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Ethyl vanillin

CAS No.
121-32-4
Chemical Name:
Ethyl vanillin
Synonyms
3-ETHOXY-4-HYDROXYBENZALDEHYDE;Rhodiarome;ETHYL VANILIN;Vanirom;FEMA 2464;FEMA 3107;BOURBONAL;ethvlvanillin;ethyl-vanilli;3-Ethoxy-4-hydroxybenzaldehyd
CBNumber:
CB7852934
Molecular Formula:
C9H10O3
Molecular Weight:
166.17
MDL Number:
MFCD00006944
MOL File:
121-32-4.mol
MSDS File:
SDS
Last updated:2025-12-05 14:33:18
Product description Number Pack Size Price
Ethyl vanillin ≥98%, FCC, FG W246409 1 unit $52.72
Ethyl vanillin ≥98%, FCC, FG W246409 1 unit $52.72
Ethyl vanillin ≥98%, FCC, FG W246409 1kg $120
Ethyl vanillin ≥98%, FCC, FG W246409 10Kg $585
3-Ethoxy-4-hydroxybenzaldehyde ReagentPlus , 99% 128090 100g $40
More product size

Ethyl vanillin Properties

Melting point 74-77 °C (lit.)
Boiling point 285°C
Density 1.1097 (rough estimate)
vapor pressure <0.01 mm Hg ( 25 °C)
refractive index 1.4500 (estimate)
FEMA 2464 | ETHYL VANILLIN
Flash point 127°C
storage temp. Store below +30°C.
solubility 2.82g/l
pka 7.91±0.18(Predicted)
form Fine Crystalline Powder
color White to off-white
Odor at 10.00 % in dipropylene glycol. sweet creamy vanilla caramel
Odor Type vanilla
biological source synthetic
Water Solubility slightly soluble
Sensitive Light Sensitive
JECFA Number 893
Merck 14,3859
BRN 1073761
Stability Hygroscopic
LogP 1.58 at 25℃
CAS DataBase Reference 121-32-4(CAS DataBase Reference)
FDA 21 CFR 182.60; 182.90; 582.60
Substances Added to Food (formerly EAFUS) ETHYL VANILLIN
EWG's Food Scores 1
FDA UNII YC9ST449YJ
NIST Chemistry Reference 3-Ethoxy-4-hydroxybenzadehyde(121-32-4)
EPA Substance Registry System Ethyl vanillin (121-32-4)
UNSPSC Code 85151701
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H319
Precautionary statements  P305+P351+P338
Hazard Codes  Xn,Xi
Risk Statements  22-36/37/38
Safety Statements  26-36
WGK Germany  1
RTECS  CU6125000
Hazard Note  Harmful/Irritant/Light Sensitive
TSCA  Yes
HS Code  29124200
Hazardous Substances Data 121-32-4(Hazardous Substances Data)
Toxicity LD50 orally in rats: >2000 mg/kg, P. M. Jenner et al., Food Cosmet. Toxicol. 2, 327 (1964)
NFPA 704
0
2 0

Ethyl vanillin price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W246409 Ethyl vanillin ≥98%, FCC, FG 121-32-4 1 unit $52.72 2025-07-31 Buy
Sigma-Aldrich W246409 Ethyl vanillin ≥98%, FCC, FG 121-32-4 1 unit $52.72 2025-07-31 Buy
Sigma-Aldrich W246409 Ethyl vanillin ≥98%, FCC, FG 121-32-4 1kg $120 2025-07-31 Buy
Sigma-Aldrich W246409 Ethyl vanillin ≥98%, FCC, FG 121-32-4 10Kg $585 2025-07-31 Buy
Sigma-Aldrich 128090 3-Ethoxy-4-hydroxybenzaldehyde ReagentPlus , 99% 121-32-4 100g $40 2025-07-31 Buy
Product number Packaging Price Buy
W246409 1 unit $52.72 Buy
W246409 1 unit $52.72 Buy
W246409 1kg $120 Buy
W246409 10Kg $585 Buy
128090 100g $40 Buy

Ethyl vanillin Chemical Properties,Uses,Production

Overview

Vanillin (4-hydroxy-3-methoxybenzaldehyde) (121-32-4) is the primary chemical component of the extract of vanilla bean. Natural vanilla extract is a mixture of several hundred compounds in addition to vanillin. Artificial vanilla flavoring solution of pure vanillin, is usually of synthetic origin. Synthetic vanillin and ethyl vanillin are used as flavoring agents in foods, beverages, and pharmaceuticals. Ethyl vanillin (3-ethoxy-4-hydroxybenzaldehyde; EVA, Fig. 1) is more expensive and has a stronger flavor. Compared to vanillin, ethyl vanillin has an ethoxy group (-O-CH2CH3) rather than a methoxy group (-O-CH3). The largest single use of ethyl vanillin is for flavoring. It is first synthesized from eugenol found in oil of clove and afterward synthesized from lignincontaining sulfite liquor, a by-product of wood pulp processing in paper manufacture. While some ethyl vanillin is still made from lignin waste, today most synthetic vanillin is synthesized in a two-step process from the petrochemical precursors: vanillin, ethyl vanillin, and guaiacol and, glyoxylic acid. Vanilla, being the world&rsquo;s most popular flavoring materials, finds extensive applications in food, beverages, perfumery and pharmaceutical industry. With the high demand and limited supply of vanilla pods and the continuing increase in their cost, numerous efforts of blending and adulteration in natural vanilla extracts have been reported.
Vanillin
Ethyl vanillin and vanillin, the major phenolic constituents in vanilla products, are widely used as flavoring agents in foods and beverages. Ethyl vanillin, also used as a synthetic compound, is 2.5 times stronger in flavor than vanillin and used to substitute a large amount of vanillin, since it is less expensive and keeps better in storage and transport. Ethyl vanillin is converted to 3-ethoxy4-hydroxybenzaldehyde and 3-ethoxy-4-hydroxymandelic acid after dietary intake[1].

Chemical Properties

WHITE TO OFF-WHITE FINE CRYSTALLINE POWDER

Chemical Properties

White or slightly yellowish crystals with a characteristic intense vanilla odor and flavor.

Chemical Properties

Its odor resembles that of vanillin but is approximately three times as strong. Ethylvanillin can be prepared by method 2 as described for vanillin, using guethol instead of guaiacol as the starting material.

Chemical Properties

Ethyl vanillin has an intense vanilla odor and sweet taste. The flavoring power is two to four times stronger than vanillin. Ethyl vanillin has been used in food since the 1930s; it enhances fruity and chocolate odor impression. Its addition is self-limiting, as too high a level may impart an unpleasant flavor in the product; the product is not stable. In contact with iron or alkali, it exhibits a red color and loses its flavoring power.

Occurrence

Not reported found in nature; it can be distinguished from vanillin because of the yellow color developed in the presence of concentrated H2SO4.

Uses

Ethyl Vanillin, is used as a flavorant, which is about three times as potent as vanillin (V097500) and can be utilized in the production of chocolate. It has also shown to have antioxidant properties.

Uses

Ethyl Vanillin is a flavoring agent that is a synthetic vanilla flavor with approximately three and one-half times the flavoring power of vanillin. it has a solubility of 1 g in 100 ml of water at 50°c. it is used in ice cream, beverages, and baked goods.

Uses

In flavoring and perfumery.

Definition

ChEBI: A member of the class of benzaldehydes that is vanillin in which the methoxy group is replaced by an ethoxy group.

Production Methods

Unlike vanillin, ethyl vanillin does not occur naturally. It may be prepared synthetically by the same methods as vanillin, using guethol instead of guaiacol as a starting material; see Vanillin.

Preparation

From safrole by isomerization to isosafrole and subsequent oxidation to piperonal; the methylene linkage is then broken by heating piperonal in an alcoholic solution of KOH; finally the resulting protocatechualdehyde is reacted with ethyl alcohol. From guaethol by condensation with chloral to yield 3-ethoxy-4-hydroxyphenyl trichloromethyl carbinol; this is then boiled with an alcoholic solution of KOH or NaOH, acidified, and extracted with chloroform to yield ethyl vanillin.

Aroma threshold values

Detection: 100 ppb; recognition: 2 ppm

Taste threshold values

Taste characteristics at 50 ppm: sweet, creamy, vanilla, smooth and caramellic.

Synthesis Reference(s)

The Journal of Organic Chemistry, 44, p. 3305, 1979 DOI: 10.1021/jo01333a006

General Description

Colorless crystals. More intense vanilla odor and taste than vanillin.

Air & Water Reactions

Slightly water soluble .

Reactivity Profile

Protect from light. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation.

Health Hazard

ACUTE/CHRONIC HAZARDS: Toxic. May cause irritation on contact.

Fire Hazard

Combustible

Flammability and Explosibility

Non flammable

Pharmaceutical Applications

Ethyl vanillin is used as an alternative to vanillin, i.e. as a flavoring agent in foods, beverages, confectionery, and pharmaceuticals. It is also used in perfumery.
Ethyl vanillin possesses a flavor and odor approximately three times as intense as vanillin; hence the quantity of material necessary to produce an equivalent vanilla flavor may be reduced, causing less discoloration to a formulation and potential savings in material costs. However, exceeding certain concentration limits may impart an unpleasant, slightly bitter taste to a product due to the intensity of the ethyl vanillin flavor.

Safety Profile

Moderately toxic by ingestion, intraperitoneal, subcutaneous, and intravenous routes. A human skin irritant. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALDEHYDES and ETHERS.

Safety

Ethyl vanillin is generally regarded as an essentially nontoxic and nonirritant material. However, cross-sensitization with other structurally similar molecules may occur.
The WHO has allocated an acceptable daily intake for ethyl vanillin of up to 3 mg/kg body-weight.
LD50 (guinea pig, IP): 1.14 g/kg
LD50 (mouse, IP): 0.75 g/kg
LD50 (rabbit, oral): 3 g/kg
LD50 (rabbit, SC): 2.5 g/kg
LD50 (rat, oral): 1.59 g/kg
LD50 (rat, SC): 3.5–4.0 g/kg

storage

Store in a well-closed container, protected from light, in a cool, dry place. See Vanillin for further information.

Incompatibilities

Ethyl vanillin is unstable in contact with iron or steel, forming a redcolored, flavorless compound. In aqueous media with neomycin sulfate or succinylsulfathiazole, tablets of ethyl vanillin produced a yellow color. See Vanillin for other potential incompatibilities.

Regulatory Status

GRAS listed. Included in the FDA Inactive Ingredients Database (oral capsules, suspensions, and syrups). Included in nonparenteral medicines licensed in the UK.

141-52-6
123-08-0
121-32-4
79459-15-7
Synthesis of Ethyl vanillin from Sodium ethoxide and 4-Hydroxybenzaldehyde
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View Lastest Price from Ethyl vanillin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ethyl Vanillin pictures 2025-12-13 Ethyl Vanillin
121-32-4
US $0.00-0.00 / kg 1kg 99% 20MT Watson Biotechnology Co.,Ltd
Ethyl vanillin pictures 2025-12-13 Ethyl vanillin
121-32-4
US $10.00 / ASSAYS 1ASSAYS 99% 1 ton RongNa Biotechnology Co.,Ltd
Ethyl vanillin pictures 2025-12-13 Ethyl vanillin
121-32-4
US $0.00-0.00 / kg 1kg 99.8% 1000kg WUHAN FORTUNA CHEMICAL CO., LTD
  • Ethyl Vanillin pictures
  • Ethyl Vanillin
    121-32-4
  • US $0.00-0.00 / kg
  • 99%
  • Watson Biotechnology Co.,Ltd
  • Ethyl vanillin pictures
  • Ethyl vanillin
    121-32-4
  • US $10.00 / ASSAYS
  • 99%
  • RongNa Biotechnology Co.,Ltd
  • Ethyl vanillin pictures
  • Ethyl vanillin
    121-32-4
  • US $0.00-0.00 / kg
  • 99.8%
  • WUHAN FORTUNA CHEMICAL CO., LTD
3-ethoxy- 3-Ethoxy-4-hydroxybenzaldehyd 3-ethoxy-4-hydroxy-benzaldehyd 4-Hydroxy-3-ethoxybenzaldehyde Benzaldehyde, 3-ethoxy-4-hydroxy- Benzaldehyde,3-ethoxy-4-hydroxy- Ethavan ethvlvanillin Ethyl protocatechualdehyde AKOS BBS-00003203 AKOS B004185 FEMA 2464 FEMA 3107 ETHYLPROTAL Ethyl protocatechualdehyde 3-ethyl ether ETHYL PROTOCATECHUIC ALDEHYDE ETHYL VANILLIN ETHYL VANILLIN, JAPANESE ETHOVAN BOURBONAL LABOTEST-BB LT00927158 TIMTEC-BB SBB008268 VANILLAL PROTOCATECHUALDEHYDE 3-ETHYL ETHER protocatechualdehyde ethyl ether ETHYL VANILLIN (RHODIAROME) ETHYL VANILLIN 98+% FCC ETHYLVANILLIN(SECONDARY STANDARD) ETHYLVANILLINE ETHYLVANILLIN,NF ethyl pyrocatechuric aldehyde 3-ETHOXY-4-HYDROXYBENZALDEHYDE / ETHYL VANILLIN ETHYLVANILLIN WITH GC ETHYL VANILLIN extrapure 3-ETHOXY-4-HYDROXYBENZALDEHYDE burbonal 3-Ethoxy-4-hydroxybenzaldehyde,97% Ethylvanillin, synthesis grade Ethyl vanillin(FCC4) Ethyl Vanillin (200 mg) 3-Ethoxy-4-Hydroxybenzaldehyde,(S) 3-Ethoxy-4-hydroxybenzaldehyde, 97% 100GR 3-Ethoxy-4-hydroxybenzaldehyde, 97% 5GR ethyl-vanilli Protocatechuic aldehyde 3-ethyl ether protocatechuicaldehydeethylether Quantrovanil Rhodiarome Vanbeenol Vanilal Vanillin, ethyl- Vanirom vanirome ETHYLVANILLIN(SH) 2-Ethoxy-4-formylphenol, Ethyl vanillin 3-Ethoxy-4-hydroxybenzaldehyde ReagentPlus(R), 99% NSC 1803 NSC 67240