P-ANISALDEHYDE DIMETHYL ACETAL

Product Name: P-ANISALDEHYDE DIMETHYL ACETAL
CAS No.: 2186-92-7
Chemical Name: P-ANISALDEHYDE DIMETHYL ACETAL
Synonyms: -4-methoxybenzene;ANISIC ALDEHYDE DMA;1-(Dimethoxymethyl);Nintedanib Impurity 33;α,α,4-Trimethoxytoluene;Anisaldehyddimethylacetal;p-(dimethoxymethyl)anisole;4-(Dimethoxymethyl)anisole;ANISALDEHYDE DIMETHYL ACETAL;Anisicaldehydedimethylacetal
CBNumber: CB7140121
Molecular Formula: C10H14O3
Formula Weight: 182.22
MOL File: 2186-92-7.mol

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P-ANISALDEHYDE DIMETHYL ACETAL Property

Boiling point:: 85-87 °C0.1 mm Hg(lit.)
Density: 1.07 g/mL at 20 °C(lit.)
vapor pressure: 2.407-48Pa at 25-61.2℃
refractive index: n20/D 1.505
Flash point:: 97°C
storage temp.: 2-8°C
solubility: H2O: soluble
form: Liquid
color: Clear colorless to light yellow
Odor: Herbal-green, somewhat floral odor, suggestive of Lilac (“Lilac-green’”), Hyacinth, Appleblossom, etc.
Odor Type: floral
Water Solubility: Miscible with alcohol and many organic solvents. Slightly miscible with water.
BRN: 2048930
LogP: 2 at 25℃
CAS DataBase Reference: 2186-92-7(CAS DataBase Reference)
EPA Substance Registry System: p-(Dimethoxymethyl)anisole (2186-92-7)

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Safety

Safety Statements: 24/25
WGK Germany: 1
F: 10
TSCA: Yes
HS Code: 29110000

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

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

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

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.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 10445
Product name: Anisaldehyde dimethyl acetal
Purity: ≥98.5% (GC)
Packaging: 50mL
Price: $159
Updated: 2025/07/31

TCI Chemical

Product number: A1247
Product name: p-Anisaldehyde Dimethyl Acetal
Purity: >97.0%(GC)
Packaging: 25mL
Price: $49
Updated: 2025/07/31

TCI Chemical

Product number: A1247
Product name: p-Anisaldehyde Dimethyl Acetal
Purity: >97.0%(GC)
Packaging: 500mL
Price: $387
Updated: 2025/07/31

TRC

Product number: A673205
Product name: Anisaldehyde dimethyl acetal
Packaging: 1g
Price: $50
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FA55064
Product name: p-Anisaldehyde dimethyl acetal
Packaging: 250g
Price: $400
Updated: 2021/12/16

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P-ANISALDEHYDE DIMETHYL ACETAL Chemical Properties,Usage,Production

Chemical Properties

clear colorless to light yellow liquid

Uses

4-Methoxybenzaldehyde dimethyl acetal is used as a precursor to 1-methoxy-1-(4-methoxyphenyl)hept-2-yne, 2,5-dioxopyrrolidin-1-yl-3-((4R)-2-(4-methoxyphenyl)-5,5-dimethyl-1,3-dioxane-4-carboxamido)propanoate and 1-(p-anisyl)-2-(2-methoxyethyl)-3-phenylindene. Further, it acts as a protecting group reagent for diols, especially in carbohydrates. It is also used as a flavor essence in sunflower, cyclamen and in jasmine. In addition to this, it is involved in allylation reactions with allyltrimethylsilane catalyzed by Iron(III) chloride.

Synthesis

P-Anisaldehyde diMethyl acetal is produced from Anisaldehyde and Methyl alcohol.

P-ANISALDEHYDE DIMETHYL ACETAL Preparation Products And Raw materials

Raw materials

Preparation Products

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P-ANISALDEHYDE DIMETHYL ACETAL Suppliers

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View Lastest Price from P-ANISALDEHYDE DIMETHYL ACETAL manufacturers

Career Henan Chemical Co

Product: 4-Methoxybenzaldehyde dimethyl acetal 2186-92-7
Price: US $1.00/KG
Min. Order: 1KG
Purity: 98%
Supply Ability: 200kgs
Release date: 2020-01-09

2186-92-7, P-ANISALDEHYDE DIMETHYL ACETALRelated Search:

1,3-DiMethyl 2-[4-(Methoxycarbonyl)-2-nitrophenyl]propanedioate 1-Chloro-4-(trimethoxymethyl)benzene Nintedanib Impurity 76 ALPHA,ALPHA,2,4-TETRACHLOROTOLUENE 1-ACETYL-2-OXO-2,3-DIHYDRO-1H-INDOLE-5-CARBOXYLIC ACID METHYL ESTER 2-OXO-2,3-DIHYDRO-1H-INDOLE-6-CARBOXYLIC ACID ETHYL ESTER N-methyl-2-(4-methylpiperazin-1-yl)-N-(4-nitrophenyl)acetamide (Z)-methyl 3-(((4-(methylamino)phenyl)amino)(phenyl)methylene)-2-oxoindoline-6-carboxylate N-Methyl-4-nitroaniline 2-PROPANESULFONIC ACID SODIUM SALT MON& Nintedanib Impurity 67 Nintedanib Impurity 107 1,2-dichloro-4-(dichloromethyl)benzene BIBF 1202 Nintedanib Impurity 62 Ethanesulfonic acid isopropyl ester Methyl oxindole-5-carboxylate Nintedanib Impurity 52 Anisaldehyde Dimethyl Acetal

1-(dimethoxymethyl)-4-methoxy-benzen

1-(dimethoxymethyl)-4-methoxy-Benzene

P-ANISALDEHYDE DIMETHYL ACETAL

Anisicaldehydedimethylacetal

4-METHOXYBENZALDEHYDE DIMETHYL ACETAL

ANISALDEHYDE DIMETHYL ACETAL

ANISIC ALDEHYDE DMA

p-(dimethoxymethyl)anisole

Benzene, 1-(dimethoxymethyl)-4-methoxy-

Anisaldehyddimethylacetal

4-chlorobenzoic acid [5-chloro-3-[(4-chlorophenyl)-oxomethoxy]-2-oxolanyl]methyl ester

4-Methoxybenzaldehyde dimethyl acetal, 98+%

alpha,alpha,4-Trimethoxytoluene

4-Methoxybenzaldehyde dimethyl acetal, α,α,4-Trimethoxytoluene

1-Methoxy-4-(dimethoxymethyl)benzene

4-(Dimethoxymethyl)anisole

p-Anisaldehyde dimethyl acetal,98%

p-Anisaldehyde Dimethyl Acetalp-Anisaldehyde Dimethyl Acetal

α,α,4-Trimethoxytoluene

p-Anisaldehyde diethyl acetal

p-Anisaldehyde diMethyl acetal, 98% 25GR

4-Methoxybenzaldehyde Dimethyl Acetal alpha,alpha,4-Trimethoxytoluene

AnisaldehydediMethyl acetaltwo

Anisaldehyde dimethyl acetal >=98.5% (GC)

1-(Dimethoxymethyl)

-4-methoxybenzene

Nintedanib Impurity 33

4-Methoxybenzaldehyde dimethyl acetal (Anisaldehyde dimethyl acetal)

p-Anisaldehyde Dimethyl Acetal &gt

para-anisaldehyde dimethyl acetal

p-Methoxybenzaldehyde dimethylacetal

(E)-methyl 3-(((4-(2-(4-(tert-butoxycarbonyl)piperazin-1-yl)-N-methylacetamido)phenyl)amino)(phenyl)methylene)-2-oxoindoline-6-carboxylate

Anisaldehyde dimethyl acetal, 97%

2186-92-7

33402-03-9

Building Blocks

Reagents for Oligosaccharide Synthesis

Organic Building Blocks

Acetals/Ketals/Ortho Esters

Oxygen Compounds

Biochemistry

Reagents for Oligosaccharide Synthesis