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Home > Product > Material & Chemicals > Polymer/Macromolecule > 3,3-Dimethyl-1,2-butanediol

3,3-Dimethyl-1,2-butanediol | CAS Number: 59562-82-2

Catalog Number
ACM59562822
Product Name
3,3-Dimethyl-1,2-butanediol
Structure
CAS Number
59562-82-2
EC Number
261-805-2
IUPAC Name
3,3-dimethylbutane-1,2-diol
Synonyms
3,3-DIMETHYL-1,2-BUTANEDIOL;3,3-dimethylbutane-1,2-diol;3,3-DIMETHYL-1,2-BUTANEDIOL, TECH., 85+%;3,3-Dimethyl-1,2-butanediol, GC 85%;3,3-DIMETHYL-1,2-BUTANEDIOL: TECH., 90%;3,3-DIMETHYL-1,2-BUTANEDIOL 88%;1-tert-Butyl-1,2-ethanediol;3,3-Dimethyl-1,2-butan
Molecular Weight
118.17
Exact Mass
118.09900
Molecular Formula
C6H14O2
Boiling Point
201-202ºC
Melting Point
37-39ºC
Flash Point
98ºC
Density
0.96g/cm3
Purity
96%
SMILES
CC(C)(C)C(CO)O
InChIKey
YVHAOWGRHCPODY-UHFFFAOYSA-N
H-Bond Donor
2
H-Bond Acceptor
2
Safty Description
24/25
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1Aliphatic and alicyclic diols induce melanogenesis in cultured cells and guinea pig skin.

Brown DA1, Ren WY, Khorlin A, Lesiak K, Conklin D, Watanabe KA, Seidman MM, George J.

J Invest Dermatol. 1998 Apr;110(4):428-37.

We have found that several aliphatic and alicyclic diols induce melanogenesis in cultured S91 mouse melanoma cells and normal human epidermal melanocytes (NHEM). In addition, these compounds induce melanogenesis when applied to guinea pig skin, with transfer of melanin to keratinocytes and formation of "supranuclear caps," as occurs in naturally pigmented skin. The relative order of potency of some of these diols in NHEM is 5-norbornene-2,2-dimethanol > 3,3-dimethyl-1,2-butanediol > cis-1,2-cyclopentanediol > 2,3-dimethyl-2,3-butanediol > 1,2-propanediol. Read More

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