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(±)-Camphor - 96%, high purity , CAS No.76-22-2, Gating inhibitor of TRPA1;Activator of TRPV1;Activator of TRPV3

Moligand™
≥96%

CAS#: 76-22-2
Formula: C₁₀H₁₆O
Molecular Weight: 152.23
Beilstein Registry Number: 1907611
EC Number: 200-945-0
MDL number: MFCD00074738
PubChem CID: 2537

Item Number

C110690

Grouped product items
SKU	Size	Availability	Price	Qty
C110690-100g	100g	In stock	$24.90
C110690-500g	500g	In stock	$33.90

View related series

TRPA1 Gating inhibitor TRPV1 Activator TRPV3 Activator

Basic Description

Synonyms	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\|21368-68-3\|Alphanon\|Kampfer\|Formosa camphor\|Laurel camphor\|Matricaria camphor\|Camphor, synthetic\|Bornane, 2-oxo-\|464-48-2\|
Specifications & Purity	Moligand™, ≥96%
Shipped In	Normal
Grade	Moligand™
Action Type	ACTIVATOR, GATING INHIBITOR
Mechanism of action	Gating inhibitor of TRPA1;Activator of TRPV1;Activator of TRPV3
Product Description	Camphor is a novel carbon nanotube precursor. Camphor was used in the synthesis of single-walled nanotubes by chemical vapor deposition. It was used in two-phase based hollow fibre liquid-phase microextraction procedure for migration analysis of food packagings containing essential oils.

Associated Targets

RORC Tchem Nuclear receptor ROR-gamma 0 Activities

Discover Target: RORC

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TRPV3 Tchem Transient receptor potential cation channel subfamily V member 3 1 Activities

Discover Target: TRPV3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TRPV1 Tclin Transient receptor potential cation channel subfamily V member 1 0 Activities

Discover Target: TRPV1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 1 Activities

Discover Target: TRPA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

MAPT Tclin Microtubule-associated protein tau 0 Activities

Discover Target: MAPT

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
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
Canonical SMILES	CC1(C2CCC1(C(=O)C2)C)C
Isomeric SMILES	CC1(C2CCC1(C(=O)C2)C)C
WGK Germany	3
RTECS	EX1225000
Alternate CAS	21368-68-3
PubChem CID	2537
UN Number	2717
Packing Group	III
Molecular Weight	152.23
Beilstein	1907611
Reaxy-Rn	1907611

Database links

PubChem CID	2537
ChEBI	CHEBI:36773
CAS Registry No.	76-22-2
Wikipedia	Camphor
ChEMBL Ligand	CHEMBL15768
BindingDB Ligand	50318459
DrugBank Ligand	DB01744
DrugCentral Ligand	470

Certificates

Certificate of Analysis(COA)

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To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

7 results found

Lot Number	Certificate Type	Date	Item
K2320050	Certificate of Analysis	Oct 26, 2023	C110690
K2320053	Certificate of Analysis	Oct 26, 2023	C110690
C23101309	Certificate of Analysis	Mar 16, 2023	C110690
H2224246	Certificate of Analysis	Aug 26, 2022	C110690
J1823094	Certificate of Analysis	Aug 11, 2022	C110690
I2107238	Certificate of Analysis	Sep 11, 2021	C110690
J2312041	Certificate of Analysis	Sep 11, 2021	C110690

Chemical and Physical Properties

Solubility	Solubility in water: 1.5 g/L (20°C) Solubility in other solvents: at 25°C 1 g dissolves in 1 ml Alcohol, 1 ml Ether, 0.5 ml Chloroform, 0.4 ml Benzene, 0.4 ml Acetone, 1.5 ml Turpentine oil, 0.5 ml Glacial acetic acid.
Sensitivity	Moisture sensitive.
Flash Point(°F)	147.2 °F
Flash Point(°C)	65.5℃
Boil Point(°C)	204°C
Melt Point(°C)	175-177°C

Safety and Hazards(GHS)

Pictogram(s)	GHS08, GHS07, GHS02
Signal	Warning
Hazard Statements	H315:Causes skin irritation H319:Causes serious eye irritation H335:May cause respiratory irritation H341:Suspected of causing genetic defects H228:Flammable solid
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P370+P378:In case of fire: Use ... to extinguish. P210:Keep away from heat, hot surface, sparks, open flames and other ignition sources. - No smoking. P302+P352:IF ON SKIN: wash with plenty of water. P321:Specific treatment (see ... on this label). P405:Store locked up. P501:Dispose of contents/container to ... P240:Ground/bond container and receiving equipment. P264:Wash hands [and …] thoroughly after handling. P281:Use personal protective equipment as required. P271:Use only outdoors or in a well-ventilated area. P241:Use explosion-proof [electrical/ventilating/lighting/.../] equipment. P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing. P403+P233:Store in a well-ventilated place. Keep container tightly closed. P362+P364:Take off contaminated clothing and wash it before reuse. P203:Obtain, read and follow all safety instructions before use. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P318:if exposed or concerned, get medical advice. P337+P317:If eye irritation persists: Get medical help. P332+P317:If skin irritation occurs: Get medical help. P319:Get medical help if you feel unwell.
WGK Germany	3
RTECS	EX1225000
Reaxy-Rn	1907611
Class	4.1
Merck Index	1732

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