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538256

Sigma-Aldrich

2,2-Dimethyl-1,3-propanediol

99%

Synonym(s):

NPG Glycol, Neopentylglycol

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About This Item

Linear Formula:
(CH3)2C(CH2OH)2
CAS Number:
126-30-7
Molecular Weight:
104.15
Beilstein:
605291
EC Number:
204-781-0
MDL number:
MFCD00004685
UNSPSC Code:
12352100
PubChem Substance ID:
24878314
NACRES:
NA.22

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

SMILES string

CC(C)(CO)CO

InChI

1S/C5H12O2/c1-5(2,3-6)4-7/h6-7H,3-4H2,1-2H3

InChI key

SLCVBVWXLSEKPL-UHFFFAOYSA-N

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General description

2,2-Dimethyl-1,3-propanediol readily absorbs moisture on exposure to air.

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)

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

672289

2,2-Dibenzyl-1,3-propanediol

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)
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
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
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