lenthionine, 292-46-6

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CODE157692 CODE157692
Product(s):
292-46-6 1,2,3,5,6-Pentasulfur-cycloheptane 95%

M&U International LLC

Steady supply & demand
Meeting customers increasing demands at home as well as abroad.
M&U dedicates itself to the development and production of new products as well as continuously promoting those new products. We’ve maintained a steady supply&demand relationship with a large number of manufacturers at home and abroad. We’ve developed an extensive network and because of our relationships with these manufacturers, we’re able to provide a stable supply of great quality materials. We’re located in China’s largest communications hub, Shanghai and in the U.S. near one of the largest sea ports on the East Coast. The strategic locations of our facilities ensure convenient, prompt and secure delivery of our products to our customers.
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CODE157692 CODE157692
Product(s):
H0190 1,2,3,5,6-PENTASULFUR-CYCLOHEPTANE, Kosher

Sunaux International

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We have industry leading processes and procedures to ensure nothing but the most reliable product.
Sunaux International was founded in 2012 by the owner Mr.John Felton after spending 18 years involved in developing global business in the aromatic chemicals, fragrance and flavour compounds business.
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CODE157692 CODE157692
Product(s):
H0189 1,2,3,5,6-Pentasulfur-cycloheptane

CAS Number:	292-46-6	3D/inchi
FDA UNII:	71G9U1CIRD
Nikkaji Web:	J5.458E
MDL:	MFCD03840531
CoE Number:	11619
XlogP3-AA:	2.00 (est)
Molecular Weight:	188.37888000
Formula:	C2 H4 S5
BioActivity Summary:	listing
NMR Predictor:	Predict (works with chrome, Edge or firefox)

Category:flavoring agents

US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:

Google Scholar:	Search
Google Books:	Search
Google Scholar: with word "volatile"	Search
Google Scholar: with word "flavor"	Search
Google Scholar: with word "odor"	Search
Perfumer and Flavorist:	Search
Google Patents:	Search
US Patents:	Search
EU Patents:	Search
Pubchem Patents:	Search
PubMed:	Search
NCBI:	Search
DG SANTE Food Flavourings:	15.081 lenthionine

Physical Properties:

Assay:	95.00 to 100.00
Food Chemicals Codex Listed:	No
Melting Point:	61.00 °C. @ 760.00 mm Hg
Boiling Point:	287.00 °C. @ 760.00 mm Hg
Vapor Pressure:	0.000082 mmHg @ 25.00 °C. (est)
Flash Point:	374.00 °F. TCC ( 190.00 °C. )
logP (o/w):	4.238 (est)
Soluble in:
	alcohol
	water, 532.7 mg/L @ 25 °C (est)
Insoluble in:
	water

Organoleptic Properties:

Odor Description:mushroom

Odor and/or flavor descriptions from others (if found).

Cosmetic Information:

None found

Suppliers:

BOC Sciences

For experimental / research use only.

1,2,3,5,6-Pentasulfur-cycloheptane 95%

Carbosynth

For experimental / research use only.

Lenthionine

Jinan Enlighten Chemical Technology(Wutong Aroma )

1,2,3,5,6-Pentasulfur-cylloheptane(Shiitake)

M&U International

1,2,3,5,6-PENTASULFUR-CYCLOHEPTANE, Kosher

Matrix Scientific

For experimental / research use only.

1,2,3,5,6-Pentathiepane, 95+%

sds

Sunaux International

1,2,3,5,6-Pentasulfur-cycloheptane

Safety Information:


Hazards identification

Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements

Pictogram

Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined

Safety in Use Information:

Category:
flavoring agents
Recommendation for lenthionine usage levels up to:
	not for fragrance use.

Maximised Survey-derived Daily Intakes (MSDI-EU):		0.012 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI):		78 (μg/person/day)
Threshold of Concern:		90 (μg/person/day)
Structure Class:		III

Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
		average usage mg/kg	maximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0):		0.20000	1.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0):		0.10000	0.50000
Edible ices, including sherbet and sorbet (03.0):		0.20000	1.00000
Processed fruit (04.1):		0.20000	1.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2):		-	-
Confectionery (05.0):		0.20000	1.00000
Chewing gum (05.3):		-	-
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0):		0.10000	0.50000
Bakery wares (07.0):		0.20000	1.00000
Meat and meat products, including poultry and game (08.0):		0.10000	0.20000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0):		0.10000	0.20000
Eggs and egg products (10.0):		-	-
Sweeteners, including honey (11.0):		-	-
Salts, spices, soups, sauces, salads, protein products, etc. (12.0):		0.10000	0.50000
Foodstuffs intended for particular nutritional uses (13.0):		-	-
Non-alcoholic ("soft") beverages, excl. dairy products (14.1):		0.10000	0.30000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2):		0.20000	1.00000
Ready-to-eat savouries (15.0):		0.40000	2.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0):		0.10000	0.50000

Safety References:

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

Flavouring Group Evaluation 8 (FGE.08)[1]: Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical group 20
View page or View pdf

Flavouring Group Evaluation 74 (FGE.74)[1]: Consideration of Simple Aliphatic Sulphides and Thiols evaluated by JECFA (61st meeting) Structurally related to Aliphatic and Alicyclic Mono-, Di-, Tri-, and Polysulphides with or without Additional Oxygenated Functional Groups from Chemical Group 20 evaluated by EFSA in FGE.08 (2008)
View page or View pdf

Flavouring Group Evaluation 8, Revision 1 (FGE.08Rev1): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30
View page or View pdf

Flavouring Group Evaluation 91 (FGE.91): Consideration of simple aliphatic and aromatic sulphides and thiols evaluated by JECFA (53rd and 68th meetings) structurally related to aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups evaluated by EFSA in FGE.08Rev1 (2009)
View page or View pdf

Flavouring Group Evaluation 08 Rev2 (FGE.08 Rev2): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 8, Revision 3 (FGE.08Rev3): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 08, Revision 4 (FGE.08Rev4): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 08, Revision 5 (FGE.08Rev5): Aliphatic and alicyclic mono-, di-, tri-, and polysulphides with or without additional oxygenated functional groups from chemical groups 20 and 30
View page or View pdf

EPI System: View

AIDS Citations:Search

Cancer Citations:Search

Toxicology Citations:Search

EPA ACToR:Toxicology Data

EPA Substance Registry Services (SRS):Registry

Laboratory Chemical Safety Summary :67521

National Institute of Allergy and Infectious Diseases:Data

1,2,3,5,6-pentathiepane

Chemidplus:0000292466

References:

	1,2,3,5,6-pentathiepane
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	67521
Pubchem (sid):	135024285

Other Information:

(IUPAC):	Atomic Weights of the Elements 2011 (pdf)
Videos:	The Periodic Table of Videos
tgsc:	Atomic Weights use for this web site
(IUPAC):	Periodic Table of the Elements
CHEBI:	View
KEGG (GenomeNet):	C08382
HMDB (The Human Metabolome Database):	HMDB31258
FooDB:	FDB003295
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View
Wikipedia:	View

Potential Blenders and core components note

None Found

Potential Uses:

mushroom

Occurrence (nature, food, other):note

mushroom shiitake mushroom
Search PMC Picture

Synonyms:

1,2,3,5,6-

pentathiepane

Articles:

PubMed:Contributions of non-volatile and volatile compounds to the umami taste and overall flavour of shiitake mushroom extracts and their application as flavour enhancers in cooked minced meat.

PubMed:A scent of therapy: pharmacological implications of natural products containing redox-active sulfur atoms.

PubMed:Mini-laparotomy for repair of infrarenal abdominal aortic aneurysm.

PubMed:Inhibitory activity of shiitake flavor against platelet aggregation.

PubMed:The influence of Lentinus edodes (Shiitake mushroom) preparations on bacteriological and morphological aspects of the small intestine in piglets.

PubMed:Encapsulation of shiitake (Lenthinus edodes) flavors by spray drying.

PubMed:Antibacterial effect of the culture fluid of Lentinus edodes mycelium grown in submerged liquid culture.

PubMed:Degradation of L-djenkolate catalyzed by S-alkylcysteine alpha,beta-lyase from Pseudomonas putida.

PubMed:The red algal-higher fungi phylogenetic link: the last ten years.

PubMed:Isolation, structure, and synthesis of lenthionine and its analogs.

Notes:

Constit. of the edible mushroom Shiitake (Lentinus edodes), responsible for its characteristic odour. Also a volatile prod. of cooked mutton. Also isol. from petai (Parkia speciosa)

lenthionine 1,2,3,5,6-pentathiepane

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lenthionine
1,2,3,5,6-pentathiepane