(Z)-cinnamic acid, 102-94-3

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Name:	(Z)-3-phenylprop-2-enoic acid
CAS Number:	102-94-3	3D/inchi
FDA UNII:	Search
Nikkaji Web:	J1.966F
XlogP3:	2.10 (est)
Molecular Weight:	148.16116000
Formula:	C9 H8 O2
NMR Predictor:	Predict (works with chrome, Edge or firefox)
Also(can) Contains:	cinnamic acid

Category:information only not used for fragrances or flavors

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

Physical Properties:

Appearance:	colorless to aple yellow solid (est)
Assay:	95.00 to 100.00
Food Chemicals Codex Listed:	No
Boiling Point:	265.00 to 266.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure:	0.005000 mmHg @ 25.00 °C. (est)
Flash Point:	373.00 °F. TCC ( 189.50 °C. ) (est)
logP (o/w):	2.412 (est)
Soluble in:
	alcohol
	water, 2911 mg/L @ 25 °C (est)
Insoluble in:
	water

Organoleptic Properties:

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

Cosmetic Information:

None found

Suppliers:

None found

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:
information only not used for fragrances or flavors
Recommendation for (Z)-cinnamic acid usage levels up to:
	not for fragrance use.

Recommendation for (Z)-cinnamic acid 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 :5372954

National Institute of Allergy and Infectious Diseases:Data

(Z)-3-phenylprop-2-enoic acid

Chemidplus:0000102943

References:

	(Z)-3-phenylprop-2-enoic acid
NIST Chemistry WebBook:	Search Inchi
Pubchem (cid):	5372954
Pubchem (sid):	135089904

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
Golm Metabolome Database:	Search
HMDB (The Human Metabolome Database):	HMDB00567
FooDB:	FDB012698
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

cassia bark
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Synonyms:

(Z)-	acidum cinnamylicum
(Z)-	benzene propenoic acid
(Z)-	benzylidene acetic acid
cis-	cinnamic acid
(Z)-	cinnamylic acid
(Z)-3-	phenyl acrylic acid
(Z)-3-	phenyl propenoic acid
(Z)-3-	phenyl propensaeure
(Z)-3-	phenyl-2-propenoic acid
(2Z)-3-	phenylacrylate
(2Z)-3-	phenylprop-2-enoate
(Z)-3-	phenylprop-2-enoic acid

Articles:

Google Patents:Cis-cinnamic acid anti-inflammatory compositions and process of treating inflammation and capillary fragility

PubMed:cis-Cinnamic acid selective suppressors distinct from auxin inhibitors.

PubMed:Design and synthesis of conformationally constrained analogues of cis-cinnamic acid and evaluation of their plant growth inhibitory activity.

PubMed:Substituent effects of cis-cinnamic acid analogues as plant growh inhibitors.

PubMed:Key structural features of cis-cinnamic acid as an allelochemical.

PubMed:A comparative study on the effectiveness of cis- and trans-form of cinnamic acid treatments for inhibiting invasive activity of human lung adenocarcinoma cells.

PubMed:Transformation of cinnamic acid from trans- to cis-form raises a notable bactericidal and synergistic activity against multiple-drug resistant Mycobacterium tuberculosis.

PubMed:Determination of the hydroxycinnamate profile of 12 members of the Asteraceae family.

PubMed:Cis-cinnamic acid-enhanced 1 gene plays a role in regulation of Arabidopsis bolting.

PubMed:Profiling and characterization by LC-MSn of the chlorogenic acids and hydroxycinnamoylshikimate esters in maté (Ilex paraguariensis).

PubMed:Study of cis-cinnamic acid in Arabidopsis thaliana.

PubMed:Plant growth inhibition by cis-cinnamoyl glucosides and cis-cinnamic acid.

PubMed:A comparative vibrational and NMR study of cis-cinnamic acid polymorphs and trans-cinnamic acid.

PubMed:Effect of cis-cinnamic acid and some isomeric compounds on the germination of zygotes of Chlamydomonas.

Notes:

Cinnamic acid is a white crystalline hydroxycinnamic acid, which is slightly soluble in water. It is obtained from oil of cinnamon, or from balsams such as storax. (Wikipedia)

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(Z)-cinnamic acid cis-cinnamic acid

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(Z)-cinnamic acid
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