3-aminopropane diol

2,3-dihydroxy-1-propylamine

CAS: 616-30-8 C3 H9 N O2 MW: 91.11013000

Identification

Name3-aminopropane diol
CAS Number616-30-8
EINECS210-475-8
FDA UNIIRH369P864X
Molecular FormulaC3 H9 N O2
Molecular Weight91.11013000
MDL NumberMFCD00008140
Nikkaji NumberJ1.661F
Beilstein1719121

Regulatory

FDA Mainterm (IAUFC)616-30-8 ; 3-AMINO-1,2-PROPANEDIOL
FDA RegulationFDA PART 175 -- INDIRECT FOOD ADDITIVES: ADHESIVES AND COMPONENTS OF COATINGS

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 1.17500 @ 25.00 °C.
Boiling Point 266.00 to 267.00 °C. @ 760.00 mm Hg (est), 264.00 to 266.00 °C. @ 739.00 mm Hg
Vapor Pressure 0.001000 mmHg @ 25.00 °C. (est)
Flash Point > 230.00 °F. TCC ( > 110.00 °C. )
logP (o/w) -2.079 (est)
Soluble in water, 1e+006 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesbuffering agents

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityoral-rat LD50 7500 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorypreparation of polyurethane resins
Recommendation for 3-aminopropane diol usage levels up tonot for fragrance use.
Recommendation for 3-aminopropane diol flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

3- amino-1,2-proopanediol (±)-3- amino-1,2-propandiol (±)-3- amino-1,2-propane diol (±)-3- amino-1,2-propanediol 3- aminopropan-1,2-diol 3- aminopropane-1,2-diol 3- aminopropanediol 2,3- dihydroxy-1-propylamine 2,3- dihydroxypropylamine 2,3- propandiol-1-amine 1,2- propanediol, 3-amino- PubMed: A new bacterial sphingophospholipid containing 3-aminopropane-1,2-diol. PubMed: Chiral 2-endo-substituted 9-oxabispidines: novel ligands for enantioselective copper(II)-catalyzed Henry reactions. PubMed: Self-assembled monolayers with latent aldehydes for protein immobilization. PubMed: Synthesis of 2-Oxo amide triacylglycerol analogues and study of their inhibition effect on pancreatic and gastric lipases.