2,5-dimethoxy-4-benzoquinone, 3117-03-1

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CODE136017 CODE136017
Product(s):
D2250 2,5-Dimethoxy-4-benzoquinone >98.0%(GC)
SDS

Name:	2,5-dimethoxycyclohexa-2,5-diene-1,4-dione
CAS Number:	3117-03-1	3D/inchi
FDA UNII:	XJL7OE03FS
Nikkaji Web:	J80.641B
MDL:	MFCD00189386
XlogP3:	-0.10 (est)
Molecular Weight:	168.14856000
Formula:	C8 H8 O4
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
PubMed:	Search
NCBI:	Search

Physical Properties:

Assay:	95.00 to 100.00
Food Chemicals Codex Listed:	No
Soluble in:
	water, 8.794e+004 mg/L @ 25 °C (est)

Organoleptic Properties:

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

Cosmetic Information:

None found

Suppliers:

Santa Cruz Biotechnology

For experimental / research use only.

2,5-Dimethoxy-4-benzoquinone

Sigma-Aldrich: Aldrich

For experimental / research use only.

2,5-DIMETHOXY-(1,4)BENZOQUINONE

sds

TCI AMERICA

For experimental / research use only.

2,5-Dimethoxy-4-benzoquinone >98.0%(GC)

sds

Safety Information:

Preferred SDS: View

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 2,5-dimethoxy-4-benzoquinone usage levels up to:
	not for fragrance use.

Recommendation for 2,5-dimethoxy-4-benzoquinone 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

National Institute of Allergy and Infectious Diseases:Data

2,5-dimethoxycyclohexa-2,5-diene-1,4-dione

Chemidplus:0003117031

References:

	2,5-dimethoxycyclohexa-2,5-diene-1,4-dione
NIST Chemistry WebBook:	Search Inchi
Pubchem (cas):	3117-03-1

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
KEGG (GenomeNet):	C01692
HMDB (The Human Metabolome Database):	HMDB34335
FooDB:	FDB012694
Export Tariff Code:	2914.69.9000
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

	calamus Search Trop Picture
	plumeria rubra bark Search Trop Picture

Synonyms:

p-	benzoquinone, 2,5-dimethoxy- (8CI)
2,5-	cyclohexadiene-1,4-dione, 2,5-dimethoxy- (9CI)
2,5-	dimethoxy-2,5-cyclohexadiene-1,4-dione
2,5-	dimethoxycyclohexa-2,5-diene-1,4-dione

Articles:

PubMed:A new sesquiterpene lactone from the roots of Lasianthus acuminatissimus.

PubMed:Heritable variation in quinone-induced haustorium development in the parasitic plant Triphysaria.

PubMed:Cytotoxic constituents of the bark of Plumeria rubra collected in Indonesia.

PubMed:Site of electron acceptance by 3,6-dichloro-2,5-dimethoxy-p-benzoquinone and its relation to the bicarbonate effect on photosynthetic electron transport.

Notes:

Isol. from Acorus calamus (sweet flag) Disulfiram produces a sensitivity to alcohol which results in a highly unpleasant reaction when the patient under treatment ingests even small amounts of alcohol. Disulfiram blocks the oxidation of alcohol at the acetaldehyde stage during alcohol metabolism following disulfiram intake, the concentration of acetaldehyde occurring in the blood may be 5 to 10 times higher than that found during metabolism of the same amount of alcohol alone. Accumulation of acetaldehyde in the blood produces a complex of highly unpleasant symptoms referred to hereinafter as the disulfiram-alcohol reaction. This reaction, which is proportional to the dosage of both disulfiram and alcohol, will persist as long as alcohol is being metabolized. Disulfiram does not appear to influence the rate of alcohol elimination from the body. Prolonged administration of disulfiram does not produce tolerance

2,5-dimethoxy-4-benzoquinone p-benzoquinone, 2,5-dimethoxy- (8CI)

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Articles:

2,5-dimethoxy-4-benzoquinone
p-benzoquinone, 2,5-dimethoxy- (8CI)