tirucallol, 514-46-5

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CODE185881 CODE185881
Product(s):
514-46-5 Tirucallol >98%

CAS Number:	514-46-5	3D/inchi
FDA UNII:	Search
Nikkaji Web:	J13.991B
XlogP3-AA:	8.90 (est)
Molecular Weight:	426.72770000
Formula:	C30 H50 O
NMR Predictor:	Predict (works with chrome, Edge or firefox)

Category:natural substances and extractives

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
Google Patents:	Search
US Patents:	Search
EU Patents:	Search
Pubchem Patents:	Search
PubMed:	Search
NCBI:	Search

Physical Properties:

Assay:	95.00 to 100.00
Food Chemicals Codex Listed:	No
Soluble in:
	water, 4.105e-006 mg/L @ 25 °C (est)

Organoleptic Properties:

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

Cosmetic Information:

None found

Suppliers:

Alfa Biotechnology

For experimental / research use only.

Tirucallol 98%

BOC Sciences

For experimental / research use only.

Tirucallol >98%

Carbosynth

For experimental / research use only.

Tirucallol

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:
natural substances and extractives
Recommendation for tirucallol usage levels up to:
	not for fragrance use.

Recommendation for tirucallol flavor usage levels up to:
	not for flavor use.

Safety References:

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 :101257

National Institute of Allergy and Infectious Diseases:Data

(3S,5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

Chemidplus:0000514465

References:

	(3S,5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	101257
Pubchem (cas):	514-46-5

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
HMDB (The Human Metabolome Database):	HMDB37032
FooDB:	FDB016013
VCF-Online:	VCF Volatile Compounds in Food
ChemSpider:	View

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

	argania spinosa Search Trop Picture
	glycine max seed Search Trop Picture
	pistacia lentiscus fruit Search Trop Picture
	synadenium grantii Search Trop Picture
	treculia africana seed Search Trop Picture

Synonyms:

20-epi-	euphol
	lanosta-8,24-dien-3-ol, (3beta,13alpha,14beta,17alpha,20S)-
(3S,5R,10S,13S,14S,17S)-4,4,10,13,14-	pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

Articles:

PubMed:Topical anti-inflammatory effect of tirucallol, a triterpene isolated from Euphorbia lactea latex.

PubMed:Chios mastic gum extract and isolated phytosterol tirucallol exhibit anti-inflammatory activity in human aortic endothelial cells.

PubMed:An isopimarane diterpene from Euphorbia ebracteolata Hayata.

PubMed:Studies in the Chemical Constituents of Azadirachta indica Part II: Isolation and Structure of the New Triterpenoid Azadirachtol.

PubMed:Rotational isomerism about the 17(20)-bond of steroids and euphoids as shown by the crystal structures of euphol and tirucallol.

PubMed:[Studies on the constituents of Chinese drug "kanzui." 8. KMnO4 oxidation of euphol, tirucallol and beta-euphorbol].

Notes:

None found

tirucallol 20-epi-euphol

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Articles:

tirucallol
20-epi-euphol