hinokiol, 564-73-8

Supplier Sponsors

Best of Chemicals Supplier
Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
Email:	Marketing
US Email:	Marketing
Email:	Sales
US Email:	Sales
Voice: 1-631-485-4226
Fax: 1-631-614-7828
US Voice: 1-631-485-4226
US Fax: 1-631-614-7828
Europe	44-203-286-1088
Facebook
Twitter
Linkedin
Blog
Get the App!
CODE106386 CODE106386
Product(s):
564-73-8 Hinokiol
Hinokiol is extracted from the barks of Cephalotaxus fortunei Hook. f. It inhi

CAS Number:	564-73-8	3D/inchi
FDA UNII:	Search
Nikkaji Web:	J16.963C
XlogP3-AA:	5.20 (est)
Molecular Weight:	302.45750000
Formula:	C20 H30 O2
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
Boiling Point:	427.00 °C. @ 760.00 mm Hg (est)
Flash Point:	374.00 °F. TCC ( 189.90 °C. ) (est)
logP (o/w):	5.930 (est)
Soluble in:
	water, 1.83 mg/L @ 25 °C (est)

Organoleptic Properties:

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

Cosmetic Information:

None found

Suppliers:

BOC Sciences

For experimental / research use only.

Hinokiol

Odor: characteristic

Use: Hinokiol is extracted from the barks of Cephalotaxus fortunei Hook. f. It inhi

Coompo

For experimental / research use only.

Hinokiol from Plants ≥96%

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 hinokiol usage levels up to:
	not for fragrance use.

Recommendation for hinokiol 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 :12310492

National Institute of Allergy and Infectious Diseases:Data

(2S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol

References:

	(2S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	12310492
Pubchem (sid):	319350325

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
CHEMBL:	View
HMDB (The Human Metabolome Database):	Search
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

found in nature

Synonyms:

(3b)-	abieta-8,11,13-triene-3,12-diol
2,6-	phenanthrenediol, 1,2,3,4,4a,9,10,10a-octahydro-1,1,4a-trimethyl-7-(1-methylethyl)-, (2S,4aS,10aR)-
	podocarpa-8,11,13-triene-3β,12-diol, 13-isopropyl-
(2S,4aS,10aR)-1,1,4a-	trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol

Articles:

PubMed:Diterpenoids with anti-inflammatory activity from the wood of Cunninghamia konishii.

PubMed:Abietane diterpenoids from Isodon lophanthoides var. graciliflorus and their cytotoxicity.

PubMed:Antibacterial activity of Taxodium ascendens diterpenes against methicillin-resistant Staphylococcus aureus.

PubMed:Abietane diterpenoids from Isodon lophanthoides var. graciliflorus and their cytotoxicity.

PubMed:Terpenoids from Juniperus procera with hepatoprotective activity.

PubMed:[Quantitative analysis of hinokiol from cell suspension cultures of Cephalotaxus fortunei].

PubMed:The anti-inflammatory activities of an extract and compounds isolated from Platycladus orientalis (Linnaeus) Franco in vitro and ex vivo.

PubMed:seco-Abietane diterpenoids, a phenylethanoid derivative, and antitubercular constituents from Callicarpa pilosissima.

PubMed:Discriminating the indistinguishable sapwood from heartwood in discolored ancient wood by direct molecular mapping of specific extractives using time-of-flight secondary ion mass spectrometry.

PubMed:Terpenoids and phenolics from Plectranthus strigosus, bioactivity screening.

PubMed:seco-Hinokiol, a new abietane diterpenoid from Rosmarinus officinalis.

Notes:

None found

hinokiol podocarpa-8,11,13-triene-3β,12-diol, 13-isopropyl-

Supplier Sponsors

Articles:

hinokiol
podocarpa-8,11,13-triene-3β,12-diol, 13-isopropyl-