538256
2,2-Dimethyl-1,3-propanediol
99%
Synonym(s):
NPG Glycol, Neopentylglycol
Sign In to View Organizational & Contract Pricing.
Select a Size
All Photos(2)
About This Item
Linear Formula:
(CH3)2C(CH2OH)2
CAS Number:
Molecular Weight:
104.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-781-0
Beilstein/REAXYS Number:
605291
MDL number:
Product Name
2,2-Dimethyl-1,3-propanediol, 99%
InChI key
SLCVBVWXLSEKPL-UHFFFAOYSA-N
InChI
1S/C5H12O2/c1-5(2,3-6)4-7/h6-7H,3-4H2,1-2H3
SMILES string
CC(C)(CO)CO
vapor density
3.6 (vs air)
vapor pressure
<0.8 mmHg ( 20 °C)
assay
99%
autoignition temp.
750 °F
expl. lim.
1.34 %, 149 °F
18.8 %, 177 °F
functional group
hydroxyl
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
2,2-Dimethyl-1,3-propanediol may be used in the synthesis of:
- 2,2-dimethyl-1,3-propanediol cyclic phosphorochloridate
- 2,2-dimethyl-1,3-propanediol cyclic phenylphosphonate
- [1′,3′-(2′,2′-dimethylpropylene)]-2-iodo-3-octyl-5-thienylboronate
- cyclic carbonate
- 2,2-dimethyl-1,3-propanediol bis(cyclic-2,2-dimethyltrimethylene phosphite)
General description
2,2-Dimethyl-1,3-propanediol readily absorbs moisture on exposure to air.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Kallol Gupta et al.
Nature, 541(7637), 421-424 (2017-01-13)
Oligomerization of membrane proteins in response to lipid binding has a critical role in many cell-signalling pathways but is often difficult to define or predict. Here we report the development of a mass spectrometry platform to determine simultaneously the presence
Synthesis of 6-membered cyclic carbonates from 1, 3-diols and low CO2 pressure: a novel mild strategy to replace phosgene reagents
Gregory GL, et al.
Royal Society of Chemistry Advances, 5.49 , 39404-39408 (2015)
New convenient synthesis of highly regioregular poly (3-octylthiophene) based on the Suzuki coupling reaction
Guillerez S and Bidan G
Synt. Metals, 93.2, 123-126 (1998)
Phosphorus-containing derivatives of 2, 2-dimethyl-1, 3-propanediol
McCONNELL RL and Coover Jr HW
The Journal of Organic Chemistry, 24.5, 630-635 (1959)
Sophie Leclercq et al.
Scientific reports, 7, 43306-43306 (2017-02-25)
Bacteria utilize specialized multi-protein machineries to synthesize the essential peptidoglycan (PG) cell wall during growth and division. The divisome controls septal PG synthesis and separation of daughter cells. In E. coli, the lipid II transporter candidate FtsW is thought to
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service