibition with a scintillation proximity based assay	Journal of natural products