Home Categories Chemical Reagents D(+)-Camphor
A6948958

D(+)-Camphor , 10mMinDMSO , 464-49-3

Synonym(s):
(+)-Camphor;(1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one;2-Bornanone;2-Camphanone

CAS NO.:464-49-3

Empirical Formula: C10H16O

Molecular Weight: 152.23

MDL number: MFCD00064149

EINECS: 207-355-2

Pack Size Price Stock Quantity
1ml RMB159.20 In Stock
others     Enquire
Update time: 2022-07-08

PRODUCT Properties

Melting point: 178-182 °C (lit.)
alpha  D25 +41 to +43° (c = 10 in U.S.P. alcohol) according to U.S.P. specif
Boiling point: 204 °C
Density  0,99 g/cm3
vapor density  5.24 (vs air)
vapor pressure  4 mm Hg ( 70 °C)
FEMA  2230 | D-CAMPHOR
refractive index  44.5 ° (C=20, EtOH)
Flash point: 148 °F
storage temp.  2-8°C
solubility  Slightly soluble in water, very soluble in alcohol and in light petroleum, freely soluble in fatty oils, very slightly soluble in glycerol.
form  Crystals
color  White
Odor at 10.00 % in dipropylene glycol. camphor minty phenolic herbal woody
Odor Type camphoreous
explosive limit 3.5%
optical activity [α]25/D +44°, c = 10 in ethanol
Water Solubility  Soluble in water (0.1 g/L at 20°C).
Merck  14,1732
JECFA Number 1395
BRN  2042745
Stability: Stable. Incompatible with strong reducing agents, strong oxidizing agents, chlorinated solvents. Protect from direct sunlight.
LogP 2.3 at 20℃

Description and Uses

(1R)-(+)-Camphor is a terpene that has been found in C. sativa, C. indica, and C. sativa/C. indica hybrid strains as well as the essential oils from a variety of herbs including rosemary, lavender, and sage and has diverse biological activities. It inhibits norepinephrine secretion and cytosolic calcium and sodium increases induced by the nicotinic acetylcholine receptor (nAChR) agonist 1,1-dimethyl-4-phenylpiperazinium iodide (DMPP) in chromaffin cells (IC50s = 70, 88, and 19 μM, respectively). (1R)-(+)-Camphor (65-260 μM) induces proliferation of and increases expression of collagen IA, collagen IIIA, collagen IVA, and elastin in human primary dermal fibroblasts. In vivo, (1R)-(+)-camphor increases expression of collagen IA, collagen IIIA, collagen IVA, and elastin in skin in UV-exposed mice when administered at doses of 26 and 55 mM in drinking water post UV-exposure. It reduces cough frequency in citric acid-challenged guinea pigs. (1R)-(+)-Camphor is insecticidal, reducing digging activity and inducing mortality of fire ant workers. It has also been used as a building block in the synthesis of cannabinergic ligands.

D-Camphor may be used as reference material for the quantification of the analyte in Saraca asoca and coriander using chromatography techniques.

Safety

Symbol(GHS) 
GHS02,GHS05,GHS07,GHS08
Signal word  Danger
Hazard statements  H228-H315-H318-H332-H371
Precautionary statements  P210-P280-P302+P352-P304+P340+P312-P305+P351+P338-P308+P311
Hazard Codes  F,Xn,Xi
Risk Statements  11-22-36/37/38-20/21/22-36
Safety Statements  16-26-36-37/39
RIDADR  UN 2717 4.1/PG 3
WGK Germany  1
RTECS  EX1260000
Autoignition Temperature 870 °F
TSCA  Yes
HazardClass  4.1
PackingGroup  III
HS Code  29142910

RELATED PRODUCTS