ChemicalBook--->CAS DataBase List--->21368-68-3

21368-68-3

21368-68-3 Structure

21368-68-3 Structure
IdentificationMore
[Name]

DL-Camphor
[CAS]

21368-68-3
[Synonyms]

1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-ONE
1,7,7-TRIMETHYLNORBORNAN-2-ONE
BORNAN-2-ONE
(+/-)-CAMPHOR
CAMPHOR
CAMPHOR, DL-
CAMPHOR GUM
CAMPHOR SYNTHETIC
DL-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTA-2-ONE
DL-2-CAMPHANONE
DL-2-KETO-1,7,7-TRIMETHYLNORCAMPHANE
DL-CAMPHOR
DL-Camphor-synthetic
FORMOSA CAMPHOR
GUM CAMPHOR
JAPAN CAMPHOR
LAUREL CAMPHOR
MATRICARIA CAMPHOR
SYNTHETIC CAMPHOR
7,7-trimethyl-(+-)-bicyclo(2.2.1)heptan-2-on
[EINECS(EC#)]

200-945-0
[Molecular Formula]

C10H16O
[MDL Number]

MFCD00074738
[Molecular Weight]

152.23
[MOL File]

21368-68-3.mol
Chemical PropertiesBack Directory
[Melting point ]

175-177 °C(lit.)
[alpha ]

-1~+1°(20℃/D)(c=10,C2H5OH)
[Boiling point ]

204 °C(lit.)
[density ]

0.992
[vapor density ]

5.2 (vs air)
[vapor pressure ]

4 mm Hg ( 70 °C)
[FEMA ]

4513 | dl-CAMPHOR
[refractive index ]

1.5462 (estimate)
[Fp ]

148 °F
[JECFA Number]

2199
[LogP]

2.13
[CAS DataBase Reference]

21368-68-3(CAS DataBase Reference)
[NIST Chemistry Reference]

Camphor(DL)(21368-68-3)
[EPA Substance Registry System]

21368-68-3(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
[Signal word ]

Warning
[Hazard statements ]

H228-H319-H335-H302-H315
[Precautionary statements ]

P210-P240-P241-P280-P370+P378-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P-P264-P270-P301+P312-P330-P501
[Hazard Codes ]

F,Xn
[Risk Statements ]

R11:Highly Flammable.
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
R36:Irritating to the eyes.
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
[Safety Statements ]

S16:Keep away from sources of ignition-No smoking .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[RIDADR ]

UN 2717 4.1/PG 3
[WGK Germany ]

1
[RTECS ]

EX1225000
[REACH Registrations]

Active
[HazardClass ]

4.1
[PackingGroup ]

III
[HS Code ]

29142910
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

(+/-)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one(21368-68-3).msds
Questions And AnswerBack Directory
[Application]

This product is a white crystalline powder or a colorless, translucent hard lump with a pungent, characteristic odor and an initially pungent taste followed by a cooling sensation. It is easily volatile at room temperature and readily soluble in ethanol, fatty oils, or volatile oils, but only slightly soluble in water. Camphor has a weak antiseptic effect. When applied to the skin, it stimulates the skin's cold receptors, producing a cooling sensation, thus inhibiting itching and providing an antipruritic effect. Vigorous rubbing reflexively causes vasodilation and skin redness. Camphor also has some weak local anesthetic effects. This product can be formulated into camphor liniment, which is taken internally as a stimulant and carminative, and externally as a skin irritant for neuralgia, muscle pain, or joint pain. Its local irritant effect can also be used to treat frostbite (unbroken lesions). This product, combined with menthol and other ingredients, forms compound camphor ointment, which has antipruritic, antiseptic, and local blood circulation-improving effects, and is used for unbroken frostbite, neurodermatitis, etc. It can also be mixed with peanut oil to make a 20% camphor liniment, which is a mild irritant and is often used for neuralgia, muscle pain or joint pain.
Hazard InformationBack Directory
[Chemical Properties]

A white crystalline powder or a colorless translucent lump, with a pungent odor, acrid at first, cool afterward, volatile at room temperature, easily soluble in ethanol, fatty oil or volatile oil, and very slightly soluble in water . Camphor has a weak antiseptic effect.
[Definition]

ChEBI: Camphor is a cyclic monoterpene ketone that is bornane bearing an oxo substituent at position 2. A naturally occurring monoterpenoid. It has a role as a plant metabolite. It is a bornane monoterpenoid and a cyclic monoterpene ketone.
[Synthesis]

DL-Camphor is prepared by reacting borneol With cyclopentadiene catalysted by palladium and rhodium.
Spectrum DetailBack Directory
[Spectrum Detail]

DL-Camphor(21368-68-3)MS
DL-Camphor(21368-68-3)1HNMR
DL-Camphor(21368-68-3)IR1
DL-Camphor(21368-68-3)IR2
DL-Camphor(21368-68-3)Raman
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