PRODUCTS

Ethyl Vanillin

ETHYL VANILLIN

Ethyl vanillin = Bourbonal = 3-Ethoxy-4-hydroxybenzaldehyde = Ethylvanillin

CAS Number = 121-32-4
EC Number = 204-464-7
NSC Number = 67240

Molecular Weight   166.17 2.1
XLogP3   1.6   Computed by XLogP3 3.0
Hydrogen Bond Donor Count   1
Hydrogen Bond Acceptor Count   3
Rotatable Bond Count   3
Exact Mass   166.062994177 2.1
Monoisotopic Mass   166.062994177 2.1
Topological Polar Surface Area   46.5 Å²
Heavy Atom Count   12
Formal Charge   0
Complexity   147
Isotope Atom Count   0
Defined Atom Stereocenter Count   0
Undefined Atom Stereocenter Count   0
Defined Bond Stereocenter Count   0
Undefined Bond Stereocenter Count   0
Covalently-Bonded Unit Count   1
Compound Is Canonicalized   Yes
Taste of Ethyl Vanillin = Sweet
Boiling Point of Ethyl Vanillin = 294.0 °C
Melting Point of Ethyl Vanillin = 171 to 172 °F
Flash Point of Ethyl Vanillin = 145 °C (293 °F)
Solubility of Ethyl Vanillin = Slightly soluble
Vapor Pressure of Ethyl Vanillin = 1.04e-05 mmHg
LogP of Ethyl Vanillin = 1.58
Decomposition of Ethyl Vanillin = When heated to decomposition it emits acrid smoke and irritating fumes.
pH of Ethyl Vanillin = Solutions are acid to litmus
Molecular Formula of Ethyl Vanillin = C9H10O3
Canonical SMILES of Ethyl Vanillin = CCOC1=C(C=CC(=C1)C=O)O

Ethyl vanillin appears as colorless crystals. More intense vanilla odor and taste than vanillin.

Ethylvanillin is the organic compound with the formula (C2H5O)(HO)C6H3CHO.
This colorless solid consists of a benzene ring with hydroxyl, ethoxy, and formyl groups on the 4, 3, and 1 positions, respectively.

An extremely sweet and creamy aromatic chemical, Ethyl Vanillin is a crystalline powder that is aromatically compatible with a huge range of other ingredients, making it highly versatile for both flavor and fragrance purposes.
Warm and intensely reminiscent of vanilla, this chemical is incredibly tenacious when added to flavoring mixtures, making it a must-have for many different fruit and dairy products.
The subtle, lightly floral nuances of its odor also makes it a popular choice among gourmand perfumery.
ethyl vanillin A synthetic compound, chemically the ethyl analogue of vanillin, the major flavouring principle of vanilla.

C2H5O(OH)C6H3CHO A compound, crystallizing in fine white crystals that melt at 76.5°C, has a strong vanilla odor and four times the flavor of vanilla, soluble in organic solvents such as alcohol, chloroform, and ether; used in the food industry as a flavoring agent to replace or fortify vanilla.

Ethyl vanillin is an artificial taste agent derived from vanillin, out there as fine white to a barely yellow crystal.
Bourbonal has a lot stronger taste than vanillin.
Bourbonal is the organic compound with the formula (C2H5O)(HO)C6H3CHO.
Ethyl vanillin is broadly accepted as protected meals additive in lots of nations.
This colorless solid consists of a benzene ring with ethoxy, hydroxyl and formyl groups on the 4, 3, and 1 position.
Bourbonal comes as white to cream colored crystal powder.
Ethyl vanillin is a synthetic molecule not found in nature.

AROMA & FLAVOR OF ETHYL VANILLIN
Incredibly creamy and sweet, with a powerful flavor heavily reminiscent of vanilla.
Also contains lightly floral undertones that add gourmand notes to fragrances.

Ethyl vanillin, also known as bourbonal or ethyl protal, belongs to the class of organic compounds known as hydroxybenzaldehydes.
These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.
Ethyl vanillin is a sweet, caramel, and creamy tasting compound.
Based on a literature review a significant number of articles have been published on Ethyl vanillin.

Ethyl vanillin, also called as Ethylvanillin, appears white to off-white fine crystalline powder.
It has similar but stronger scent than vanillin.
Ethylvanillin is prepared from catechol, beginning with ethylation to give guethol.
Ethylvanillin is used in the formulation fragrance and flavor.

Vanillin is an organic compound with the formula C8H8O3.
Bourbonal is the primary component of the vanilla bean.
Vanillin is used in perfumes and fragrances in both cleaning products and candles, in the food industry to flavor chocolate, baked goods, and ice cream, and in medicines to mask unpleasant flavors.
Ethylvanillin - also used in the food industry - has a stronger scent, is more expensive, and differs slightly in it's chemistry.
Vanillin accounts for roughly 2 percent of the dry weight of cured vanilla beans, and is the primary flavor component found in vanilla beans.

Ethyl vanillin is a member of the class of benzaldehydes that is vanillin in which the methoxy group is replaced by an ethoxy group.
Bourbonal has a role as an antioxidant and a flavouring agent.
Bourbonal is a member of benzaldehydes, a member of phenols and an aromatic ether.
Bourbonal derives from a vanillin.

Vanilla flavor is used in a wide variety of products, especially in the production of chocolate and chocolate drinks.
Natural vanilla with its unrivaled bouquet is used in high-grade confectionery (most products are currently flavored with synthetic vanillin and ethyl-vanillin).

Ethyl Vanillin (C9H10O3) is a fine white or sometimes slightly yellow crystalline needle or colorless flakes.
Two key industries that use ethyl vanillin are flavoring and perfumery, with flavoring being the primary way that most of the general population comes into contact with the product.

Ethylvanillin is simply vanillin with an extra carbon - a methoxy becomes and ethoxy.
Bourbonals preparation parallels that of synthetic vanillin, simply introducing that extra carbon at the beginning of the process, starting from guethol instead of guaiacol

Overview for Ethyl Vanillin:
Vanillin (4-hydroxy-3-methoxybenzaldehyde) 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) 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.
Bourbonal 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’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.

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.

Ethyl Vanillin is a fine powder with three times more potency than Vanillin and offers a more concentrated flavor profile in order to provide sweet, pure and rich creamy notes of vanilla.

General description
Ethyl vanillin is one of the main components of artificial vanilla flavorings.
Bourbonal is also used a flavor enhancer.

Ethyl vanillin is a phenolic compound substituted to form ethyl vanillin.
As the name suggests, it is a fine white or yellowish crystalline powder.
Bourbonal can be considered a synthetic vanilla flavor.
Bourbonal has slightly more potent vanilla flavor than vanillin alone.

Ethyl vanillin (bourbonal, vanillose).
Ethylvaniline (C6N3ON • OS2N5-CHO) is vanillin, in which the methyl group of vanillin is replaced by ethyl.
Although ethyl-vanillin has been known for many years, the complexity of its preparation without unpleasant impurities hampered its sales, but a quite acceptable product is currently being manufactured and widely used.
The use of ethyl valaniline is economically viable, since it is claimed that it is five times stronger, but only four times more expensive than vanillin. Ethylaniline smells a little different from vanillin, but in most of the tasting tests described above this difference is not found.

The choice of good vanilla beans requires experience.
Once it was considered important to have vanillin crystals on the surface, but we once encountered a falsification - sprinkling pods with crystals of benzoic acid.
The only correct method to evaluate the quality is to prepare an alcohol extract and flavor them with a fondant.

Vanilla extract is prepared by slicing the grain into small pieces and soaking them successively in batches of hot 65-70% strength alcohol.
So you can ensure obtaining natural vanilla flavor.
Currently there are many commercially available extracts, representing a mixture of natural and synthetic products.

Ethyl Vanillin Soluble in:
chloroform
ethyl alcohol, 1gm. in 3cc of 95% alcohol at 32F
ethyl alcohol, 2 vol. 95% alcohol
ethyl alcohol, 4.81 g. in 100ml. 80% propylene glycol/ 20% water by volume at 77
fixed oils
glycerin
propylene glycol
water, 2867 mg/L @ 25 °C (est)
water, 2820 mg/L @ 25 °C (exp)

Organoleptic Properties of Ethyl Vanillin
Odor Type: vanilla
biological source: synthetic
Odor Strength:medium
recommend smelling in a 10.00 % solution or less
Substantivity:400 hour(s) at 20.00 % in dipropylene glycol
sweet creamy vanilla caramellic
Odor Description:at 10.00 % in dipropylene glycol. sweet creamy vanilla caramel
Odor sample from: Berje Inc.
sweet creamy vanilla root beer
Odor Description:Sweet, creamy, vanilla, with a root berry salicylate-like nuance

Ethylvanillin vs. vanillin
Since vanilla and vanillin are both quite scarce, people have been looking for cheaper alternatives for decades.
Hence, you might have heard of ethylvanillin as well.
This isn’t the ‘regular’ vanillin which is present in vanilla.
It is a slightly different molecule.

Ethyl vanillin is often used to substitute a larger amount of Vanillin in a fragrance when a discoloration problem arises, due to the active hydroxyl- or aldehyde-groups of the Vanillin/Ethylvanillin molecules.

As a flavouring agent, ethyl vanillin due to its fragrance potential is used in the production of chocolate.
It is used in the food and beverage industry as a flavouring agent, specifically for the flavouring of foods, chocolates, ice creams, and beverages.

Ethylvanillin is an artificial molecule, it does not appear in nature naturally, whereas vanillin does. It also happens that ethylvanillin is a lot stronger in flavour than vanillin. Therefore, when using ethylvanillin even less of the molecule is required to get the same intensity of vanillin flavour.

Ethyl vanillin is an important food additive and flavouring agent approved by FAO/WHO, has a vanilla odor four times that of vanillin and shows anti-mutagenic activity.
Ethyl vanillin is used as flavoring agent and/or as an additive by the food, cosmetic, or pharmaceutic industries.
Ethyl vanillin possesses antioxidant and anti-inflammatory properties.
The antioxidant activity of ethyl vanillin was much stronger than that of vanillin in the oxidative hemolysis inhibition assay, but was the same as that of vanillin in the ORAC assay.
Oral administration of ethyl vanillin to mice increased the concentration of ethyl vanillic acid, and effectively raised antioxidant activity in the plasma as compared to the effect of vanillin.
The antioxidant activity of ethyl vanillin might be more beneficial than has been thought in daily health practice.
The anti-angiogenic, anti-inflammatory and anti-nociceptive properties of EVA are based on its suppressive effect on the production of nitric oxide possibly via decreasing the reactive oxygen species level.

Ethyl vanillin, also known as bourbonal or ethyl protal, belongs to the class of organic compounds known as hydroxybenzaldehydes.
These are organic aromatic compoundscontaining a benzene ring carrying an aldehyde group and a hydroxyl group.
Ethyl vanillin is a sweet, caramel, and creamy tasting compound.
Based on a literature review asignificant number of articles have been published on Ethyl vanillin.

elongs to the class of organic compounds known as hydroxybenzaldehydes. These are organic aromatic compounds containing a benzene ring carrying an aldehyde group and a hydroxyl group.

Ethyl Vanillin Applications:
As a flavorant, ethylvanillin is about three times as potent as vanillin and is used in the production of chocolate.
The molecule revolutionized both the design and aesthetics of olfactory art; artist Jacques Guerlain added a large quantity of it to a bottle of Jicky perfume, creating the main accord for the perfume house's flagship fragrance, Shalimar (perfume).
This is one of the earliest uses of synthetic molecules that freed scent artists from the limits of natural materials.

Ethyl Vanillin can be used in Food, Beverage, Pharmaceutical, Health & Personal care products, Agriculture/Animal Feed/Poultry.
Ethyl Vanillin is used as flavor in the production of chocolate, foods, sweets, ice cream, drinks and cosmetics.
Ethyl Vanillin is a chemically synthesized flavoring agent related to vanillin or artificial vanilla.
Ethyl Vanillin is three times as strong as artificial vanillin and acts as an imitation vanilla.

It is a white to light yellow needle like crystalline powder that has a similar aroma to vanilla.
Ethyl Vanillin is used in the food and beverage industry as a flavoring agent.
Specifically, it is used in the flavoring of foods, chocolates, ice creams, and beverages.

Ethyl Vanillin Pharmaceutical Applications:
Ethyl vanillin is used as an alternative to vanillin, i.e. as a flavoring agent in foods, beverages, confectionery, and pharmaceuticals.
Ethyl Vanillin 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.

Ethyl Vanillin APPLICATIONs:
This flavour give the sweet Ethyl Vanillin taste which is more intense than Vanillin.
The strength and sweetness is about 3 to 4 times stronger than Vanillin.
This flavour gives more than sweetness strength when compare to Vanillin.
Ethyl Vanillin incorporates delta and gamma lactones which impart creaminess with Dextrose Monohydrate as carrier.
Ethyl Vanillin is particularly good in all bakery products such as biscuits, cookies, cakes, chocolate products, toffees, ice-cream and cereal products.
The recommended dosage is 0.1% for all bakery, chocolate and confectionary products.
The recommended dosage for beverage products such as milk shakes, chocolate drinks, cereal drinks is 0.05% of base weight.

Use & Benefits:
Flavors are very helpful in cosmetics, just like in other categories like bakery, dairy or confectionary.
In cosmetics, they can be used to mask the disagreeable odor from any of the ingredients or to provide a uniform scent to the product.
The fragrance is a factor because of which people may want to use the same product over and over, to get the same effect at the same time and look and feel fresh.
Vanilla also has a soothing property for the skin.
So, when Ethyl Vanillin is applied to mildly irritated skin, Ethyl Vanillin can show a soothing or calming action.
Ethyl Vanillin is used in all kinds of skincare preparations, hair care preparations, makeup related preparations, and toiletries

USES AND APPLICATIONS of Ethyl Vanillin:
Key applications
-Fragrances
-Flavouring agent
-Confectionery
-Pharmaceuticals
-Beverage
-Personal care
-Beauty products

Industries
-Food
-Cosmetics
-Pharma

Ethyl Vanillin in Food Production
Ethyl Vanillin can be used as perfume in food such as in chocolate, candies, biscuits, instant noodles and bread to improve flavor.

Ethyl Vanillin in Beverage
Ethyl Vanillin can be used as flavor enhancer in beverage.

Ethyl Vanillin in Pharmaceutical
Ethyl Vanillin can be used as intermediate in Pharmaceutical.

Ethyl Vanillin in Health and Personal care
Ethyl Vanillin is widely used as Flavoring Agent; Fragrance Ingredient; MASKING; SOOTHING in Cosmetics and personal care products.

Ethyl Vanillin in Agriculture/Animal Feed/Poultry
Ethyl Vanillin can be used as flavor enhance in Agriculture/Animal Feed/Poultry feed.

Preparation of Ethyl Vanillin:
Ethylvanillin is prepared from catechol, beginning with ethylation to give guaethol.
This ether condenses with glyoxylic acid to give the corresponding mandelic acid derivative, which by oxidation and decarboxylation, gives ethylvanillin.

Natural vanilla.
Vanilla is obtained from the pods of a species of tropical orchid, known as Vanillaplanifolia.
It is a climbing plant that needs the support of trees or poles, and under such conditions it grows to 4,5 m.
Its homeland is Central America, but it is mainly grown in Madagascar, Seychelles, Reunion and Tahiti.
In these areas, artificial pollination of flowers is necessary, since there are no special kinds of bees pollinating vanilla in places of uncultivated growth.
The flowers have narrow cups surrounded by thin petals that slowly develop over a period of several months into long narrow pods measuring about 15-23 cm.
To develop a characteristic vanilla flavor, a drying process is needed, similar to that used for cocoa (different versions of this process are used).
The pods are collected in green and soaked in walnut oil for about a month, after which they fully ripen and turn black.

In the process of drying, glycosides, which are the precursors of aromatic substances, decompose into vanillin and glucose, and although vanillin is the main product, other aromatic substances are formed in small amounts. They contribute to the natural aroma of vanilla, which is absent in the synthetic product.

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

Preparation of Ethyl Vanillin:
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.

Reactivity Profile of Ethyl Vanillin
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.

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

Personal Protective Equipment
MINIMUM PROTECTIVE CLOTHING: When working with this chemical, you should wear impervious coveralls, shoe covers and gloves.
RECOMMENDED RESPIRATOR: Where the neat test chemical is weighed and diluted, wear a NIOSH-approved half face respirator equipped with an organic vapor/acid gas cartridge (specific for organic vapors, HCl, acid gas and SO2) with a dust/mist filter.

Product: Ethyl vanillin FPD-2015A-1992
Version: 1
P280, Wear protective gloves/eye protection/face protection.
P305/351/338, IF IN EYES: Rinse cautiously with water for several minutes.
Remove contact lenses, if present and easy to do.
Continue rinsing.
P312, Call a POISON CENTRE or doctor/physician if you feel unwell.
P337/313, If eye irritation persists: Get medical advice/attention.
P501, Dispose of contents/container to approved disposal site, in accordance with local regulations.
Pictograms: None
Other hazards: None

Firefighting measures for Ethylvanillin
Suitable media: Carbon dioxide, Dry chemical, Foam.
Special hazards arising from the substance or mixture
In case of fire, may be liberated: Carbon monoxide, Unidentified organic compounds.
Advice for fire fighters:
In case of insufficient ventilation, wear suitable respiratory equipment.

Personal precautions, protective equipment and emergency procedures:
Avoid inhalation.
Avoid contact with skin and eyes.

Accidental release measures for Ethylvanillin:
Environmental precautions:
Keep away from drains, surface and ground water, and soil.

Methods and material for containment and cleaning up to Ethylvanillin:
Remove ignition sources. Provide adequate ventilation. Avoid excessive inhalation of vapours.
Contain spillage immediately by use of sand or inert powder.
Dispose of according to local regulations.

Precautions for safe handling to Ethylvanillin:
Keep away from heat, sparks, open flames and hot surfaces. - No smoking. Use personal protective equipment as
required. Use in accordance with good manufacturing and industrial hygiene practices. Use in areas with adequate
ventilation Do not eat, drink or smoke when using this product.

Handling and storage for Ethylvanillin:
Conditions for safe storage, including any incompatibilities:
Store in a well-ventilated place.
Keep container tightly closed.
Keep cool.
Ground/bond container and receiving equipment.
Use explosion-proof electrical, ventilating and lighting equipment.
Use only non-sparking tools.
Take precautionary measures against static discharge.
Specific end use(s):
Flavours,Fragrances: Use in accordance with good manufacturing and industrial hygiene practices.

Storage Conditions of Ethyl Vanillin
Should not be stored near powerful oxidizers or in areas of high fire hazard.
They should be kept cool and the containers electrically grounded to avoid sparks.

Frequently Asked Questions about Ethyl Vanillin:

What does Ethyl Vanillin do as an Adulterant?
Ethylvanillin has been used for decades in the food industry, because it is roughly three times as potently flavorful and fragrant as vanillin. Its scent is slightly different from the latter, and just to demonstrate how much it is used, its scent is best described as “vanilla cake icing,” somewhat sweeter than vanilla from its caramel notes. This is because a tremendous number of food products contain this ingredient.

Ethylvanillin does not exist in nature. When it is encountered in a vanilla extract, it does not arise from the fruit of Vanilla planifolia, but has been added later. As such, the extract cannot be considered pure and natural anymore, and its organoleptic properties will be affected.

Is Ethyl Vanillin Dangerous?
Absolutely not. Ethylvanillin is regarded as a very safe molecule to be used in flavors and aromatic compositions, and has been for decades [2]. The only danger there is to alter an otherwise genuine vanilla extract, which is more precious.

The craving for “all-natural” flavors and fragrances in the last years have in fact had dramatic consequences on the vanilla market. Shortages and unpredictable climatic conditions caused the prices of the vanilla extracts to go all over the place [3]. Using artificial vanillin and ethylvanillin of course does not exactly reproduce the aroma of the natural extract, but can in some instances reduce the pressure on the market.

How do we Detect Ethyl Vanillin?
Ethylvanillin is distinct from vanillin on both gas and liquid chromatographic methods, so it can be detected as a single peak with the proper method. When using mass spectrometry, it also features a very unique mass spectrum, which makes it even easier to spot it. The main challenge is to detect relatively low amounts of the compound. Indeed, since it is more potently aromatic than vanillin, only small quantities are sufficient to obtain the desired aroma.

Ethylvanillin is an efficient and accessible artificial flavoring agent, that can conveniently be used in foods with no risk. When an all-natural vanilla is required, it can be fairly well detected by various chromatographic techniques. Think of ethylvanillin the next time you eye that yummy vanilla cake at the grocery store!

Synonyms of Ethyl Vanillin:

3-Ethoxy-4-hydroxybenzaldehyde
ETHYL VANILLIN
Ethylvanillin
121-32-4
Bourbonal
Ethylprotal
Ethavan
Ethovan
Vanirom
Vanilal
Benzaldehyde, 3-ethoxy-4-hydroxy-
Quantrovanil
Vanillal
4-Hydroxy-3-ethoxybenzaldehyde
Ethyl protal
Vanillin, ethyl-
Rhodiarome
Vanirome
2-Ethoxy-4-formylphenol
Protocatechuic aldehyde ethyl ether
Ethylprotocatechuic aldehyde
3-Ethoxyprotocatechualdehyde
MFCD00006944
Vanbeenol
ethyl-vanillin
Ethylprotocatechualdehyde-3-ethyl ether
3-ETHOXY-4-HYDROXY-BENZALDEHYDE
UNII-YC9ST449YJ
NSC 1803
3-ethoxy-4-hydroxy benzaldehyde
Ethyl vanillin (NF)
Ethyl vanillin [NF]
YC9ST449YJ
CHEBI:48408
Protocatechuic aldehyde 3-ethyl ether
NCGC00091583-02
DSSTox_CID_1968
WLN: VHR DQ CO2
DSSTox_RID_76432
DSSTox_GSID_21968
Quantrovanil, Vanillal
3-Ethoxy-4-hydroxybenzaldehyde, 97%
CAS-121-32-4
FEMA No. 2464
CCRIS 1346
HSDB 945
EINECS 204-464-7
BRN 1073761
Aethylvanillin
AI3-00786
Ethyl Vaniilin FCC
Ethyl vanillin, USAN?
Ethyl protocatechualdehyde
ACMC-209a9x
Ethoxy, Hydroxybenzaldehyde
EC 204-464-7
SCHEMBL30247
3ethoxy-4-hydroxybenzaldehyde
MLS002454403
BIDD:ER0329
3-ethoxyl-4-hydroxybenzaldhyde
5-ethoxy-4-hydroxybenzaldehyde
CHEMBL508676
DTXSID5021968
FEMA 2464
3-ethoxy-4-oxidanyl-benzaldehyde
NSC1803
2-ETHOXY-4-FORMYL PHENOL
HMS2267D23
Ethyl vanillin, analytical standard
HY-B0940
NSC-1803
NSC67240
ZINC2567934
Tox21_113535
Tox21_202125
Tox21_302903
3-Ethoxy-4-Hydroxybenzaldehyde,(S)
ANW-17587
BBL023011
NSC-67240
s4568
SBB008268
STK353630
Ethyl vanillin, >=98%, FCC, FG
AKOS000119395
AM84355
CCG-213720
CS-4409
MCULE-6885277569
PS-4030
NCGC00091583-01
NCGC00091583-03
NCGC00091583-04
NCGC00256500-01
NCGC00259674-01
AC-10881
Ethyl proto-catechualdehyde-3-ethyl ether
I915
NCI60_001511
SMR001252229
SY011364
DB-061895
E0050
FT-0615625
ST45162590
D01086
D70878
45191-EP2295424A1
45191-EP2311821A1
45191-EP2374783A1
45191-EP2377841A1
AB00949623_05
A804713
Q416958
SR-01000865052
Q-200375
SR-01000865052-2
3-Ethoxy-4-hydroxybenzaldehyde, ReagentPlus(R), 99%
F2190-0622
3-Ethoxy-4-hydroxybenzaldehyde, Vetec(TM) reagent grade, 99%
Ethyl vanillin, United States Pharmacopeia (USP) Reference Standard
Ethyl vanillin, Pharmaceutical Secondary Standard; Certified Reference Material