camphor

76-22-2

2-Camphanone

DL-Camphor

2-Bornanone

(+/-)-Camphor

1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

Bornan-2-one

(+)-Camphor

Alphanon

Kampfer

21368-68-3

Formosa camphor

Laurel camphor

Matricaria camphor

Camphor, synthetic

Bornane, 2-oxo-

1,7,7-Trimethylnorcamphor

464-48-2

Japan camphor

2-Camphonone

Huile de camphre

2-Kamfanon

l-(-)-Camphor

2-Keto-1,7,7-trimethylnorcamphane

1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone

D-(+)-Camphor

Norcamphor, 1,7,7-trimethyl-

DTXSID5030955

CHEBI:36773

4,7,7-trimethylbicyclo[2.2.1]heptan-3-one

DL-Bornan-2-one

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-

Caswell No. 155

SYNTHETIC CAMPHOR

DTXCID3010955

1,7,7-Trimethylbicyclo(2.2.1)-2-heptanone

1,7,7-Trimethylbicyclo(2.2.1)heptan-2-one

Zang Qi

HSDB 37

(-)-Alcanfor

MFCD00074738

( inverted exclamation markA)-Camphor

Camphor, (1R,4R)-(+)-

Camphor, (+/-)-

EINECS 200-945-0

EINECS 244-350-4

UNII-5TJD82A1ET

EPA Pesticide Chemical Code 015602

BRN 1907611

BRN 3196099

AI3-18783

(1RS,4RS)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-one

Formosa

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (.+/-.)-

Camphor (USP)

EC 200-945-0

0-07-00-00135 (Beilstein Handbook Reference)

4-07-00-00213 (Beilstein Handbook Reference)

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)-

racemic camphor

NSC26351

DisperseYellow3

MFCD00064149

Camphor, natural

DL-2-Bornanone

8008-51-3

()-Camphor

Heet (Salt/Mix)

Sarna (Salt/Mix)

(?)-Camphor

dl-Camphor (JP17)

(.+/-.)-Camphor

SCHEMBL16068

Camphor, (.+/-.)-

MLS001055495

CHEMBL15768

DivK1c_000724

GTPL2422

HMS502E06

KBio1_000724

Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S)-

NINDS_000724

HMS2268A06

HMS3885J06

HY-N0808

Tox21_200237

BBL012963

s3851

s4516

STK803534

AKOS000118728

AKOS022060577

AC-5284

CCG-266237

CCG-266238

DB14156

LMPR0102120001

MCULE-2476865084

UN 2717

CAS-76-22-2

IDI1_000724

USEPA/OPP Pesticide Code: 015602

NCGC00090681-05

NCGC00090730-01

NCGC00090730-02

NCGC00090730-05

NCGC00257791-01

1ST40229

AC-15523

SMR000386909

SY035827

VS-03622

(1R,4R)-1,7,7-trimethylnorbornan-2-one

DB-051377

DB-056037

DB-070734

C1251

CS-0009813

NS00003762

4,7,7-trimethyl-3-bicyclo[2.2.1]heptanone

EN300-19186

1,7,7-trimethyl-bicyclo[2.2.1]heptan-6-one

C00809

C18369

D00098

E75814

1,7,7-Trimethyl-bicyclo[2.2.1]heptan-2-one

A838646

Q181559

Q-200784

W-109539

W-110530

(+/-)-1,7,7-trimethyl-bicyclo[2,2,1]heptane-2-one

F0001-0763

Z104473074

The Henry's Law constant for camphor is estimated as 8.3X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 0.65 mm Hg(1), and water solubility, 1.570X10+3 mg/L(2). This Henry's Law constant indicates that camphor is expected to volatilize from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 17 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 9 days(SRC). Camphor's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Camphor is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Jones AH; J Chem Eng Data 5: 196-200 (1960) (2) Yalkowky SH et al; Handbook of Aqueous Solubility Data. 2nd ed., Boca Raton, FL: CRC Press, p. 721 (2010) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of camphor can be estimated to be 117(SRC). According to a classification scheme(2), this estimated Koc value suggests that camphor is expected to have high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of May 21, 2014: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)