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Isovanillin

CAS No.
621-59-0
Chemical Name:
Isovanillin
Synonyms
3-HYDROXY-4-METHOXYBENZALDEHYDE;ISOVANILIN;sovanillin;5-Formylguaiacol;3-Hydroxy-4-methoxy;Benzaldehyde,3-hydroxy-4-methoxy-;NSC 82996;ISOVANILLIN;lsovanillin;AKOS B022473
CBNumber:
CB0705725
Molecular Formula:
C8H8O3
Molecular Weight:
152.15
MDL Number:
MFCD00003369
MOL File:
621-59-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:06
Product description Number Pack Size Price
3-Hydroxy-4-methoxybenzaldehyde 99% 143685 25g $75
3-Hydroxy-4-methoxybenzaldehyde 99% 143685 100g $109
Isovanillin >98.0%(T) H0263 25g $59
Isovanillin >98.0%(T) H0263 250g $251
ISOVANILLIN 95% 28811 5G $10
More product size

Isovanillin Properties

Melting point 113-116 °C
Boiling point 179 °C15 mm Hg(lit.)
Density 1.20
vapor pressure 0Pa at 20℃
refractive index 1.4945 (estimate)
Flash point 179°C/15mm
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Soluble in acetone and methanol.
pka pK1:8.889 (25°C)
form crystalline
color faintly brown
Water Solubility 2.27g/L at 20℃
Sensitive Air Sensitive
BRN 1073021
InChI 1S/C8H8O3/c1-11-8-3-2-6(5-9)4-7(8)10/h2-5,10H,1H3
InChIKey JVTZFYYHCGSXJV-UHFFFAOYSA-N
SMILES COc1ccc(C=O)cc1O
LogP 0.95 at 20℃
CAS DataBase Reference 621-59-0(CAS DataBase Reference)
FDA UNII 4A9N90H9X6
NIST Chemistry Reference Benzaldehyde, 3-hydroxy-4-methoxy-(621-59-0)
EPA Substance Registry System Benzaldehyde, 3-hydroxy-4-methoxy- (621-59-0)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H335-H315-H319
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36/37-36
WGK Germany  3
RTECS  CU6540000
Hazard Note  Irritant
TSCA  TSCA listed
HS Code  29124900
Storage Class 11 - Combustible Solids
NFPA 704
1
2 0

Isovanillin price More Price(53)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 143685 3-Hydroxy-4-methoxybenzaldehyde 99% 621-59-0 25g $75 2026-04-30 Buy
Sigma-Aldrich 143685 3-Hydroxy-4-methoxybenzaldehyde 99% 621-59-0 100g $109 2026-04-30 Buy
TCI Chemical H0263 Isovanillin >98.0%(T) 621-59-0 25g $59 2026-04-30 Buy
TCI Chemical H0263 Isovanillin >98.0%(T) 621-59-0 250g $251 2026-04-30 Buy
AstaTech 28811 ISOVANILLIN 95% 621-59-0 5G $10 2026-04-30 Buy
Product number Packaging Price Buy
143685 25g $75 Buy
143685 100g $109 Buy
H0263 25g $59 Buy
H0263 250g $251 Buy
28811 5G $10 Buy

Isovanillin Chemical Properties,Uses,Production

Chemical Properties

Light Tan Cyrstalline Solid

Uses

3-Hydroxy-4-methoxybenzaldehyde was used as starting reagent during the two-step stereoselective synthesis of the anticancer drug (Z)-combretastatin A-4 and glycitein synthesis.

Application

Isovanillin is a kind of fragrance and isomer of vanillin. it has unique properties than vanillin, its fragrance can change with the change of ambient temperature, so it is especially suitable for special cosmetics and some special fragrance industries. Isovanillin is a selective inhibitor of aldehyde oxidase. It is not a substrate of that enzyme, and is metabolized by aldehyde dehydrogenase into isovanillic acid, which could make it a candidate drug for use in alcohol aversion therapy.

Preparation

Synthesis of isovanillin: 4-Hydroxybenzaldehyde is used as raw material, firstly react with bromine to obtain 3-bromo-4-hydroxybenzaldehyde, then react with methyl iodide to obtain 3-bromo-4-methoxybenzaldehyde, and then hydrolyzed under the action of sodium hydroxide and cuprous chloride to produce isovanillin. The yield was 64.1%.

Definition

ChEBI: Isovanillin is a member of the class of benzaldehydes that is 4-methoxybenzaldehyde substituted by a hydroxy group at position 3. It is an inhibitor of aldehyde oxidase. It has a role as an EC 1.2.3.1 (aldehyde oxidase) inhibitor, a plant metabolite, an antidiarrhoeal drug, an antifungal agent, a HIV protease inhibitor and an animal metabolite. It is a member of phenols, a monomethoxybenzene and a member of benzaldehydes.

Synthesis Reference(s)

The Journal of Organic Chemistry, 45, p. 1596, 1980 DOI: 10.1021/jo01297a010

General Description

3-Hydroxy-4-methoxybenzaldehyde on condensation with furan-2-carboxylic acid hydrazide and thiophene-2-carboxylic acid hydrazide yields Schiff-bases. It undergoes condensation reaction with1-azabicyclo[2.2.2]octan-3-one to give (Z)-2-(3-hydroxy-4-methoxybenzylidene)-1-azabicyclo[2.2.2]octan-3-one.

Flammability and Explosibility

Not classified

target

5-HT Receptor | AChR

Source

Isovanillin is a natural product found in many plant species like Pluchea sagittalis, Pycnocycla spinose, Mondia whitei, Benincasa hispida, Arum Palaestinum, Thalictrum przewalskii, Valeriana officinalis var. latifolia[1].

Purification Methods

Crystallise isovaniline from H2O or *C6H6. The oxime has m 147o. [Beilstein 8 IV 1764.]

References

[1] Ana C. de Carvalho . “Understanding the cytotoxic effects of new isovanillin derivatives through phospholipid Langmuir monolayers.” Bioorganic Chemistry 83 (2019): Pages 205-213.
[2] V. Balachandran , K. Parimala. “Vanillin and isovanillin: Comparative vibrational spectroscopic studies, conformational stability and NLO properties by density functional theory calculations.” Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 95 (2012): Pages 354-368.

1131-52-8
621-59-0
Synthesis of Isovanillin from 3-Ethoxy-4-methoxybenzaldehyde
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4-METHOXY-3-HYDROXYBENZALDEHYDE pictures 2026-03-20 4-METHOXY-3-HYDROXYBENZALDEHYDE
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US $0.00 / mg 10mg 0.98 10g ShenZhen H&D Pharmaceutical Technology Co., LTD
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US $0.10 / KG 0.1KG 99.5% 200TONS Shaanxi Dideu Medichem Co. Ltd
  • Isovanillin pictures
  • Isovanillin
    621-59-0
  • US $0.10 / KG
  • 99.5%
  • Shaanxi Dideu Medichem Co. Ltd
ISOVANILLIN 3-HYDROXY-4-ANISALDEHYDE 3-HYDROXYANISALDEHYDE 3-HYDROXY-P-ANISALDEHYDE AKOS B022473 AKOS BBS-00003278 TIMTEC-BB SBB008245 2-Methoxy-5-formylphenol 4-METHOXY-3-HYDROXYBENZALDEHYDE 3-Hydroxy-4-methoxybenzaldehyd p-Anisaldehyde,3-hydroxy- 3-Hydorxy-4-Methoxy Benzoic Acid 3-Hydroxy-4-methylhoxy benzaldehyde ISOVANILLIN, MATRIX SUBSTANCE FOR MALDI- MS Isovanilllin Isovanillin, 3-Hydroxyanisaldehyde Isovanillin, 3-Hydroxy-p-anisaldehyde, 5-Formylguaiacol, 5-Formyl-2-methoxyphenol 3-Hydroxy-4-Methoxybenzaldehyde, 97+% Extraordinary fragrance LanSu Isovanillin Synonyms 3-Hydroxy-4-methoxybenzaldehyde Isovanillin >=95.0% 3-hydroxy-4-methoxy-benzaldehyd 3-hydroxy-p-anisaldehyd Benzaldehyde,3-hydroxy-4-m 3-HYDROXY-4-METHOXYBENZALDEHYDE / ISOVANILLIN 3-HYDROXY-4-METHOXYBENZALDEHYDE 99+% ISOVANILLIN (3-HYDROXY-4-METHOXYBENZALDEHYDE) NSC 82996 3-Hydroxy-4-methoxybenzaldehyde 4-Methoxy-3-hydroxybenzaldehyde 3-Hydroxy-4-methoxybenzaldehyde, 98+% 3-Hydroxyanisaldehyde, Isovanillin 3-Hydroxy-4-methoxybenzaldehyde, 3-Hydroxyanisaldehyde 3-Hydroxy-para-anisaldehyde 5-Formyl-2-methoxyphenol Isovanicaline Isovanillicaldehyde Isovanilline Oxy-3 methoxy-4 benzaldehyde oxy-3methoxy-4benzaldehyde p-Anisaldehyde, 3-hydroxy- 3-Hydroxy-4-Methoxybenzaldehyde, 98% 5GR 3-Hydroxy-4-methoxybenzaL Isovanillin> 3-Hydroxy-4-methoxybenzaldehyde, 99%, for synthesis Isovanillin,>98% Gefitinib Impurity 42 (Isovanillin) Gefitinib Impurity 91 3-Hydroxy-4-methoxybenzaldehyde USP/EP/BP Entacapone Impurity 79 Bloom Tech Chemical Reagent Isovanillin CAS?621-59-0 ISOVANILINE Extra Pure 11 Dihydrocarbamezer 11-hydroxy-10 ISOVANILIN 3-HYDROXY-4-METHOXYBENZALDEHYDE 3-Hydroxy-4-methoxy 5-Formylguaiacol Benzaldehyde,3-hydroxy-4-methoxy-