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(1R)-(-)-Thiocamphor

(1R)-(-)-Thiocamphor Structure
(1R)-(-)-Thiocamphor structure
CAS No.
53402-10-1
Chemical Name:
(1R)-(-)-Thiocamphor
Synonyms
(1R)-(-)-Thiocamphor;(1R)-(-)-Thiocamphor;(1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2-thione;(1r)-(-)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-thione;Bicyclo[2.2.1]heptane-2-thione, 1,7,7-trimethyl-, (1R,4R)-
CBNumber:
CB7169504
Molecular Formula:
C10H16S
Molecular Weight:
168.3
MDL Number:
MFCD00074855
MOL File:
53402-10-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:54:42
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(1R)-(-)-Thiocamphor Properties

Melting point 136-138 °C(lit.)
Boiling point 228-230 °C(lit.)
Density 0.9691 (rough estimate)
refractive index 1.6500 (estimate)
form powder to crystal
color Light yellow to Brown

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
Signal word  Warning
Hazard statements  H228-H302+H312+H332-H315-H319
Precautionary statements  P210-P240-P241-P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P305+P351+P338+P337+P313-P501
Hazard Codes  F,Xi
Risk Statements  11-36/37/38
Safety Statements  16-26-36
RIDADR  UN 1325 4.1/PG 3
WGK Germany  3
HS Code  2930.90.9250
HazardClass  4.1
PackingGroup  III
NFPA 704
0
2 0

(1R)-(-)-Thiocamphor price More Price(9)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical T1863 (1R)-(-)-Thiocamphor >97.0%(GC) 53402-10-1 1g $94 2026-04-30 Buy
TCI Chemical T1863 (1R)-(-)-Thiocamphor >97.0%(GC) 53402-10-1 5g $286 2026-04-30 Buy
Chem-Impex 39147 (1R)-(-)-Thiocamphor ≥97%(GC) 53402-10-1 1G $137.41 2026-05-19 Buy
Chem-Impex 39147 (1R)-(-)-Thiocamphor ≥97%(GC) 53402-10-1 5G $459.29 2026-05-19 Buy
aablocks AA003BCY (1R)-(-)-Thiocamphor 95% 53402-10-1 250mg $74 2026-05-28 Buy
Product number Packaging Price Buy
T1863 1g $94 Buy
T1863 5g $286 Buy
39147 1G $137.41 Buy
39147 5G $459.29 Buy
AA003BCY 250mg $74 Buy

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

Purification Methods

It forms red prisms from EtOH and sublimes under vacuum. It possesses a sulfurous odour and is volatile like camphor. [Sen J Indian Chem Soc 12 647 1935, Sen J Indian Chem Soc 18 76 1941.] The racemate crystallises from *C6H6 and has m 145o [138.6-139o, White & Bishop J Am Chem Soc 62 10 1940]. [Beilstein 7 III 419.]

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

Raw materials

Preparation Products

(1R)-(-)-Thiocamphor Suppliers

Global Suppliers ( 34)
Supplier Tel Email Country ProdList Advantage
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Shanghai Longsheng chemical Co.,Ltd. 58099637 13585536065 sales@shlschem.com China 9880 59
TOKYO CHEMICAL INDUSTRY CO., LTD. 03-36680489 Sales-JP@TCIchemicals.com Japan 28364 80
9ding chemical ( Shanghai) Limited 4009209199 sales@9dingchem.com China 22497 55
Chengdu Huachun Technology Co., Ltd 400-1166-196 15982826727 cdhxsj@163.com China 14571 60
Aikon International Limited 025-66113011 19370895928 qzhang@aikonchem.com China 15390 58
Beijing Minruida Technology Co., Ltd. 010-82387566 sales@mreda.com.cn China 19323 58
Supplier Advantage
J & K SCIENTIFIC LTD. 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 62
TCI (Shanghai) Development Co., Ltd. 81
Energy Chemical 61
Shanghai Longsheng chemical Co.,Ltd. 59
TOKYO CHEMICAL INDUSTRY CO., LTD. 80
9ding chemical ( Shanghai) Limited 55
Chengdu Huachun Technology Co., Ltd 60
Aikon International Limited 58
Beijing Minruida Technology Co., Ltd. 58

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(1r)-(-)-1,7,7-trimethylbicyclo[2.2.1]heptane-2-thione (1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2-thione (1R)-(-)-Thiocamphor Bicyclo[2.2.1]heptane-2-thione, 1,7,7-trimethyl-, (1R,4R)- (1R)-(-)-Thiocamphor 53402-10-1 Organic Building Blocks Thiocarbonyl Compounds Chiral Building Blocks Asymmetric Synthesis Terpenes Bicyclic Monoterpenes Biochemistry Terpenes Bicyclic Monoterpenes