219800
2-Hydroxyhexanoic acid
98%
Synonym(s):
DL-α-Hydroxycaproic acid
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About This Item
Linear Formula:
CH3(CH2)3CH(OH)CO2H
CAS Number:
Molecular Weight:
132.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
mp
60-62 °C (lit.)
functional group
carboxylic acid
hydroxyl
SMILES string
CCCCC(O)C(O)=O
InChI
1S/C6H12O3/c1-2-3-4-5(7)6(8)9/h5,7H,2-4H2,1H3,(H,8,9)
InChI key
NYHNVHGFPZAZGA-UHFFFAOYSA-N
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General description
Solubility of 2-hydroxyhexanoic acid in supercritical CO2 has been studied.
Application
2-Hydroxyhexanoic acid was used in the synthesis of aliphatic copolyesters.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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K J Ng et al.
Journal of chromatography, 228, 43-50 (1982-03-12)
Amniotic fluid from different gestational age patients was partitioned into neutral, acidic and basic fractions. The organic acids were trimethylsilylated and analyzed by glass capillary gas chromatography-mass spectrometry. A marked difference in the level of hippuric acid was observed between
Grazyna Adamus et al.
Rapid communications in mass spectrometry : RCM, 18(13), 1436-1446 (2004-06-25)
A series of aliphatic copolyesters was obtained from (R,S)-beta-butyrolactone and two isomeric hydroxy acids, 6-hydroxyhexanoic and (R,S)-2-hydroxyhexanoic acids. The reactions were conducted in bulk without catalyst. Electrospray ionization tandem mass spectrometry (ESI-MSn) was used for molecular characterization of these copolyester
J B Brooks et al.
Journal of clinical microbiology, 25(2), 445-448 (1987-02-01)
Serum (SR) and cerebrospinal fluid (CSF) from a patient suspected of having tuberculous meningitis were submitted to our laboratory for analysis by frequency-pulsed electron capture gas-liquid chromatography (FPEC GLC). The samples were tested for the presence of carboxylic acids, alcohols
L I Woolf et al.
Journal of chromatography, 231(2), 237-245 (1982-09-10)
Plasma or whole blood is treated with o-phenylenediamine dihydrochloride in phosphoric acid under conditions found spectrophotometrically to give maximum yields of the quinoxalinols. The quinoxalinols are extracted and, after removing phosphoric acid, etc., silylated with bis-trimethylsilyltrifluoracetamide in acetonitrile. Other solvents
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The branched-chain amino acid (BCAA) related 2-hydroxy carboxylic acid isoleucic acid (ILA) enhances salicylic acid-mediated pathogen defense in Arabidopsis thaliana. ILA has been identified in A. thaliana as its glucose conjugate correlated with the activity of the small-molecule glucosyltransferase UGT76B1
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