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ChemicalBook >> CAS DataBase List >>(R)-(+)-Propylene carbonate

(R)-(+)-Propylene carbonate

CAS No.
16606-55-6
Chemical Name:
(R)-(+)-Propylene carbonate
Synonyms
R-Prpylene Carbonate;(R)-PROPYLENE CARBONATE;(R)-Propandiolcarbonate;(R)-PropyleneCarbonate>(R)-(+)-PROPYLENE CARBONATE;(R)-1,2-PROPYLENE CARBONATE;(R)-1,2-PROPANEDIOL CARBONATE;(R)-Propylene Carbonate,99%e.e.;(R)-(+)-1,2-PROPYLENE CARBONATE;(R)-5-Methyl-1,3-dioxolan-2-one
CBNumber:
CB3783423
Molecular Formula:
C4H6O3
Molecular Weight:
102.09
MDL Number:
MFCD00798265
MOL File:
16606-55-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:02:40
Product description Number Pack Size Price
(R)-(+)-Propylene carbonate 98% 540013 5g $81.1
(R)-Propylene Carbonate >98.0%(GC) P1485 5g $42
(R)-Propylene Carbonate >98.0%(GC) P1485 25g $205
(R)-1,2-Propylene Carbonate P9052-55M 100mg $403
(R)-1,2-Propylene carbonate 287102 5g $312
More product size

(R)-(+)-Propylene carbonate Properties

Boiling point 240 °C(lit.)
Density 1.189 g/mL at 25 °C(lit.)
vapor pressure 0.59 psi ( 20 °C)
refractive index n20/D 1.422(lit.)
Flash point >230 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Chloroform (Sparingly)
form Oil
color Clear Colourless to Pale Yellow
Specific Gravity 1.189
optical activity [α]20/D +2°, neat
Water Solubility 175 g/L (25 ºC)
InChI InChI=1S/C4H6O3/c1-3-2-6-4(5)7-3/h3H,2H2,1H3/t3-/m1/s1
InChIKey RUOJZAUFBMNUDX-GSVOUGTGSA-N
SMILES O1C[C@@H](C)OC1=O
CAS DataBase Reference 16606-55-6(CAS DataBase Reference)
UNSPSC Code 12352005
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  FF9650000
HS Code  29329990
REACH Registrations Inactive
NFPA 704
1
0 0

(R)-(+)-Propylene carbonate price More Price(51)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 540013 (R)-(+)-Propylene carbonate 98% 16606-55-6 5g $81.1 2026-04-30 Buy
TCI Chemical P1485 (R)-Propylene Carbonate >98.0%(GC) 16606-55-6 5g $42 2026-04-30 Buy
TCI Chemical P1485 (R)-Propylene Carbonate >98.0%(GC) 16606-55-6 25g $205 2026-04-30 Buy
Usbiological P9052-55M (R)-1,2-Propylene Carbonate 100mg $403 2026-06-04 Buy
Usbiological 287102 (R)-1,2-Propylene carbonate 16606-55-6 5g $312 2026-06-03 Buy
Product number Packaging Price Buy
540013 5g $81.1 Buy
P1485 5g $42 Buy
P1485 25g $205 Buy
P9052-55M 100mg $403 Buy
287102 5g $312 Buy

(R)-(+)-Propylene carbonate Chemical Properties,Uses,Production

Description

(R)-(+)-Propylene carbonate, also known as (R)-1,2-Propanediol cyclic carbonate, presents as a colorless to pale yellow liquid. This compound should keep the container tightly closed and stored in a cool and dark place. For best results, store under inert gas, protected from moisture, as this substance is moisture-sensitive. (R)-(+)-Propylene carbonate is incompatible with oxidizing agents and acids. This chemical causes skin irritation as well as serious eye irritation.

Chemical Properties

Colorless to light yellow liqui

Uses

(R)-1,2-Propylene Carbonate (cas# 16606-55-6) is a compound useful in organic synthesis.

Synthesis

(R)-(-)-1,2-Propanediol

4254-14-2

Diethyl carbonate

105-58-8

(R)-(+)-Propylene carbonate

16606-55-6

The general procedure for the synthesis of R-propylene carbonate from (R)-1,2-propanediol and diethyl carbonate was as follows: (R)-1,2-propanediol (38.05 kg, 500 mol) was added to a glass-lined reactor, followed by the addition of diethyl carbonate (70.88 kg, 600 mol) and sodium ethoxide (3.4 kg, 50 mol). The reaction mixture was heated to 105-110 °C and maintained for 8 hours. After completion of the reaction, unreacted diethyl carbonate was removed by distillation under reduced pressure. After the reaction mixture was cooled to room temperature, the insoluble material was removed by filtration. Finally, the solvent was removed by evaporation of the filtrate to afford R-propylene carbonate (34.24 kg, purity ≥99%) in 90% yield.

References

[1] Patent: CN105859781, 2016, A. Location in patent: Paragraph 0011-0012
[2] Patent: US2010/216822, 2010, A1. Location in patent: Page/Page column 13
[3] Tetrahedron Letters, 1998, vol. 39, # 14, p. 1853 - 1856
[4] Patent: EP1243590, 2002, A2. Location in patent: Page 9
[5] Patent: CN102977146, 2016, B. Location in patent: Paragraph 0016; 0021; 0023

4254-14-2
105-58-8
16606-55-6
Synthesis of (R)-(+)-Propylene carbonate from (R)-(-)-1,2-Propanediol and Diethyl carbonate
Global( 409)Suppliers
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View Lastest Price from (R)-(+)-Propylene carbonate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(R)-(+)-Propylene carbonate pictures 2026-03-30 (R)-(+)-Propylene carbonate
16606-55-6
1KG 99% 20000 Shenzhen Nexcon Pharmatechs Ltd.
(R)-(+)-Propylene carbonate pictures 2026-03-20 (R)-(+)-Propylene carbonate
16606-55-6
$10.00 1KG 99% 100 mt Hebei Chuanghai Biotechnology Co., Ltd
(R)-(+)-Propylene carbonate pictures 2025-12-01 (R)-(+)-Propylene carbonate
16606-55-6
1KG 99.0% 10000KGS Shaanxi Dideu New Materials Co. Ltd
(R)-1,2-PROPANEDIOL CARBONATE (R)-(+)-1,2-PROPYLENE CARBONATE (R)-1,2-PROPYLENE CARBONATE (R)-(+)-PROPYLENE CARBONATE (R)-Propylene Carbonate,99%e.e. (R)-PROPYLENE CARBONATE R-5-Methoxymethyl-2-oxazolidinone (R)-(+)-PROPYLENE CARBONATE, 98% (98% EE (R-(+-PropyleneCarbonate))-IntermediateForTenofovir (r)-1,2-propanediol cyclic carbonate (4R)-4-Methyl-1,3-dioxolan-2-one (R)-1,2-Propanediol cyclic carbonate, (R)-(+)-Propylene carbonate (R)-Propylene carbonate (R)-1,2-Propanediol carbonate (R)-Propandiolcarbonate 1,3-Dioxolan-2-one,4-methyl-,(4R)- (R)-5-Methyl-1,3-dioxolan-2-one Carbonic acid (R)-propylene ester (R)-(+)-Propylene carbonate,98+% (R)-(+)-PROPYLENE CARBONATE, 98% E.E. 98% ASSAY (R)-(+)-Propylene carbonate 98% Tenofovirdisoproxil Impurity 38 (R)-PropyleneCarbonate> (R)-(+)-Propylene carbonate ISO 9001:2015 REACH R-Prpylene Carbonate Tenofovir disoproxil Impurity 92 (R)-(+)-Propylene carbonate 16606-55-6 16606-5-6 6606-55-6 1660-55-6 C5H7O6 Organic Building Blocks Dioxolanes Dioxanes & Dioxolanes Chiral Building Blocks Glycidyl Compounds, etc. (Chiral) Carbonates Asymmetric Synthesis Chiral Compound chiral Chiral Compounds Diols Chiral Reagents Chiral Building Blocks Dioxanes & Dioxolanes Dioxolanes Glycidyl Compounds, etc. (Chiral) Synthetic Organic Chemistry john's
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