ChemicalBook > Product Catalog >Organic Chemistry >Quinones >(1R)-(-)-CAMPHORQUINONE

(1R)-(-)-CAMPHORQUINONE

CAS No.: 10334-26-6

Chemical Name:: (1R)-(-)-CAMPHORQUINONE

Synonyms: 3-Ketocamphor;D-CAMPHORQUINONE;2,3-BORNANEDIONE;D-CAMPHOROQUINONE;D-2,3-BORNANEDIONE;(-)-CAMPHORQUINONE;(-)-2,3-BORNANEDIONE;D-(-)-CAMPHORQUINONE;R-(-)-CAMPHORQUINONE;(1R)-2,3-BORNANEDIONE

CBNumber:: CB6242990

Molecular Formula:: C10H14O2

Molecular Weight:: 166.22

MOL File:: 10334-26-6.mol

MSDS File:: SDS

Modify Date:: 2023/11/2 15:05:42

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(1R)-(-)-CAMPHORQUINONE Properties

Melting point	200-203 °C(lit.)
Boiling point	254.44°C (rough estimate)
alpha	-101° (20/D)(c=2, C6H5CH3)
Density	1.0060 (rough estimate)
refractive index	1.5200 (estimate)
storage temp.	Sealed in dry,Room Temperature
solubility	almost transparency in Methanol
form	powder to crystal
color	Light yellow to Yellow
optical activity	[α]20/D 101°, c = 2 in toluene
BRN	2327696
CAS DataBase Reference	10334-26-6(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)

GHS07,GHS08

Signal word

Danger

Hazard statements

H302-H334

Precautionary statements

P301+P312+P330

Hazard Codes

Risk Statements

22-43

Safety Statements

36/37

WGK Germany

HS Code

2914.29.5000

NFPA 704

	1
0		0

(1R)-(-)-CAMPHORQUINONE price More Price(3)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich(India)	276286	(1R)-(−)-Camphorquinone 99%	10334-26-6	5G	₹15836.98	2022-06-14	Buy
TCI Chemicals (India)	C1482	(1R)-(-)-Camphorquinone min. 98.0 %	10334-26-6	1G	₹3400	2022-05-26	Buy
TCI Chemicals (India)	C1482	(1R)-(-)-Camphorquinone min. 98.0 %	10334-26-6	5G	₹9600	2022-05-26	Buy

Product number	Packaging	Price	Buy
276286	5G	₹15836.98	Buy
C1482	1G	₹3400	Buy
C1482	5G	₹9600	Buy

(1R)-(-)-CAMPHORQUINONE Chemical Properties,Uses,Production

Uses

(1R)-(-)Camphorquinone are used as visible light photoinitiator for biomedical applications such as in dental surgery.

General Description

Camphorquinone, a 1,2-diketone, is a photoinitiator that finds wide use in the curing of resin composites. It functions by initiating the chain polymerization by free radical generation; typically with the aid of co-initiator amines.

Purification Methods

It can be purified by steam distillation, recrystallisation (yellow prisms) from EtOH, *C6H6 or Et2O/pet ether and it can be sublimed in a vacuum. The (±)-quinone forms needles from EtOH, m 197-198o, 203o. [Buxtorf & Flatt Helv Chim Acta 13 1026 1930, Asahena et al. Chem Ber 67 1432 1934, Beiltein 7 I 325.]

(1R)-(-)-CAMPHORQUINONE Preparation Products And Raw materials

Raw materials

Preparation Products

3-Hydroxy-2-bornanone

(1R)-(-)-CAMPHORQUINONE Suppliers

Global( 105)Suppliers

Supplier	Tel	Country	ProdList	Advantage	Inquiry
Opulant Pharmaceuticals Pvt Ltd	+91-8105130349 +91-8105130349	Telangana, India	66	58	Inquiry
S. Nihar Exports	91 22 208 5632	New Delhi, India	232	50	Inquiry
OCEAN TRADING CORPORATION	+91(22) 24921669	New Delhi, India	6211	58	Inquiry
CHEMSWORTH	+91-261-2397244	New Delhi, India	6707	30	Inquiry
TCI Chemicals (India) Pvt. Ltd.	1800 425 7889	New Delhi, India	6778	58	Inquiry
Clearsynth Labs	91-22-45045900	Maharashtra, India	3889	58	Inquiry
Hebei Mojin Biotechnology Co., Ltd	+8613288715578	China	12455	58	Inquiry
Hebei Yanxi Chemical Co., Ltd.	+86-17531190177; +8617531190177	China	5873	58	Inquiry
career henan chemical co	+86-0371-86658258 +8613203830695	China	29826	58	Inquiry
Dideu Industries Group Limited	+86-29-89586680 +86-15129568250	China	24639	58	Inquiry

Supplier	Advantage
Opulant Pharmaceuticals Pvt Ltd	58
S. Nihar Exports	50
OCEAN TRADING CORPORATION	58
CHEMSWORTH	30
TCI Chemicals (India) Pvt. Ltd.	58
Clearsynth Labs	58
Hebei Mojin Biotechnology Co., Ltd	58
Hebei Yanxi Chemical Co., Ltd.	58
career henan chemical co	58
Dideu Industries Group Limited	58

(1R)-(-)-CAMPHORQUINONE Spectrum

(1R)-(-)-CAMPHORQUINONE(10334-26-6)MS (1R)-(-)-CAMPHORQUINONE(10334-26-6)¹HNMR (1R)-(-)-CAMPHORQUINONE(10334-26-6)¹³CNMR (1R)-(-)-CAMPHORQUINONE(10334-26-6)IR1 (1R)-(-)-CAMPHORQUINONE(10334-26-6)IR2 (1R)-(-)-CAMPHORQUINONE(10334-26-6)Raman

10334-26-6((1R)-(-)-CAMPHORQUINONE)Related Search:

L-CAMPHORQUINONE,L-(+)-CAMPHORQUINONE,S-(+)-CAMPHORQUINONE,CAMPHORQUINONE, -S-(+)-,(1S)-(+)-CAMPHORQUINONE,(+)-CAMPHORQUINONE (1R)-(-)-CAMPHORQUINONE DL-CAMPHORQUINONE (1S,E)-(-)-CAMPHORQUINONE 3-OXIME (+/-)-CAMPHORQUINONE,CAMPHORQUINONE,RAC-CAMPHORQUINONE,DL-CAMPHORQUINONE

DL-Camphor Camphor Camphorquinone-10-sulfonyl Chloride ANTI-(1S)-(-)-CAMPHORQUINONE 3-OXIME 9&,ANTI-(1S)-(-)-CAMPHORQUINONE 3-OXIME, 99 % ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME

CAMPHORQUINONE-1-SULPHONYLNORLEUCINE,CAMPHORQUINONE-10-SULFONYLNORLEUCINE CAMPHORQUINONE-10-SULFONIC ACID, HYDRATE,CAMPHORQUINONE-1-SULFONIC ACID, HYDRATE,Camphorquinone-10-sulfonic Acid, Hydrate Technical Grade ANTI-(1R)-(+)-CAMPHORQUINONE 3-OXIME,(1R,E)-(+)-CAMPHORQUINONE 3-OXIME,camphorquinone 3-oxime CAMPHORQUINONE, -R-(-)-(RG) CAMPHORQUINONE, -S-(+)-(RG)

Camphorquinone-10-sulphonic acid hydrate DL-CAMPHORQUINONE, (2,3-BORNANEDIONE) ANTI-(1S)-(-)-CAMPHORQUINONE 3-OXIME,(-)-CAMPHORQUINONE-3-MONOXIME

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CAMPHORQUINONE, -R-(-)- (-)-CAMPHORQUINONE D-2,3-BORNANEDIONE D-CAMPHOROQUINONE D-(-)-CAMPHORQUINONE D-CAMPHORQUINONE (-)-2,3-BORNANEDIONE 2,3-BORNANEDIONE (1R)-(-)-CAMPHORQUINONE (1R)-(-)-2,3-BORNANEDIONE (1R)-2,3-BORNANEDIONE D-(-)-Camphorquinone,98% Bicyclo2.2.1heptane-2,3-dione, 1,7,7-trimethyl-, (1R,4S)- R-(-)-CAMPHORQUINONE 3-Ketocamphor (1R)-(-)-2,3-Bornanedione, 2,3-Bornanedione (1R)-(-)-2,3-camphanedione (1R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (1R,4S)-1β,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (1R,4α)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione (1R)-(-)-CAMPHORQUINONE FOR SYNTHESIS (1R)-1,7,7-triMethylbicyclo[2.2.1]heptane-2,3-dione (1R)-(-)-Camphorquinone 99% (1R)-(-)-Camphorquinone (1R)-bornane-2,3-dione (1R)-(-)-Camphorquinone> (1R)-(-)-CAMPHORQUINONE ISO 9001：2015 REACH (1S,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione 10334-26-6 Asymmetric Synthesis Ketones Organic Building Blocks Chiral Building Blocks Bicyclic Monoterpenes Terpenes Anthraquinones, Hydroquinones and Quinones Bicyclic Monoterpenes Biochemistry Terpenes