Camphor - CAS 76-22-2

Catalog:	BB035523
Product Name:	Camphor
CAS:	76-22-2
Synonyms:	Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-; (±)-Camphor; 1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone; 1,7,7-Trimethylnorcamphor; 2-Bornanone; 2-Camphanone; DL-Camphor; Alphanon; Borneo camphor; dl-Camphor; HCXL 8899; MeSH ID: D002164; Racemic camphor; Root bark oil; Spirit of camphor
Application:	Anti-infective agents, Local

Technical Data

Related CAS:	8013-55-6 (Deleted CAS) 8022-77-3 (Deleted CAS) 21368-68-3 (Deleted CAS) 48113-22-0 (Deleted CAS)
IUPAC Name:	1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
Description:	Camphor is found in the wood of the camphor laurel (Cinnamomum camphora), a large evergreen tree found in East Asia. It can be used as a repellent, a plasticizer for nitrocellulose, a moth repellent, and an antimicrobial substance.
Molecular Weight:	152.23
Molecular Formula:	C10H16O
Canonical SMILES:	CC1(C2CCC1(C(=O)C2)C)C
InChI:	InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3
InChI Key:	DSSYKIVIOFKYAU-UHFFFAOYSA-N
Boiling Point:	204°C
Melting Point:	179°C
Flash Point:	150 °F
Purity:	≥95%
Density:	0.992 g/cm³
Solubility:	Soluble in Acetone (Slightly), Chloroform (Slightly), Ethyl Acetate (Slightly)
Appearance:	White to Pale Yellow Solid
Storage:	Store at -20°C
MDL:	MFCD00064148
LogP:	2.40170
Quality Standard:	Enterprise Standard
Refractive Index:	1.5462 at 20 °C/D
Stability:	Stable. Combustible. Incompatible with strong oxidizing agents, metallic salts, combustible materials, organics.
Vapor Pressure:	4 mm Hg ( 70 °C)

GHS Hazard Statement:	H228 (99.77%): Flammable solid [Danger Flammable solids]
Precautionary Statement:	P210, P240, P241, P260, P261, P264, P270, P271, P280, P301+P312, P304+P312, P304+P340, P309+P311, P312, P330, P370+P378, P405, and P501
Signal Word:	Warning

Publication Number	Title	Priority Date
US-10912753-B1	Topical skin care composition	20201020
US-11033516-B1	Combination therapies with disulfiram	20200918
US-PP32523-P2	Caladium plant named â€˜MOL 158-47â€™	20200423
US-PP32561-P2	Caladium plant named â€˜CRM OF14-219â€™	20200423
US-10993958-B1	Aldehyde functional monoterpenoids for the treatment of coronavirus infection	20200316

PMID	Publication Date	Title	Journal
30597193	20190301	4-Methylbenzylidene-camphor inhibits proliferation and induces reactive oxygen species-mediated apoptosis of human trophoblast cells	Reproductive toxicology (Elmsford, N.Y.)
30496739	20190201	Oleanolic acid promotes orofacial antinociception in adult zebrafish (Danio rerio) through TRPV1 receptors	Chemico-biological interactions
29723517	20180601	Inhibitory effect of α-terpinyl acetate on cytochrome P450 2B6 enzymatic activity	Chemico-biological interactions
29655911	20180501	Antinociceptive activity of Riparin II from Aniba riparia: Further elucidation of the possible mechanisms	Chemico-biological interactions
29445768	20180101	HsTRPA of the Red Imported Fire Ant, Solenopsis invicta, Functions as a Nocisensor and Uncovers the Evolutionary Plasticity of HsTRPA Channels	eNeuro

Complexity:	217
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	152.120115130
Formal Charge:	0
Heavy Atom Count:	11
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	152.120115130
Rotatable Bond Count:	0
Topological Polar Surface Area:	17.1 Å²
Undefined Atom Stereocenter Count:	2
Undefined Bond Stereocenter Count:	0
XLogP3:	2.2