Benzaldehyde dimethyl acetal
Benzaldehyde Dimethylacetal
CAS: 1125-88-8
Molecular Formula: C9H12O2
Benzaldehyde dimethyl acetal - Names and Identifiers
| Name | Benzaldehyde Dimethylacetal |
| Synonyms | Intedanib Impurity 8 (dimethoxymethyl)benzene (dimethoxymethyl)-benzen Benzaldehde diMethyl acetal Benzaldehyde Dimethylacetal Benzaldehyde dimethyl acetal 2-(1-Methoxyethoxy)benzaldehyde BENZALDEHYDE DIMETHYL ACETAL FOR SYNTHES |
| CAS | 1125-88-8 |
| EINECS | 214-413-0 |
| InChI | InChI=1/C9H12O2/c1-10-9(11-2)8-6-4-3-5-7-8/h3-7,9H,1-2H3 |
| InChIKey | HEVMDQBCAHEHDY-UHFFFAOYSA-N |
Benzaldehyde dimethyl acetal - Physico-chemical Properties
| Molecular Formula | C9H12O2 |
| Molar Mass | 152.19 |
| Density | 1.014 g/mL at 25 °C (lit.) |
| Melting Point | 87-89 C |
| Boling Point | 87-89 °C/18 mmHg (lit.) |
| Flash Point | 157°F |
| JECFA Number | 837 |
| Water Solubility | decomposes |
| Vapor Presure | 0.476mmHg at 25°C |
| Appearance | Colorless liquid |
| Color | Clear colorless |
| BRN | 2044501 |
| Storage Condition | Inert atmosphere,2-8°C |
| Sensitive | Moisture Sensitive |
| Refractive Index | n20/D 1.493(lit.) |
| MDL | MFCD00008491 |
| Use | This product is for scientific research only and shall not be used for other purposes. |
Benzaldehyde dimethyl acetal - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R22 - Harmful if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S23 - Do not breathe vapour. S24/25 - Avoid contact with skin and eyes. |
| RTECS | CU5774000 |
| FLUKA BRAND F CODES | 10-21 |
| TSCA | Yes |
| HS Code | 29110000 |
| Hazard Class | IRRITANT |
| Toxicity | LD50 orally in Rabbit: 1220 mg/kg LD50 dermal Rabbit > 5000 mg/kg |
Benzaldehyde dimethyl acetal - Nature
Open Data Verified Data
colorless liquid. It has a fragrance similar to almond. Found in potatoes. Under acidic conditions, it is easy to hydrolyze to generate benzaldehyde, but it is not affected by alkaline environment. It is stable to oxidant or reducing agent, and the stability is better than that of benzaldehyde.
Last Update：2024-01-02 23:10:35
Benzaldehyde dimethyl acetal - Preparation Method
Open Data Verified Data
an acetal is obtained from dehydration and condensation of benzaldehyde with methanol by aldol in the presence of an acid catalyst.
Last Update：2022-01-01 10:08:22
Benzaldehyde dimethyl acetal - Introduction
It is found in potatoes. Benzaldehyde is easily hydrolyzed under acidic conditions, but it is not affected by alkaline environment. It is stable to oxidants or reducing agents, so it is an important form of preserving benzaldehyde (benzaldehyde is easily oxidized by air, if made into acetal, it is easy to preserve).
Last Update：2022-10-16 17:12:17
Benzaldehyde dimethyl acetal - Use
Open Data Verified Data
raw materials of edible flavor and daily flavor. The amount of flavor-based alcoholic beverage is 60mg/kg; The general consumption final amount is 22-56mg/kg.
Last Update：2022-01-01 10:08:22
Benzaldehyde dimethyl acetal - Safety
Open Data Verified Data
The acute oral LD50 of rats was 0.83-1. 79g/kg. Rabbit percutaneous LD50 >5g/kg. The product was applied to the skin of rabbits for 1 day under closed conditions to produce slight irritation. No irritation was found after two days in the human closed skin contact test with 4% Vaseline formulation.
Last Update：2022-01-01 10:08:23
Benzaldehyde dimethyl acetal - Reference Information
| FEMA | 2128 | BENZALDEHYDE DIMETHYL ACETAL |
| NIST chemical information | Information provided by: webbook.nist.gov (external link) |
| EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
| Use | Benzaldehyde dimethanol is a liquid with a similar almond fragrance and exists in potato species. It is easy to hydrolyze to generate benzaldehyde under acidic conditions, but it is not affected by alkaline environment. It is an important form of benzaldehyde to preserve the temperature of oxidant or reducing agent. Benzaldehyde dimethanol can be used as a raw material for edible flavors and daily chemical flavors, and can also be used as a reagent for the synthesis of selenium carbonyl compounds. Reagents for the synthesis of selenocarbonyl compounds An effective reagent for constructing selenocarbonyl compounds |
| Preparation | Benzaldehyde dimethanol can be prepared by the dehydration condensation reaction of benzaldehyde and methanol. For spices, it can be used as a green fragrance-floral fragrance component based on lily of the valley or daffodil fragrance, which can have a unique effect. |
| toxicity | LD50 orally in Rabbit: 1220 mg/kg LD50 dermal Rabbit > 5000 mg/kg |
| use limit | limit (FDA,§ 172.515,2001). FEMA(mg/kg): alcohol-free beverage 26; Cold drink 22; Candy 56; Baked products 45; Pudding and gel 50; Alcohol-containing beverage 60. |
Last Update：2024-04-09 20:52:54
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View History
Benzaldehyde dimethyl acetal
5-[[4-[[2-(Sodiooxycarbonyl)ethyl]carbamoyl]phenyl]azo]-2-hydroxybenzoic acid sodium salt
2-(Difluoromethyl)cyclopropanecarboxylic Acid
2-(3-CHLOROPHENYL)-6-NITROBENZO[D]OXAZOLE
2-methyl-N-(4-{[(4-methyl-2-pyrimidinyl)amino]sulfonyl}phenyl)propanamide
5-[[4-[[2-(Sodiooxycarbonyl)ethyl]carbamoyl]phenyl]azo]-2-hydroxybenzoic acid sodium salt
2-(Difluoromethyl)cyclopropanecarboxylic Acid
2-(3-CHLOROPHENYL)-6-NITROBENZO[D]OXAZOLE
2-methyl-N-(4-{[(4-methyl-2-pyrimidinyl)amino]sulfonyl}phenyl)propanamide