 |
Did Good |
Sodium Lauryl Sulfate
ToxNet Abstract
ABSTRACT:Final report on the safety assessment of sodium lauryl sulfate and ammonium lauryl sulfate
The following information was generated from the
Toxicology Bibliographic Information (TOXLINE),
a database of the National Library of Medicine's TOXNET system
(http://toxnet.nlm.nih.gov) on March 7, 2006.
Query: The chemical name sodium lauryl sulfate was identified.
The following terms were added from ChemIDplus:
stepanol me
solsol needles
sipon wd
sipon pd
sipex op
neutrazyme
maprofix wac
maprofix neu
irium
duponol waqe
duponol waq
duponol wa
duponol me
duponol c
dreft
carsonol sls
aquarex methyl
aquarex me
CAS Registry Number: 151-21-3
2
TITLE:
Final report on the safety assessment of sodium lauryl sulfate and
ammonium lauryl sulfate
AUTHORS:
Anonymous
SOURCE:
J Am Coll Toxicol Vol:2, 7 (1983) pp 127-81
ABSTRACT:
Sodium and ammonium lauryl sulfate are surfactants used in cosmetics as
cleansing agents. In absorption, metabolism, and excretion studies, sodium
lauryl sulfate had a degenerative effect on the cell membranes because of
its protein denaturing properties. Low levels of skin penetration may
occur at high use concentration. Sodium lauryl sulfate had an LD50 of 0.8
to 1.10 g/kg in rats. A formulation containing 15% ammonium lauryl sulfate
caused depression, labored breathing, diarrhea, and death in four out of
20 animals. In acute ocular tests, 10% sodium lauryl sulfate caused
corneal damage to the rabbits'eyes if not irrigated, or if irrigation was
delayed. A Draize test of a product containing 5.1% sodium lauryl sulfate
caused mild irritation, and products containing 21% detergent were
severely irritating with no rinse, and mildly irritating when rinsed.
Ammonium lauryl sulfate solutions containing 1.25%-27.4% detergent showed
increasing irritation with increasing concentration; rinsing decreased
irritation. Acute animal skin irritation studies of 0.5%-10% sodium lauryl
sulfate caused slight to moderate irritation. Applications of 10%-30%
detergent caused skin corrosion and severe irritation. Solutions of 2%,
10%, and 20% ammonium lauryl sulfate were highly irritating and dangerous.
One percent and 5% sodium lauryl sulfate produced a significant number of
comedones when applied to the pinna of albino rabbits. A chronic oral
feeding study in rats of 0.25%, 0.5%, and 1.0% sodium lauryl sulfate in
the diet for two years produced no abnormalities. A 91-day percutaneous
toxicity study of a shampoo containing 17.5% ammonium lauryl sulfate had
no treatment-related abnormalities except for moderate to severe dermal
effects. In mutagenesis studies, rats fed 1.13% and 0.56% sodium lauryl
sulfate in the diet for 90 days produced no more chromosomal aberrations
or clastogenic effects than did a control diet. Sodium lauryl sulfate was
tested for human skin irritation in concentrations ranging from 0.1% to
10%. Open patches were less irritating than closed patches, and irritation
increased directly with concentration. Similar results were obtained when
formulations containing sodium and ammonium lauryl sulfate were tested. No
UV light sensitization occurred from any formulation in this latter study.
Both sodium and ammonium lauryl sulfate appear to be safe in formulations
designed for discontinuous, brief use followed by thorough rinsing from
the surface of the skin. In products intended for prolonged contact with
skin, concentrations should not exceed 1%.
KEYWORDS:
< ANIMAL >
< HUMAN >
Case report
irritancy
toxicokinetics
genetic toxicity
Teratogens
Cosmetics
Skin
Eye
reproductive effect
dose effect
reproductive and developmental tests
CAS REGISTRY NUMBERS:
151-21-3
2235-54-3
ENTRY MONTH:
198706
YEAR OF PUBLICATION:
1983
SECONDARY SOURCE ID:
RISKLINE/1987050008
DOCUMENT NUMBER:
RISKLINE/1987050008
didgood.com © 10-Oct-2006