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3,3-DIETHOXY-1-PROPANOL

CAS No.
16777-87-0
Chemical Name:
3,3-DIETHOXY-1-PROPANOL
Synonyms
3,3-diethoxypropanol;3,3-DIETHOXY-1-PROPANOL;3,3-Diethoxy-propan-1-ol;1-Propanol, 3,3-diethoxy-;3,3-Diethoxy-1-propanol 98%;3-hydroxypropionaldehyde diethyl acetal
CBNumber:
CB3243815
Molecular Formula:
C7H16O3
Molecular Weight:
148.2
MDL Number:
MFCD00074850
MOL File:
16777-87-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 01:04:22
Product description Number Pack Size Price
3,3-Diethoxy-1-propanol 98% 273252 1g $62.9
3,3-Diethoxy-1-propanol 98% 273252 5g $194
3,3-Diethoxy-1-propanol TRC-D442995-250MG 250mg $65
3,3-Diethoxy-1-propanol TRC-D442995-2.5G 2.5g $334
3,3-Diethoxy-1-propanol TRC-D442995-1G 1g $179
More product size

3,3-DIETHOXY-1-PROPANOL Properties

Boiling point 90-93 °C/14 mmHg (lit.)
Density 0.941 g/mL at 25 °C (lit.)
refractive index n20/D 1.421(lit.)
Flash point 196 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Liquid
pka 15.05±0.10(Predicted)
color Clear colorless
InChI InChI=1S/C7H16O3/c1-3-9-7(5-6-8)10-4-2/h7-8H,3-6H2,1-2H3
InChIKey ASERXEZXVIJBRO-UHFFFAOYSA-N
SMILES C(O)CC(OCC)OCC
LogP 0.789 (est)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H335-H319
Precautionary statements  P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
PPE Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
WGK Germany  3
HS Code  29094980
Storage Class 10 - Combustible liquids

3,3-DIETHOXY-1-PROPANOL price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 273252 3,3-Diethoxy-1-propanol 98% 16777-87-0 1g $62.9 2026-04-30 Buy
Sigma-Aldrich 273252 3,3-Diethoxy-1-propanol 98% 16777-87-0 5g $194 2026-04-30 Buy
TRC TRC-D442995-250MG 3,3-Diethoxy-1-propanol 16777-87-0 250mg $65 2026-06-03 Buy
TRC TRC-D442995-2.5G 3,3-Diethoxy-1-propanol 16777-87-0 2.5g $334 2026-06-03 Buy
TRC TRC-D442995-1G 3,3-Diethoxy-1-propanol 16777-87-0 1g $179 2026-06-03 Buy
Product number Packaging Price Buy
273252 1g $62.9 Buy
273252 5g $194 Buy
TRC-D442995-250MG 250mg $65 Buy
TRC-D442995-2.5G 2.5g $334 Buy
TRC-D442995-1G 1g $179 Buy

3,3-DIETHOXY-1-PROPANOL Chemical Properties,Uses,Production

Uses

3,3-Diethoxy-1-propanol was used in the synthesis of α-acetal-poly(ethylene glycol) via reaction with potassium napthalide and ethylene oxide inside an UniLab Glovebox.

Synthesis

Ethyl 3,3-Diethoxypropionate

10601-80-6

3,3-DIETHOXY-1-PROPANOL

16777-87-0

Tetrahydrofuran (THF) was dehydrated through 4Å molecular sieves overnight and set aside. Under nitrogen protection, 2.2 kg of dehydrated THF was added to a 5 L four-necked flask and cooled to below 10 °C. 50 g of lithium aluminum hydride was slowly added, followed by dropwise addition of 250 g of ethyl 3,3-diethoxypropionate, controlling the internal temperature not to exceed 10 °C. After the dropwise addition was completed, the temperature was raised to 20°C and the reaction was carried out for 1 hour. After completion of the reaction, 420 g of distilled water was added and stirred for 2 h. The filtrate was filtered through No. 2 filter paper and the cake was washed with 1.1 kg of THF. The filtrate was concentrated at 40 °C to give 213 g of crude 3,3-diethoxy-1-propanol (abbreviated as 33DEP). 200g of crude 33DEP was taken in a 5L four-necked flask, 1kg of hexane was added and stirred for 1 hour (Step A). Add 1kg of 0.1M phosphate buffer (pH 7.5), stir for 20 minutes and transfer to a 5L separatory funnel and leave to stratify. After separating the aqueous layer, the hexane layer was returned to the flask and the aqueous layer was recovered by repeating the addition of 1 kg of 0.1 M phosphate buffer (pH 7.5), stirring for 20 minutes, and again transferring to a partitioning funnel for stationary partitioning (Step B). The combined aqueous layer was transferred back to a 5L four-necked flask, 2kg of chloroform was added, stirred for 30 minutes, transferred to a 5L partition funnel and left to stratify for 15 minutes. The chloroform layer was recovered and the aqueous layer was repeated once with 2 kg chloroform extraction and the chloroform layers were combined (Step C). The chloroform layer was concentrated at 40°C and residual solvent was removed by nitrogen bubbling. 20g of 4Å molecular sieve was added and filtered after stirring for 5 h to give 188 g of 33DEP. 150 g of 33DEP was taken in a 300 mL four neck flask and subjected to reduced pressure distillation. The first fraction was collected at 0.4 kPa, bath temperature of 38°C, internal temperature of 36°C, and temperature at the top of the tower of 33°C. Subsequently, the bath temperature was gradually increased, and the main fraction was collected at 0.2 kPa, bath temperature of 58 °C, internal temperature of 55 °C, and temperature of the top of the tower of 54 °C, and the temperature of the top of the tower was controlled not to exceed 60 °C, and finally 138 g of the main fraction was obtained (Step D). The main fraction was analyzed by GC and the results are shown in Table 1.

References

[1] Patent: US2012/277477, 2012, A1. Location in patent: Page/Page column 5
[2] Acta Chemica Scandinavica (1947-1973), 1973, vol. 27, p. 239 - 250
[3] Patent: US4634773, 1987, A

3,3-DIETHOXY-1-PROPANOL Preparation Products And Raw materials

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Aladdin Scientific
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View Lastest Price from 3,3-DIETHOXY-1-PROPANOL manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3,3-DIETHOXY-1-PROPANOL pictures 2026-06-30 3,3-DIETHOXY-1-PROPANOL
16777-87-0
1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
3,3-DIETHOXY-1-PROPANOL pictures 2019-07-06 3,3-DIETHOXY-1-PROPANOL
16777-87-0
$1.00 1KG 98% 1 Career Henan Chemical Co
3,3-DIETHOXY-1-PROPANOL 3,3-diethoxypropanol 3,3-Diethoxy-1-propanol 98% 3,3-Diethoxy-propan-1-ol 1-Propanol, 3,3-diethoxy- 3-hydroxypropionaldehyde diethyl acetal 16777-87-0 C2H5O2CHCH2CH2OH Organic Building Blocks Oxygen Compounds Building Blocks Alcohols C7 to C8 Alcohols C7 to C8 Oxygen Compounds Building Blocks C7 to C8 Chemical Synthesis Organic Building Blocks Oxygen Compounds