ChemicalBook > CAS DataBase List > Isovanillin

Isovanillin

Product Name
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
Formula Weight
152.15
MOL File
621-59-0.mol
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Isovanillin Property

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
InChIKey
JVTZFYYHCGSXJV-UHFFFAOYSA-N
LogP
0.95 at 20℃
CAS DataBase Reference
621-59-0(CAS DataBase Reference)
NIST Chemistry Reference
Benzaldehyde, 3-hydroxy-4-methoxy-(621-59-0)
EPA Substance Registry System
Benzaldehyde, 3-hydroxy-4-methoxy- (621-59-0)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37-36
WGK Germany 
3
RTECS 
CU6540000
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29124900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
143685
Product name
3-Hydroxy-4-methoxybenzaldehyde
Purity
99%
Packaging
25g
Price
$68.3
Updated
2024/03/01
Sigma-Aldrich
Product number
143685
Product name
3-Hydroxy-4-methoxybenzaldehyde
Purity
99%
Packaging
100g
Price
$99
Updated
2024/03/01
TCI Chemical
Product number
H0263
Product name
Isovanillin
Purity
>98.0%(T)
Packaging
25g
Price
$59
Updated
2024/03/01
TCI Chemical
Product number
H0263
Product name
Isovanillin
Purity
>98.0%(T)
Packaging
250g
Price
$251
Updated
2024/03/01
Alfa Aesar
Product number
A12866
Product name
3-Hydroxy-4-methoxybenzaldehyde, 98%
Packaging
5g
Price
$17.65
Updated
2024/03/01
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Isovanillin Chemical Properties,Usage,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.

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Isovanillin Suppliers

Shanghai Kuncheng Industrial Co., LTD
Tel
15317029879
Email
shkcsy@yeah.net
Country
China
ProdList
10
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58
Conier Chem & Pharma Co.,Ltd,
Tel
023-62879767 13996269627;
Fax
+86-28-84559521
Email
sales@conier.com
Country
China
ProdList
294
Advantage
56
Zhongxiang Yaowei Biological Technology Co., Ltd.
Tel
15337241005 13260682861
Email
w13260682861@qq.com
Country
China
ProdList
2435
Advantage
58
JOYCHINE BIO-TECH
Tel
18680818008
Email
18680818008@163.com
Country
China
ProdList
36
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58
Chongqing Yuzhiquan Biological Technology Co., Ltd.
Tel
18306022109
Fax
QQ:2966918840
Email
3236923470@qq.com
Country
China
ProdList
296
Advantage
58
Chongqing Ensky Pharmaceutical Co.,Ltd.
Tel
023-86815286 13983794297
Fax
+86-23-86815116
Email
sales@ensky-chemical.com
Country
China
ProdList
90
Advantage
58
ShenZhen H&D Pharmaceutical Technology Co., LTD
Tel
13217415044
Email
2881949741@qq.com
Country
China
ProdList
4989
Advantage
58
Nanjing Bermuda Biotechnology Co., Ltd.
Tel
027-1734052141618086404407 17340521416
Fax
17340521416
Email
1757224788@qq.com
Country
China
ProdList
2010
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
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View Lastest Price from Isovanillin manufacturers

Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Isovanillin 621-59-0
Price
US $50.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
5000kg/week
Release date
2024-04-24
Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
3-Hydroxy-p-anisaldehyde 621-59-0
Price
US $30.00/kg
Min. Order
1kg
Purity
99
Supply Ability
5000
Release date
2024-04-24
Hebei Weibang Biotechnology Co., Ltd
Product
4-METHOXY-3-HYDROXYBENZALDEHYDE 621-59-0
Price
US $1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
10 mt
Release date
2024-11-01

621-59-0, IsovanillinRelated Search:


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