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Safety Information

533734

Sigma-Aldrich

1,3-Propanediol

≥99.6%

Synonym(s):

1,3-Dihydroxypropane, Trimethylene glycol

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About This Item

Linear Formula:
HO(CH2)3OH
CAS Number:
Molecular Weight:
76.09
Beilstein:
969155
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:

vapor pressure

0.8 mmHg ( 20 °C)
9.8 mmHg ( 100 °C)

Assay

≥99.6%

impurities

<0.1% water

refractive index

n20/D 1.440 (lit.)

surface tension

46.2 dyn/cm, 20 °C

viscosity

52 cP(20 °C)(lit.)

bp

214 °C/760 mmHg (lit.)

mp

−27 °C (lit.)

solubility

H2O: soluble

density

1.053 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): <0.5 ppm

SMILES string

OCCCO[H]

InChI

1S/C3H8O2/c4-2-1-3-5/h4-5H,1-3H2

InChI key

YPFDHNVEDLHUCE-UHFFFAOYSA-N

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Application

For applications, see P5040-4

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Celia L Menckeberg et al.
Gut, 64(6), 884-893 (2014-07-25)
Repetitive interaction with microbial stimuli renders epithelial cells (ECs) hyporesponsive to microbial stimulation. Previously, we have reported that buccal ECs from a subset of paediatric patients with Crohn's disease are not hyporesponsive and spontaneously released chemokines. We now aimed to
E Celińska
Biotechnology advances, 28(4), 519-530 (2010-04-07)
The history of 1,3-propanediol (1,3-PD) conversion from being a specialty chemical to being a bulk chemical illustrates that the concerted effort of different metabolic engineering approaches brings the most successful results. In order to metabolically tailor the 1,3-PD production pathway
Sarbjit S Saini et al.
The Journal of investigative dermatology, 135(1), 67-75 (2014-07-22)
ASTERIA I was a 40-week, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of subcutaneous omalizumab as add-on therapy for 24 weeks in patients with chronic idiopathic urticaria/spontaneous urticaria (CIU/CSU) who remained symptomatic despite H1 antihistamine treatment at
R K Saxena et al.
Biotechnology advances, 27(6), 895-913 (2009-08-12)
1,3-Propanediol, a valuable bifunctional molecule, can be produced from renewable resources using microorganisms. It has several promising properties for many synthetic reactions, particularly for polymer and cosmetic industries. By virtue of being a natural product, relevant biochemical pathways can be
Charles E Nakamura et al.
Current opinion in biotechnology, 14(5), 454-459 (2003-10-29)
Improvements in the biological production of 1,3-propanediol, a key component of an emerging polymer business, have been realized. Utilizing genes from natural strains that produce 1,3-propanediol from glycerol, metabolic engineering has enabled the development of a recombinant strain that utilizes

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