Cinnamyl alcohol

Modify Date: 2025-08-19 22:36:44

Cinnamyl alcohol structure	Common Name	Cinnamyl alcohol
	CAS Number	104-54-1	Molecular Weight	134.175
	Density	1.0±0.1 g/cm3	Boiling Point	250.0±0.0 °C at 760 mmHg
	Molecular Formula	C₉H₁₀O	Melting Point	30-33 °C(lit.)
	MSDS	Chinese USA	Flash Point	124.8±14.5 °C
	Symbol	GHS07	Signal Word	Warning

Use of Cinnamyl alcohol

Cinnamyl Alcohol is an active component from chestnut flower, inhibits increased PPARγ expression, with anti-obesity activity[1].

Name	cinnamyl alcohol
Synonym	More Synonyms

Description	Cinnamyl Alcohol is an active component from chestnut flower, inhibits increased PPARγ expression, with anti-obesity activity[1].
Related Catalog	Signaling Pathways >> Cell Cycle/DNA Damage >> PPAR Research Areas >> Metabolic Disease
References	[1]. Hwang DI, et al. Cinnamyl Alcohol, the Bioactive Component of Chestnut Flower Absolute, Inhibits Adipocyte Differentiation in 3T3-L1 Cells by Downregulating Adipogenic Transcription Factors. Am J Chin Med. 2017;45(4):833-846.

Density	1.0±0.1 g/cm3
Boiling Point	250.0±0.0 °C at 760 mmHg
Melting Point	30-33 °C(lit.)
Molecular Formula	C₉H₁₀O
Molecular Weight	134.175
Flash Point	124.8±14.5 °C
Exact Mass	134.073166
PSA	20.23000
LogP	1.70
Vapour density	4.6 (vs air)
Vapour Pressure	0.0±0.5 mmHg at 25°C
Index of Refraction	1.599
Storage condition	2-8°C
Stability	Stable. Incompatible with strong oxidizing agents.
Water Solubility	1.8 g/L (20 ºC)

Cinnamyl alcohol MSDS(Chinese)

CHEMICAL IDENTIFICATION

RTECS NUMBER :: GE2200000

CHEMICAL NAME :: Cinnamyl alcohol

CAS REGISTRY NUMBER :: 104-54-1

BEILSTEIN REFERENCE NO. :: 1903999

LAST UPDATED :: 199701

DATA ITEMS CITED :: 10

MOLECULAR FORMULA :: C9-H10-O

MOLECULAR WEIGHT :: 134.19

WISWESSER LINE NOTATION :: Q2U1R

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: Standard Draize test

ROUTE OF EXPOSURE :: Administration onto the skin

SPECIES OBSERVED :: Rodent - rabbit

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - rat

DOSE/DURATION :: 2 gm/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 2675 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Administration onto the skin

SPECIES OBSERVED :: Rodent - rabbit

DOSE/DURATION :: >5 gm/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - guinea pig

DOSE/DURATION :: 2675 mg/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

TYPE OF TEST :: TDLo - Lowest published toxic dose

ROUTE OF EXPOSURE :: Oral

SPECIES OBSERVED :: Rodent - rat

DOSE/DURATION :: 6366 mg/kg/17W-I

TOXIC EFFECTS :: Blood - changes in serum composition (e.g. TP, bilirubin, cholesterol) Biochemical - Enzyme inhibition, induction, or change in blood or tissue levels - other Enzymes

MUTATION DATA

TYPE OF TEST :: DNA repair

TEST SYSTEM :: Bacteria - Bacillus subtilis

DOSE/DURATION :: 10 mg/disc

REFERENCE :: OIGZDE Osaka-shi Igakkai Zasshi. Journal of Osaka City Medical Association. (Osaka-shi Igakkai, c/o Osaka-shiritsu Daigaku Igakubu, 1-4-54 Asahi-cho, Abeno-ku, Osaka, 545, Japan) V.24- 1975- Volume(issue)/page/year: 34,267,1985 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - 83181 No. of Facilities: 163 (estimated) No. of Industries: 6 No. of Occupations: 36 No. of Employees: 8942 (estimated) NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - 83181 No. of Facilities: 4817 (estimated) No. of Industries: 25 No. of Occupations: 48 No. of Employees: 76974 (estimated) No. of Female Employees: 43896 (estimated)

Symbol	GHS07
Signal Word	Warning
Hazard Statements	H302-H315-H317-H319
Precautionary Statements	P280-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US);Eyeshields;Faceshields;Gloves
Hazard Codes	Xn:Harmful
Risk Phrases	R22;R36;R43
Safety Phrases	S26-S36/37-S37/39-S24
RIDADR	2811
WGK Germany	2
RTECS	GE2200000
Hazard Class	6.1
HS Code	2912299000

Precursor 9
CAS#:1504-58-1 3-Phenyl-2-prop... CAS#:4393-06-0 3-Phenylpropene-3-ol CAS#:88738-40-3 Benzene, [(1E)-... CAS#:104-55-2 Cinnamaldehyde
CAS#:621-82-9 Cinnamic acid CAS#:103-36-6 Ethyl cinnamate CAS#:109283-53-6 (3-phenyl-prop-... CAS#:71700-50-0 tert-butyl-dime...
CAS#:102-92-1 Ciprofloxacin H...
DownStream 9
CAS#:111944-30-0 bis(3-phenylpro... CAS#:4393-06-0 3-Phenylpropene-3-ol CAS#:4392-24-9 Cinnamyl bromide CAS#:1456-19-5 1H-Benzimidazol...
CAS#:2243-52-9 (E)-4-(4-NITROP... CAS#:292638-84-7 phenylene-ethylene CAS#:637-50-3 β-Methylstyrene CAS#:104-55-2 Cinnamaldehyde
CAS#:63576-88-5

HS Code	2912299000
Summary	2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

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Comprehensive two-dimensional gas chromatography (GC×GC) coupled with Mass Spectrometry (MS) is one of today's most powerful analytical platforms for detailed analysis of medium-to-high complexity sam...

Functional characterization of two acyltransferases from Populus trichocarpa capable of synthesizing benzyl benzoate and salicyl benzoate, potential intermediates in salicinoid phenolic glycoside biosynthesis.

Phytochemistry 113 , 149-59, (2015)

Salicinoids are phenolic glycosides (PGs) characteristic of the Salicaceae and are known defenses against insect herbivory. Common examples are salicin, salicortin, tremuloidin, and tremulacin, which ...

Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage.

Bioorg. Med. Chem. 19 , 2392-6, (2011)

In our previous paper, we reported that rosmarinic acid (1) of Argusia argentea could neutralize snake venom induced hemorrhagic action. Rosmarinic acid (1) consists of two phenylpropanoids: caffeic a...

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